SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs141103375 | snp | C/T | 0.125515 | 0.216803 | intron-variant | KLHL13 | GRCh38.p7 | X:117984243 | TTTAAAAATAGAGAC[C/T]ACTACAGAAGCACTA | 90293 |
rs141106423 | snp | A/G | 0.126889 | 0.217586 | intron-variant | KLHL13 | GRCh38.p7 | X:118022320 | CACAGATATCTCGAG[A/G]AAGTGCTAATTCCAT | 90293 |
rs141129133 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978682 | TTATGACTAACTTTA[C/T]TCCTTCACTAAGGCT | 90293 |
rs141137082 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:118074771 | TTGATAAGATTTTCT[C/T]AGGTTTGTGAGGCTG | 90293 |
rs141163510 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117924424 | ACTCATAAATCTTTT[A/C]CCCTATTTAAGAAGC | 90293 |
rs141164024 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:117967720 | AATATTTTTCTGTTA[C/T]ATTAAATGATTTCAA | 90293 |
rs141200375 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117934655 | ATCTAGAATACATAT[A/G]TATGTAAAATATATA | 90293 |
rs141211395 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117947326 | CACAGAGCCTAGCAC[A/G]AAAGACTTAATATAT | 90293 |
rs141224877 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905347 | CTTATATGACACAAT[C/T]TTGAAAGATGCCAGA | 90293 |
rs141230321 | snp | A/T | 0.163039 | 0.234388 | intron-variant | KLHL13 | GRCh38.p7 | X:117942772 | CACCGATGGGCCTTG[A/T]CTATCCAATTTGCCA | 90293 |
rs141279565 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117913710 | TAGCCGGACGTGGTG[G/T]CACACGCCTGTATTC | 90293 |
rs141281681 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117998176 | ACATAGGTACACAGA[A/G]ACCCCATGGGAAGAA | 90293 |
rs141281834 | snp | A/G | 0.0271702 | 0.113344 | intron-variant | KLHL13 | GRCh38.p7 | X:117908730 | ATGGAAAAGAAAACT[A/G]TCTGATATTACGTCA | 90293 |
rs141360551 | snp | A/T | 0.0797195 | 0.183042 | intron-variant | KLHL13 | GRCh38.p7 | X:117970022 | AGCCTTCACTAGCAC[A/T]GCAGTACTGCCCTAT | 90293 |
rs141385825 | snp | C/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:117917386 | CTTCTCCATTAGAAA[C/T]AGGTTTTAGGATGTC | 90293 |
rs141407952 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118084792 | AGCACTTTGGAAGGC[C/T]GAGGCGGATGGATCA | 90293 |
rs141446330 | snp | C/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118094407 | AAAAGACCAAATCTA[C/G]GTCTGATTGGTGTAC | 90293 |
rs141463931 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:117988414 | TTCAGAGCAGGATGA[C/T]TTAAGTGGTTTACAG | 90293 |
rs141466199 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118109537 | TTGTTTAAAGATTTT[C/T]AAATAGCTACCAGTT | 90293 |
rs141473323 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117939421 | GCATGTGTCTTAACA[A/G]TAGAATGATTTATAA | 90293 |
rs141516117 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118080378 | TATGCATTCAACAAA[C/T]GTCTATTATCCAGAA | 90293 |
rs141557686 | snp | C/T | 4.5622e-05 | 0.00477587 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909659 | GTGAGTGGTGTCAGA[C/T]CTAATGGCAGTCCTG | 90293 |
rs141578184 | snp | C/T | 0.0209675 | 0.10022 | intron-variant | KLHL13 | GRCh38.p7 | X:118069287 | GCTCCATGCACGTTA[C/T]TGCCCTGAAGACCTT | 90293 |
rs141603133 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117947729 | TAACATTCAAAACAC[C/T]CCCTACTAATTTCTG | 90293 |
rs141634276 | snp | C/G | 0.13689 | 0.222949 | intron-variant | KLHL13 | GRCh38.p7 | X:117997260 | AAAAAAAGAGACTGA[C/G]TCATCAATTTTTAAA | 90293 |
rs141636337 | snp | C/T | 0.113499 | 0.209446 | intron-variant | KLHL13 | GRCh38.p7 | X:117961669 | AAAGGATTCAACCTG[C/T]TGTCGCTGGCCTTAA | 90293 |
rs141640386 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118025919 | GATGGAAAATGTTTA[C/T]ATTTGTGAGTAGAAG | 90293 |
rs141641784 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117937965 | AGATTTCTTTATTCT[A/G]GACATTTCATACAAA | 90293 |
rs141647191 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118066911 | ATTAAGGTACGTGCC[C/T]ATGAACACAATGAGA | 90293 |
rs141673547 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117901735 | GTCTCAAACTCCTGA[C/T]GCCTGAATTATTATT | 90293 |
rs141692497 | snp | C/T | 0.121377 | 0.214374 | intron-variant | KLHL13 | GRCh38.p7 | X:117929654 | GTTTTTTTAAAAAAG[C/T]AAACTCGCCAGATGT | 90293 |
rs141704768 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | KLHL13 | GRCh38.p7 | X:118014110 | GATTTTCAGGGAACA[A/G]GGGAAGATAACCATG | 90293 |
rs141721134 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118039075 | CCTGCTGCCTTGAAG[A/G]GAAGGACCCAGTCCT | 90293 |
rs141771658 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:117948892 | ATTTTACTGAAAGCA[C/T]TGTAAACGTGGTCAA | 90293 |
rs141802658 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101390 | CAATACAGATAACTG[A/C]GTTAGCCCCTGTCCT | 90293 |
rs141837142 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951001 | AGATGGTAGAAGCCA[C/T]TTTCCATTGGCTTTT | 90293 |
rs141870533 | snp | C/T | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118096583 | AACTCTTTGATGAGG[C/T]CAGCATCATCCTGAT | 90293 |
rs141887281 | snp | C/G | 0.0152462 | 0.0859689 | intron-variant | KLHL13 | GRCh38.p7 | X:117955950 | GTTACCATACTCCAA[C/G]AGTATATATGTGGTC | 90293 |
rs141905190 | snp | C/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118100715 | TGGCCCAATTTTTCT[C/G]TATTCTCTCTTACTA | 90293 |
rs141912385 | snp | C/G | 0.00098325 | 0.0221508 | missense | KLHL13 | GRCh38.p7 | X:117909885 | CGAAGCCAACGACAG[C/G]TAGCCTTAAAGAGCT | 90293 |
rs141930862 | snp | A/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118079968 | ACAGAAAACTCAGAA[A/T]TAAAGCCACACACCT | 90293 |
rs141954687 | snp | A/G | 0.105069 | 0.203703 | intron-variant | KLHL13 | GRCh38.p7 | X:118112716 | CCCCACAATATTAGG[A/G]TTTACTCCTATGGAA | 90293 |
rs141963048 | snp | C/T | 0.13689 | 0.222949 | intron-variant | KLHL13 | GRCh38.p7 | X:117996048 | TTCTGGGTGAACATA[C/T]GATAACTCTATGTTC | 90293 |
rs141966354 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118065727 | CCTGCCCTTGGCCTC[C/T]CTAGGCTCCATTAGG | 90293 |
rs142005165 | snp | C/G | 0.0338441 | 0.125605 | intron-variant | KLHL13 | GRCh38.p7 | X:117959388 | TTCAAATATTTTGTA[C/G]GTCCACCCAAACTAA | 90293 |
rs142032938 | snp | C/T | 0.0194105 | 0.0965841 | intron-variant | KLHL13 | GRCh38.p7 | X:117949451 | CAGTGAATCCCTCTG[C/T]AGAGGTTTAATTTGG | 90293 |
rs142047007 | snp | C/T | 0.0460406 | 0.14457 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117255 | GAGCAAAGGGTGTGC[C/T]CTGGAAGCGGTGCCA | 90293 |
rs142048493 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117978551 | ACTTTTTATAGTTGG[A/G]TGTCAGATGAAAGAG | 90293 |
rs142058790 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118041456 | CACTTAAGGCCAGGA[A/G]GTCTCGAGGCTACAG | 90293 |
rs142084941 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118061305 | TATTGAGAGAAACCA[C/T]GAGCATTTGGTGGGC | 90293 |
rs142103596 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118000160 | AGGTATTTACTATTG[C/T]CCTTACCCAAAACAG | 90293 |
rs142113635 | snp | A/G/T | 0.00019144 | 0.00978194 | stop-gained, synonymous-codon | KLHL13 | GRCh38.p7 | X:117910025 | GACGAAACTGTTAAC[A/G/T]TATTTATCCACTTCG | 90293 |
rs142114754 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117943515 | TATTTCTTGGAGGCT[C/T]TGTTCGTTTCTTTTC | 90293 |
rs142121493 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118101942 | TAAAACTCTTTCCTT[G/T]ATAAATTATCCAGTC | 90293 |
rs142125247 | snp | C/G | 0.0251071 | 0.109193 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029078 | TTTCAGGCATCCACT[C/G]GGGGTCTTGGAACAT | 90293 |
rs142149590 | snp | C/T | 2.28686e-05 | 0.00338139 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909530 | GATGCCATGCTGGTA[C/T]CTTGGGGCATCCATG | 90293 |
rs142153238 | snp | C/T | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118111823 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 90293 |
rs142156667 | snp | C/T | 0.111634 | 0.208218 | intron-variant | KLHL13 | GRCh38.p7 | X:117901053 | CATGTGCATAAAATA[C/T]AGATAATCAGCACAG | 90293 |
rs142173285 | snp | A/G | 0.0460406 | 0.14457 | intron-variant | KLHL13 | GRCh38.p7 | X:117962808 | AAATCACGTGGCCCT[A/G]AATCTGAATTTTGGC | 90293 |
rs142199833 | snp | A/G | 0.0194105 | 0.0965841 | intron-variant | KLHL13 | GRCh38.p7 | X:118114258 | TTTGAAATGTACATA[A/G]AATGAGAAAGAAGAT | 90293 |
rs142220837 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961154 | GCTCTAATAGGAGAA[A/T]CTTGTTTTCATGATA | 90293 |
rs142252523 | snp | A/G | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117919271 | TTAGACGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 90293 |
rs142256333 | snp | G/T | 0.0245906 | 0.108123 | intron-variant | KLHL13 | GRCh38.p7 | X:117981993 | TCAATCAACTTACTC[G/T]GCCTAGCCCAAAACC | 90293 |
rs142260226 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:118110817 | ACAAAAGACTCTCTT[A/G]TGCTAAAGAAGCATA | 90293 |
rs142264580 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118075984 | TTTTTTAAGTAAAAG[C/T]AAGTTTATTAAGAAA | 90293 |
rs142294135 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117969821 | TATAAGATGCTATTT[C/T]TACTAATATTGCCAC | 90293 |
rs142323027 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118026891 | TTTCAATGGAAAATT[C/T]TAAACAAGTAGGATC | 90293 |
rs142357152 | snp | C/T | 0.0240739 | 0.107039 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029176 | GGACCCTGTATGAAG[C/T]TGGGTTAGACAAGAG | 90293 |
rs142396013 | snp | A/G | 0.0535814 | 0.15466 | intron-variant | KLHL13 | GRCh38.p7 | X:118070307 | GTTTTGCTATGCAGT[A/G]TTTGTTATTGCTCAG | 90293 |
rs142420516 | snp | C/T | 0.11768 | 0.212112 | intron-variant | KLHL13 | GRCh38.p7 | X:117994768 | ACAGCAACTAGTGTC[C/T]AATATGTTCTCACTA | 90293 |
rs142451331 | snp | A/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117963131 | GATAAGTTACTTCAT[A/T]ACTCCATTGAACTAT | 90293 |
rs142488906 | snp | C/T | 0.0245906 | 0.108123 | intron-variant | KLHL13 | GRCh38.p7 | X:117982901 | ACATCCATTATCTTG[C/T]CCTCCCACACTCCAG | 90293 |
rs142495284 | snp | A/G | 0.125973 | 0.217065 | intron-variant | KLHL13 | GRCh38.p7 | X:118045124 | CATGCCTGTAATCCC[A/G]GCACTTTGAGAGGCC | 90293 |
rs142525134 | snp | C/T | 0.126889 | 0.217586 | intron-variant | KLHL13 | GRCh38.p7 | X:118015135 | CAAATTTCACACAGC[C/T]AGTAAGTAGCAGAGT | 90293 |
rs142565644 | snp | A/G | 0.11443 | 0.21005 | intron-variant | KLHL13 | GRCh38.p7 | X:117989422 | TGTATTAATATTTAT[A/G]TTAATATTCATTTTA | 90293 |
rs142569677 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118057243 | AGACTGTTCATTGAG[A/G]AGAGGAAAGTCTCTT | 90293 |
rs142576533 | snp | C/G | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:117918670 | TCAGGAACTGGGTGA[C/G]TATCATTAAGTACTC | 90293 |
rs142579121 | snp | A/G | 0.00172351 | 0.029305 | synonymous-codon, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117945569 | GTCTTCCTCTTCCAC[A/G]AGAGATCTGAAAGTT | 90293 |
rs142602588 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118099500 | TGAGTTAAGTCCAAG[G/T]GTACACAGCTATTAA | 90293 |
rs142639042 | snp | A/C | 0.118143 | 0.2124 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028846 | AAATATTAAACGGAG[A/C]ATTCTCAAAATAAAC | 90293 |
rs142643704 | snp | A/T | 0.0409784 | 0.137149 | intron-variant | KLHL13 | GRCh38.p7 | X:118091870 | TCAGACATAAAATGG[A/T]ATGAAATAATGGCAT | 90293 |
rs142648577 | snp | C/G | 0.0240739 | 0.107039 | intron-variant | KLHL13 | GRCh38.p7 | X:117921903 | TATACATTATACATA[C/G]ACTTTAAAACAAGAT | 90293 |
rs142674895 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941749 | ATTAATCTGGCTAGC[A/G]GTCTATCTATTTTGT | 90293 |
rs142679577 | in-del | -/ATTT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070758 | ATTTTTATTTATTTA[-/ATTT]TTTATTTATTATTAT | 90293 |
rs142692095 | snp | A/T | 0.0323082 | 0.122924 | intron-variant | KLHL13 | GRCh38.p7 | X:118107158 | ACATTATCCTGCATA[A/T]CCCTTTTCCTTCAAA | 90293 |
rs142709750 | snp | A/G | 0.163039 | 0.234388 | intron-variant | KLHL13 | GRCh38.p7 | X:117943814 | TGTTACCTACCTTCT[A/G]AAGCCTACTTCTGTC | 90293 |
rs142713950 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118006270 | ACATGGACTGTACAA[C/T]AGTGAAAGTCTAACA | 90293 |
rs142744714 | snp | A/G | 0.00554255 | 0.0523503 | intron-variant | KLHL13 | GRCh38.p7 | X:117910140 | CATGACTACTTTCAT[A/G]GCAATCACATCTTGA | 90293 |
rs142759875 | snp | C/G | 0.111634 | 0.208218 | intron-variant | KLHL13 | GRCh38.p7 | X:117949859 | CACTTAACTTTTCTT[C/G]GTAGAGAGGTTATGT | 90293 |
rs142765926 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118013595 | ACTAAAGGAAACTAA[A/G]CCAATGTGACAAACA | 90293 |
rs142823895 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117915799 | GTTCCGTGGGGCAAA[C/T]GCTAGATGCTAAAAA | 90293 |
rs142831534 | snp | G/T | 0.0343555 | 0.126481 | intron-variant | KLHL13 | GRCh38.p7 | X:118033028 | AAATGAAGTGAGAAG[G/T]GAAGTTTAGAGAAAA | 90293 |
rs142852075 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117980792 | ATCTAAAAATAAAAG[C/G]TTTTGACCAAATAAT | 90293 |
rs142895340 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118038697 | TAAAGCGCTCTGGCA[C/T]TCTAAATAAAGTGAG | 90293 |
rs142906630 | snp | A/G | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117954445 | ATAAAGGGATACATG[A/G]ATGGATGAATGGTAG | 90293 |
rs142922127 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029836 | AGCTGGGCATGGTGG[C/T]ATGTGCCTGTAGACC | 90293 |
rs142949872 | snp | C/T | 0.0414859 | 0.13792 | intron-variant | KLHL13 | GRCh38.p7 | X:118086297 | CAATAGTGGGACTGA[C/T]AGACTGAATGGTAGA | 90293 |
rs142953020 | snp | C/T | 0.11443 | 0.21005 | intron-variant | KLHL13 | GRCh38.p7 | X:117956298 | TGGAAGGCAGACTGA[C/T]GATTTGGGGAGGGGC | 90293 |
rs142980980 | snp | C/T | 0.0297427 | 0.118265 | intron-variant | KLHL13 | GRCh38.p7 | X:118105369 | ACTACATGGATTTTA[C/T]TCCTAGTTCTTATAC | 90293 |
rs142981434 | snp | C/T | 0.127347 | 0.217844 | intron-variant | KLHL13 | GRCh38.p7 | X:117934333 | GTCATTATAAATAAA[C/T]TGAGGTTTATCAGAC | 90293 |
rs143015899 | snp | A/G | 0.10601 | 0.20437 | intron-variant | KLHL13 | GRCh38.p7 | X:118084597 | AACTTTTATCTCACA[A/G]TTGTACACAGAAATG | 90293 |
rs143026398 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117959117 | AATTGTATCTATCTA[C/T]ATGCTTCAGCAACAT | 90293 |
rs143032403 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118023105 | TTTTGCAAGTGGATA[C/T]ACAGTTTTCCCAGCA | 90293 |
rs143058649 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:118074211 | CAGAAATGTAGGTTC[C/T]ACCTAAGGGTTTGTT | 90293 |
rs143128598 | snp | C/T | 0.000433503 | 0.0147161 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899103 | AGAATACCCCCCAAC[C/T]ACATAGATTTTATTT | 90293 |
rs143132725 | snp | A/G | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118091435 | AAAGTCTCAGTAAAG[A/G]AATAGAAGATATAAA | 90293 |
rs143137986 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117989630 | TGCCAATTCCACAGA[C/G]TTCTCTTTCATCTAG | 90293 |
rs143195575 | snp | A/C | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118050000 | CTATAGGTATACACC[A/C]TACACCATGCAGTTC | 90293 |
rs143212317 | snp | G/T | 0.0220041 | 0.102557 | intron-variant | KLHL13 | GRCh38.p7 | X:118089233 | GTCAGAAGAGGCCCA[G/T]TGGAGAGCCAGGACT | 90293 |
rs143255559 | snp | G/T | 0.0152462 | 0.0859689 | intron-variant | KLHL13 | GRCh38.p7 | X:118056563 | AATACCTTTTTACCC[G/T]TTCAATTAATTTACA | 90293 |
rs143291660 | snp | A/T | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:117936788 | TCTATTCCCTGTGAG[A/T]CCTTCTCCATTTACC | 90293 |
rs143298997 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118022738 | TGTTAAGATATTAAC[C/T]CTCATCACATATATG | 90293 |
rs143322783 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118059778 | CTACACTGACCTACA[A/G]TATACCAGATGATGA | 90293 |
rs143323401 | snp | A/C | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118113741 | TACTTATTTTCATTG[A/C]TCTTACTACAGTCTA | 90293 |
rs143328327 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118089793 | ATTAAAAAAGTATCA[A/G]TAGGGCTGGGTGTGG | 90293 |
rs143330682 | snp | A/G | 0.246302 | 0.249973 | intron-variant | KLHL13 | GRCh38.p7 | X:118008884 | GTATCTACTTCATAA[A/G]GTTATTATGAGAATA | 90293 |
rs143360698 | snp | A/G | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:117913366 | ATGCAATTTACATAT[A/G]TAATAGAATACACAT | 90293 |
rs143372110 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118069888 | TCACTGACTGACACC[C/T]ATAACAACTTTCAGT | 90293 |
rs143372465 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117910592 | TTCCCTTTCACGTAA[A/G]TAGGCATCACTCATT | 90293 |
rs143378479 | snp | C/T | 0.0343555 | 0.126481 | intron-variant | KLHL13 | GRCh38.p7 | X:117971161 | ACCATCTCTAAAAAT[C/T]GACAAATCAGGGGCA | 90293 |
rs143404950 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118027058 | TGGTCACAAGCAAAA[C/G]TCACAACAACAGTTA | 90293 |
rs143433684 | snp | C/T | 0.0333324 | 0.12472 | intron-variant | KLHL13 | GRCh38.p7 | X:118085870 | TCATCCACTCATCAG[C/T]TGATGGTCACTTAGT | 90293 |
rs143442168 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118077405 | TTGTGGAGGGTGTGG[A/G]AGTATAAAAGTATAT | 90293 |
rs143466226 | snp | G/T | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:117947341 | GAAAGACTTAATATA[G/T]GTCCTCTGAATGAAT | 90293 |
rs143470075 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118110966 | TCCTATGACATGAGA[A/C]CCACACAGCCAGTCC | 90293 |
rs143475343 | snp | A/C | 0.0590711 | 0.161388 | intron-variant | KLHL13 | GRCh38.p7 | X:118110086 | TTTAGTTTAGTTAGA[A/C]AGGAAAAGGCTGTCA | 90293 |
rs143537362 | snp | C/T | 0.0312828 | 0.12109 | intron-variant | KLHL13 | GRCh38.p7 | X:117925014 | ATAGAGAGAGGTACA[C/T]ATCTAATACCAGGAA | 90293 |
rs143539990 | snp | G/T | 0.0126344 | 0.0784702 | intron-variant | KLHL13 | GRCh38.p7 | X:117988277 | TCATATAATAGTGAT[G/T]ATGATGACAGGATCA | 90293 |
rs143543660 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118107649 | AGGGAGATAAACAAG[G/T]CTCAGAGAGGTGAAG | 90293 |
rs143553060 | snp | C/T | 0.138243 | 0.22363 | intron-variant | KLHL13 | GRCh38.p7 | X:117942803 | GTCTGTGTCTTTTAA[C/T]TGGGGCATTTAGCAT | 90293 |
rs143562913 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118005861 | AAACTAAGACATGGG[C/T]CTAAAAATAGCTGGA | 90293 |
rs143562971 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118043471 | ATATCTGATGAACAT[A/T]GATGCAAAAATCCTC | 90293 |
rs143565060 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108649 | ATTTGTATACTATGC[G/T]GTAAATGAAAGCAGC | 90293 |
rs143621380 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117944856 | TTTCTACTGTGTTTC[C/T]GTCCCCTGCTTTTAT | 90293 |
rs143633689 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118105530 | GATGCACTTGGAAGG[A/G]TCCCAGGCTCATAAT | 90293 |
rs143677267 | snp | A/G | 0.0409784 | 0.137149 | intron-variant | KLHL13 | GRCh38.p7 | X:118100299 | GCTGCAGCTGCTACC[A/G]CGTTCTCAGTTACTT | 90293 |
rs143717578 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991575 | AGGTCCCCTCAACCC[C/T]CAGCCCCACCTTATC | 90293 |
rs143730624 | snp | C/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:118006893 | TGGGAAGGAGTATAG[C/T]AGTATACTTGAAAGC | 90293 |
rs143782918 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117925753 | TATATACTCTGACCC[A/G]TCTTATCAGGTTGTT | 90293 |
rs143783370 | snp | C/T | 0.0353775 | 0.128208 | intron-variant | KLHL13 | GRCh38.p7 | X:117943406 | AGTTCTCCTGGAGAA[C/T]ACCCTGAAGAGTATT | 90293 |
rs143788229 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118006012 | GTGTCATTAAATATA[C/T]GTTTAAGGCCATATA | 90293 |
rs143887091 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118101600 | CTCAAGGACAAAAAG[C/T]AGGCAGCAGTTTAGG | 90293 |
rs143953305 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:117906828 | TCATTTCAAATGGAA[C/T]AAAATATCAAATAAT | 90293 |
rs143974229 | snp | C/T | 0.125973 | 0.217065 | intron-variant | KLHL13 | GRCh38.p7 | X:117957257 | ATAATGGTCTTTATA[C/T]ATACTGTGATTGTAT | 90293 |
rs143977262 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | KLHL13 | GRCh38.p7 | X:118021992 | TGGTGGCCAGTGATG[A/G]TGAGCATTTTTTCAT | 90293 |
rs144007240 | snp | G/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117924263 | CTGACTATACACATT[G/T]TTGTGTACAAGAAGG | 90293 |
rs144010100 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118023918 | ATTTGTATATGCATG[C/T]AAGCAACGTTTTGCT | 90293 |
rs144030255 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118042556 | ATAACAAGAGAAATT[C/T]TGGAAACTGTACAAA | 90293 |
rs144033334 | snp | A/G | 0.0419931 | 0.138684 | intron-variant | KLHL13 | GRCh38.p7 | X:118020693 | AAGACACATGCACAC[A/G]TATGTTTATTGCGGC | 90293 |
rs144040781 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117926716 | GCAGATGAATTAAGA[A/G]AGAAAATCAGAATGC | 90293 |
rs144070988 | snp | A/C | 0.0323082 | 0.122924 | intron-variant | KLHL13 | GRCh38.p7 | X:118096414 | TAGACCAATAACAGG[A/C]TCTGAAATTGAGGCA | 90293 |
rs144071560 | snp | G/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117915407 | TATTTTGTCTCCAAC[G/T]CTTCATCACCTCCAG | 90293 |
rs144097407 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118006923 | CTAGTATTAATATAC[C/T]TTCCCCTTCATATCA | 90293 |
rs144151268 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | KLHL13 | GRCh38.p7 | X:117902926 | CACCAAGCTAAAAAC[A/G]AAATTTAATTTAGCA | 90293 |
rs144173007 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997843 | AAGTACCCCTGAAGG[C/T]ACCCACAAAGCTCTT | 90293 |
rs144221671 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117939024 | TATACACGTGCCATG[G/T]TGGCTTGCTGCACCC | 90293 |
rs144221750 | snp | C/T | 0.130086 | 0.219364 | intron-variant | KLHL13 | GRCh38.p7 | X:117977431 | GCTAACTGACTAGTA[C/T]AGTTTGTCACCAGTA | 90293 |
rs144225107 | snp | C/T | 0.0230396 | 0.104828 | intron-variant | KLHL13 | GRCh38.p7 | X:117953346 | ACTCATAGATGGGAA[C/T]TGAACAATGAGAAAA | 90293 |
rs144229796 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118016138 | GCTTCGTCTTAAAAA[C/T]ATAATTTTAGACTTT | 90293 |
rs144231560 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118039294 | CTCCTACAGTCCCCA[A/G]TTCTAGGCCTTGACT | 90293 |
rs144286709 | snp | A/T | 0.138243 | 0.22363 | intron-variant | KLHL13 | GRCh38.p7 | X:117942708 | TCCATCCCTTTATTT[A/T]GAGCCTATGTGTGTC | 90293 |
rs144323733 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118045420 | GGCAAACTATCTGAA[C/T]AGACATTTCTCAAAA | 90293 |
rs144359669 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117931857 | TTCTTGCCTTTTGTA[C/T]CTCATAGCATTTTTT | 90293 |
rs144385633 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118108439 | CCCTTTCTTCACTTG[C/T]CTTTTTCTTCTTCAT | 90293 |
rs144386308 | snp | C/T | 0.118143 | 0.2124 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030605 | TGTTGGGAGGTGGGG[C/T]CTAACAGGAGGTGTT | 90293 |
rs144392044 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118087346 | TATACCGAGGTGACA[C/T]CTAACTCTTTGAAAC | 90293 |
rs144405810 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118053166 | AAGGATTATAAAACA[C/T]GCTGCTATAAAGACG | 90293 |
rs144441355 | snp | A/C | 0.0230396 | 0.104828 | intron-variant | KLHL13 | GRCh38.p7 | X:117936572 | GCAGAAAATAAGTGG[A/C]CTCATCCATCTGCCC | 90293 |
rs144451728 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117998019 | GCTGCCTCACCAAGA[C/T]AGAAATTGAGACGCA | 90293 |
rs144458679 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118076709 | TTTGAAGGCCTTAAT[A/G]GAAAAATGACTGCTC | 90293 |
rs144464193 | snp | C/T | 2.29113e-05 | 0.00338455 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117945488 | GCGTGTAGGTCCTGC[C/T]TTGGAAGACTGCAAA | 90293 |
rs144468622 | snp | A/T | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:117970970 | CAACAACCAACAGTC[A/T]ACATGCAAGATCTAT | 90293 |
rs144528392 | snp | A/G | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118080771 | CTGGGTACATACCCA[A/G]AGGAAATTAGATCAT | 90293 |
rs144528593 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118091784 | TCCCAAATTGAATAT[A/G]CCCAAGAAAATCCAC | 90293 |
rs144568986 | snp | C/T | 0.0209675 | 0.10022 | intron-variant | KLHL13 | GRCh38.p7 | X:117915243 | GAAATATATGTACTA[C/T]GCAGGAAATCCTCAG | 90293 |
rs144670530 | snp | C/T | 0.00370173 | 0.0428621 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985983 | ACACATGATGTAAAG[C/T]AAATGATCAATGAAT | 90293 |
rs144676782 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:118047559 | TGGTGTGAAAGCTAT[C/T]GCAGTTTTTGCCATT | 90293 |
rs144680622 | snp | C/T | 0.0343555 | 0.126481 | intron-variant | KLHL13 | GRCh38.p7 | X:118085960 | ATTTTTTTTTTGAGA[C/T]GGAGTTTTGCTTTGC | 90293 |
rs144704330 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117949739 | TATCATTGCAAATAG[C/T]AGTTCATGTTATACA | 90293 |
rs144729454 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998218 | CATTGGATTTTGAGA[C/G]ATTTCCCTAAAAGAT | 90293 |
rs144739684 | snp | C/T | 0.0399626 | 0.135589 | intron-variant | KLHL13 | GRCh38.p7 | X:118068964 | CTCCTGGGGAACCCA[C/T]ACTTTGGCAGAACAG | 90293 |
rs144774306 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117926274 | GGATTTCAGACAGAG[G/T]TGCAGGGAGTGGGAA | 90293 |
rs144780203 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:117989011 | TTAAAATTTTTATCA[C/T]GTTAGTTTGGAAACA | 90293 |
rs144804442 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118104848 | AGCTCTGTGAGTATA[C/T]TAAACATTACTGAAT | 90293 |
rs144822512 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:117922055 | TTTTATTTTCCATTA[C/T]TAATTCGTCTGCTGT | 90293 |
rs144828874 | snp | C/T | 0.0399626 | 0.135589 | intron-variant | KLHL13 | GRCh38.p7 | X:118022416 | TGAGGAACTTCTATA[C/T]TGTTTACCATAATGG | 90293 |
rs144830679 | snp | A/T | 0.00949095 | 0.0682305 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985554 | ACTGCTGGCCAGATA[A/T]GAAAATGAGAAGCAC | 90293 |
rs144895075 | snp | C/G | 0.13689 | 0.222949 | intron-variant | KLHL13 | GRCh38.p7 | X:117987946 | TAATCTTCAAAAACA[C/G]GCAGTACTTGGGGGA | 90293 |
rs144896532 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118049816 | TTTAGGTCTAAACTC[C/T]TACCAAAAAGACTGG | 90293 |
rs144920693 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117953955 | AATCCTAGAAAATAA[C/G]TCAGATGAAATTTGG | 90293 |
rs144993154 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117903323 | TCTCTCTACTGACTT[C/T]CTTTTCCACTTACTT | 90293 |
rs145014022 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117908739 | AAAACTATCTGATAT[C/T]ACGTCAACAGAATTA | 90293 |
rs145022698 | snp | C/T | 6.86397e-05 | 0.00585791 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117901858 | CATCACTCCTCCATA[C/T]ACAGTTCCAGCATGG | 90293 |
rs145057555 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102944 | ACTCAAAATCCTCTC[A/T]CCTAAATTATGTGAT | 90293 |
rs145129042 | snp | A/G | 0.0302564 | 0.119217 | intron-variant | KLHL13 | GRCh38.p7 | X:118086557 | GAGAAATAAAAGAAT[A/G]AGGTAGGTATTTATG | 90293 |
rs145129209 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117937712 | ATACAATACATATTG[C/T]CTTGTTACATTTTTA | 90293 |
rs145165266 | snp | C/T | 0.0600656 | 0.162557 | intron-variant | KLHL13 | GRCh38.p7 | X:117900468 | TTTTTCTCAGAGGAG[C/T]TGGAGCTCTCATTAT | 90293 |
rs145168178 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118003006 | AATGTGGCACACTTG[A/G]CGAAGGGAAAATAAT | 90293 |
rs145204106 | snp | C/G | 0.0580755 | 0.160203 | intron-variant | KLHL13 | GRCh38.p7 | X:118102534 | TGCATATAATGCTGT[C/G]AGTACCTCATAGAAT | 90293 |
rs145215098 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118081828 | GAGTGAGAATATGCA[A/G]TATTTGTCTTTCCAT | 90293 |
rs145227281 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118005569 | TTGTGCTCCTCAACA[C/T]TGGAAGAGGAAAGCA | 90293 |
rs145285421 | snp | A/C/T | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:118063785 | GAATTCTTAATAAAG[A/C/T]ATTAAGCTAGATTTA | 90293 |
rs145348510 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118503 | GGTTCAAGTGGGGTT[A/G]CTTTATAATAAGTTT | 90293 |
rs145353464 | snp | A/T | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:118044896 | ACAAATGGGATCACA[A/T]CAAGTTAAAAAGTTT | 90293 |
rs145376891 | snp | C/T | 0.0240739 | 0.107039 | intron-variant | KLHL13 | GRCh38.p7 | X:118070275 | CCTGTAAGTTTTGCT[C/T]ACGCTGCACCTCACA | 90293 |
rs145388402 | snp | A/G | 0.118143 | 0.2124 | intron-variant | KLHL13 | GRCh38.p7 | X:118008798 | CTTATTTACTGTGTG[A/G]CCTTAGACAATTTAC | 90293 |
rs145421646 | snp | A/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:118105580 | TAGTCACTGGCTGCT[A/T]GGTAATAATATTAGT | 90293 |
rs145440874 | snp | A/G | 0.0384368 | 0.133195 | intron-variant | KLHL13 | GRCh38.p7 | X:118051269 | TTTATGGCCGGGTAC[A/G]GTGGCTCACACCTGT | 90293 |
rs145454073 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117965274 | GACTTTTTAATGATC[A/G]CCATTCTAAGTGGTG | 90293 |
rs145465213 | snp | A/T | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:118085319 | CATTTATATAACATG[A/T]CTAGAATAAGCAAAT | 90293 |
rs145487072 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117920576 | AGGAATAACACAAAA[G/T]TAAGACTAATTTAGG | 90293 |
rs145494182 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117983205 | GTAAAATAGGGAAAA[C/T]GCTGCTTTCCTTGCC | 90293 |
rs145498868 | snp | A/T | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:117951046 | AGTATTCATACTGCA[A/T]TGAATTCGAAAGATA | 90293 |
rs145563655 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | KLHL13 | GRCh38.p7 | X:117917389 | CTCCATTAGAAATAG[A/G]TTTTAGGATGTCTGC | 90293 |
rs145564614 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:117955407 | GTTTTAAGAAATATA[A/G]TTGGCAGCCCTAAGA | 90293 |
rs145567115 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118022481 | AGGGTTCTCTTCTCT[A/G]CATCCTCTCCAACAC | 90293 |
rs145577097 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118017902 | TGGAAGACTGAAACT[C/T]TGTCAGAGCATTACA | 90293 |
rs145608389 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118109273 | TACCCTTGAAATTGC[A/G]CAACAGAGAAAAACA | 90293 |
rs145613756 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118085613 | TTCTGAGATTCCAGT[A/G]TCCATGATATCACTC | 90293 |
rs145649556 | snp | G/T | 0.137792 | 0.223404 | intron-variant | KLHL13 | GRCh38.p7 | X:117923698 | TGTGCATCATGTATC[G/T]TCAGCTGTGTAATTT | 90293 |
rs145656367 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044434 | AAGTTACTCTGAGGA[-/A]AAAAAAAAAAAAAAG | 90293 |
rs145744379 | snp | A/G | 0.261904 | 0.249716 | intron-variant | KLHL13 | GRCh38.p7 | X:118033437 | tgggggccaatattc[A/G]acattcttaaagaaa | 90293 |
rs145745261 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974678 | GCAAAAAGACAAACT[A/G]CTATTTTCCTGTGAA | 90293 |
rs145757358 | snp | A/T | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:118038246 | GGCAATCAGAGCAAG[A/T]TGGCTGAATAGAAGC | 90293 |
rs145764593 | snp | C/T | 0.017851 | 0.0927731 | intron-variant | KLHL13 | GRCh38.p7 | X:118083838 | TGTACCCCATAAATA[C/T]GAACAATTATCATGT | 90293 |
rs145786815 | snp | A/G | 0.00949095 | 0.0682305 | | | GRCh38.p7 | X:118073758 | CTGTATGTCCAGCTT[A/G]CTTTTGTAACTTTTA | 90293 |
rs145815375 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978582 | GTTATGGGGCTAAGA[C/T]AGGAGCTGGGATGAG | 90293 |
rs145821879 | snp | A/T | 0.127347 | 0.217844 | intron-variant | KLHL13 | GRCh38.p7 | X:118041591 | AGTTAAAGTGTAGAG[A/T]TTTATTGGTTTTCTC | 90293 |
rs145842791 | snp | A/G | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:117966527 | CCCCATCAAGCTACC[A/G]ATGACCTTCTTCACA | 90293 |
rs145846215 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117977600 | CCTAGCCAGAGTTTG[C/T]ATGAACAGGCACTGT | 90293 |
rs145849509 | snp | A/T | 0.0414859 | 0.13792 | intron-variant | KLHL13 | GRCh38.p7 | X:118040333 | AGAATTCAAAATAGC[A/T]GTTTTGATGAACCTC | 90293 |
rs145879638 | snp | G/T | 0.0126344 | 0.0784702 | intron-variant | KLHL13 | GRCh38.p7 | X:117943536 | GTTTCTTTTCATTCT[G/T]TTTTCTTTGATCTTG | 90293 |
rs145899652 | snp | A/G | 0.12963 | 0.219114 | intron-variant | KLHL13 | GRCh38.p7 | X:117969974 | ATAGTCTTGCTGCTC[A/G]ATGTTTGCAGTAAGT | 90293 |
rs145905718 | snp | C/T | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117940 | TTTGGCTGTTTTTTT[C/T]TTCTTCTTCTTCTTA | 90293 |
rs145915322 | snp | C/T | 0.126889 | 0.217586 | intron-variant | KLHL13 | GRCh38.p7 | X:117933471 | CCACATATGGAAGAA[C/T]GAAATTAGTCTCTCA | 90293 |
rs146116796 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117934434 | TATATGTTTAGGGAA[C/T]AGTGAAAAATCCAAA | 90293 |
rs146153122 | snp | G/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118084694 | TATTTAGATAAATTA[G/T]AAAACATCCAAATGA | 90293 |
rs146171522 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118096629 | AGACACAACCAAAAA[A/G]GAGAATTTTAGACCA | 90293 |
rs146183227 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118061427 | CTTAACACAATAAAC[A/G]CCAGGAACTGTGTAT | 90293 |
rs146208287 | snp | C/T | 0.00364621 | 0.0425419 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909563 | GGCTAACGATTTCCA[C/T]TCATGGGCCTTTTCA | 90293 |
rs146218255 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117959922 | AGCAAGAAGGGAGTG[C/T]AGTTAGGTACAGAGG | 90293 |
rs146237078 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117948899 | TGAAAGCATTGTAAA[C/T]GTGGTCAAACCAAAC | 90293 |
rs146272445 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118101395 | CAGATAACTGAGTTA[G/T]CCCCTGTCCTCAAGG | 90293 |
rs146290561 | snp | A/C | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118111256 | ATGTTATGTAATACA[A/C]CATTAGGGTCTATGG | 90293 |
rs146302709 | snp | C/T | 0.125515 | 0.216803 | intron-variant | KLHL13 | GRCh38.p7 | X:118079228 | TAAGAAAAGATTCAG[C/T]CATCTCTAGCTAAAT | 90293 |
rs146320017 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:118013567 | AAAGATATAAATTAC[A/G]TTGGTCGAGGAAACT | 90293 |
rs146335588 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117915597 | ACATATCTCATTCTC[C/T]TGTTAAAAAATGCTT | 90293 |
rs146338653 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117976789 | AGTTAAAAAATACCT[C/G]TGAAATGCACAGTTC | 90293 |
rs146353219 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118059494 | CAATGATGACATCCA[C/T]TTTAAGCGATTTGGG | 90293 |
rs146374433 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118080750 | TTTGATTCAGCAATC[C/T]CATTACTGGGTACAT | 90293 |
rs146422794 | snp | C/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:118024144 | GTTATCATTCAGTTA[C/T]CTTGCCATTTACAAA | 90293 |
rs146440270 | snp | A/C | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:117927367 | GGTGGCAGATGCCTA[A/C]AACCCTGTAAAAGAG | 90293 |
rs146468123 | snp | A/C | 0.0245906 | 0.108123 | intron-variant | KLHL13 | GRCh38.p7 | X:118064553 | AACTGACATGACTCT[A/C]TTTTTGCTCCAGATA | 90293 |
rs146488482 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | KLHL13 | GRCh38.p7 | X:118058705 | AATAATAATCAATTG[C/T]AAAATGTCACTAAAA | 90293 |
rs146509286 | snp | A/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:118061574 | CAAATAAAGATGTTG[A/T]CTCAAAACTAAATTA | 90293 |
rs146527621 | snp | G/T | 0.11536 | 0.210647 | intron-variant | KLHL13 | GRCh38.p7 | X:118022195 | CCTTTTTAAAAGACT[G/T]AATAATATCCCATTT | 90293 |
rs146544843 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977455 | ACCAGTACCACCTCA[C/T]CAAATGAACTAATAT | 90293 |
rs146646605 | snp | A/C | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118035425 | catccctgggatgca[A/C]ggctggttcaatata | 90293 |
rs146662906 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117993203 | CAGAGGGGATGGTTA[A/G]GAGAGAGGGTGCGGG | 90293 |
rs146663043 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117955026 | TAATGCACCTTAGCA[C/T]AAGAGTCAAATTTTA | 90293 |
rs146691460 | snp | C/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118089701 | AGATCCAGAATCTTA[C/T]GATATAATGCCTAAA | 90293 |
rs146707492 | snp | A/G | 0.0292288 | 0.117303 | intron-variant | KLHL13 | GRCh38.p7 | X:117947185 | CGTTTAAAATTACAG[A/G]ATCAATTGGAAAAGT | 90293 |
rs146764816 | snp | A/C | 0.137341 | 0.223177 | intron-variant | KLHL13 | GRCh38.p7 | X:117989834 | TTAGAAGATACAGGT[A/C]ATGGGTTTGCTATCC | 90293 |
rs146768106 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118058000 | ATGATGAATACAAAG[A/G]GAAAGACAGGCACTG | 90293 |
rs146786024 | snp | A/C | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117969823 | TTGTGGCAATATTAG[A/C]AGAAATAGCATCTTA | 90293 |
rs146793572 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118108746 | CTTTGACACCATGAA[C/T]TGTGCTGCTTTAAGT | 90293 |
rs146804486 | snp | C/G | 0.0338441 | 0.125605 | intron-variant | KLHL13 | GRCh38.p7 | X:117972483 | TTTGCAATTCCTTAG[C/G]TATGCCTTTGTACTT | 90293 |
rs146849712 | snp | C/G | 0.11443 | 0.21005 | intron-variant | KLHL13 | GRCh38.p7 | X:118036346 | TGACTTCAAACTATA[C/G]TACAAGGCTACAGTC | 90293 |
rs146887964 | snp | C/T | 0.0261392 | 0.111294 | intron-variant | KLHL13 | GRCh38.p7 | X:118006000 | CTGGATGTAGATGTG[C/T]CATTAAATATATGTT | 90293 |
rs146906424 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118100029 | CATACTTTTTGTCTA[C/T]ACAAAGTCAAAATTT | 90293 |
rs146922661 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118109921 | GCTCATGCCTGTAAT[C/T]CCAATACTTTGGGAG | 90293 |
rs146927103 | snp | A/C | 0.114895 | 0.210349 | intron-variant | KLHL13 | GRCh38.p7 | X:118006457 | GACAAATGATCTCAC[A/C]TTTGAATATCAGATT | 90293 |
rs146943245 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118011076 | AGACACTGTCTCAAA[A/T]TAAATAAATAAATAA | 90293 |
rs147011723 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118112167 | TCGGAACACCAAACA[C/T]GTGAAAAGTAAAACA | 90293 |
rs147031311 | snp | A/G | 0.127804 | 0.218101 | intron-variant | KLHL13 | GRCh38.p7 | X:117959204 | TGTTTCCAGTTTCAC[A/G]AACTTTGTTTAGCTG | 90293 |
rs147032681 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118023174 | CCTTCCATTAATTAT[C/G]CCTCTTTACTGACAT | 90293 |
rs147033152 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | KLHL13 | GRCh38.p7 | X:118069317 | TCCAGTGAGATAAGA[C/T]GTGTAAGTGGAAGGC | 90293 |
rs147047329 | snp | C/T | 0.125973 | 0.217065 | intron-variant | KLHL13 | GRCh38.p7 | X:117961975 | TTTGGGAGGCTGAGA[C/T]GGGAGGATAGCTTGA | 90293 |
rs147080149 | snp | A/G | 0.0271702 | 0.113344 | intron-variant | KLHL13 | GRCh38.p7 | X:117916537 | CTGATGCTCTGTTAT[A/G]GAAAACTGGTATCTC | 90293 |
rs147081037 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117978437 | AGGAACACTAGGTAA[C/T]GGATCCAAAGGAGAA | 90293 |
rs147120598 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118065061 | ACTGCTGGATCGACA[A/G]GACGTTCACTATGTG | 90293 |
rs147124635 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100650 | ACTCGCCTACTTAAA[A/C]CTGCCAATGGTTTCC | 90293 |
rs147134683 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117938016 | AATCACATAAAACAC[A/G]GACTTTGGTGATTAG | 90293 |
rs147207182 | snp | A/G | 0.0343555 | 0.126481 | intron-variant | KLHL13 | GRCh38.p7 | X:117968383 | TGTTAAAAGGGGTTT[A/G]GACTTTCTAAATGAC | 90293 |
rs147209127 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030544 | GCTATGGTTTGAATG[C/T]GCCCCCAAAAAAGAA | 90293 |
rs147209460 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118078053 | TCTGTGTAACAACTT[C/T]TGTTTTAAAAGTTAC | 90293 |
rs147225728 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118032810 | GCTAAGGGAGGAAAT[G/T]CAAACCAAAGGCAAG | 90293 |
rs147254415 | snp | A/C | 0.0404706 | 0.136372 | intron-variant | KLHL13 | GRCh38.p7 | X:118091363 | AGTAGCCATCATAAA[A/C]ATGCTTCATTGAGCA | 90293 |
rs147257393 | snp | G/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117956176 | GTGTTTATCCATGGT[G/T]CAGTAATTCTAAAGA | 90293 |
rs147271805 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118087097 | AAACTATGCCCAAGC[A/C]TCCAAAGTTTAGGCA | 90293 |
rs147297665 | snp | C/G | 0.11443 | 0.21005 | intron-variant | KLHL13 | GRCh38.p7 | X:118021024 | GAGGGATAGCATTGG[C/G]AGATATACCTAATGC | 90293 |
rs147317939 | snp | C/G | 0.191549 | 0.243071 | intron-variant | KLHL13 | GRCh38.p7 | X:117903159 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGG | 90293 |
rs147346323 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:117944204 | TGCGTTGATCTTGCC[A/G]GGAGCTGCAGACCAG | 90293 |
rs147360624 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118107240 | TATATATTGGGCTAA[C/T]TGTATTAAAAACTGA | 90293 |
rs147363234 | snp | A/C | 0.0271702 | 0.113344 | intron-variant | KLHL13 | GRCh38.p7 | X:117910423 | ACCCCCACCCCCAAA[A/C]TACTGATAAAATTCC | 90293 |
rs147377336 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118104491 | ATACGAGTCTGGCTT[C/T]GCTATTTAGAACTAA | 90293 |
rs147419981 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | KLHL13 | GRCh38.p7 | X:118001751 | ATGCCTGTGGTCTCA[A/G]CTACTCAGGAGGCTG | 90293 |
rs147420746 | snp | C/T | 0.16867 | 0.236401 | intron-variant | KLHL13 | GRCh38.p7 | X:118038764 | CAAGTCCTGGTGTTA[C/T]GCTGGGCTCAAAGCC | 90293 |
rs147435084 | snp | G/T | 0.138243 | 0.22363 | intron-variant | KLHL13 | GRCh38.p7 | X:117941750 | TTAATCTGGCTAGCG[G/T]TCTATCTATTTTGTT | 90293 |
rs147510037 | snp | C/G | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118056725 | GGTAATAGGCCTTTA[C/G]AAGCTTAATGACATA | 90293 |
rs147526302 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118059846 | GGTTAAGAGCATGGG[A/C]CCTGCAAATAAGCTA | 90293 |
rs147526618 | snp | A/G | 0.126889 | 0.217586 | intron-variant | KLHL13 | GRCh38.p7 | X:118016565 | AAAATCTTGCATTAT[A/G]TACAATACAGGATAT | 90293 |
rs147539635 | snp | A/G | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:117956486 | CTCCTGGTCATTTAA[A/G]TGGGAATTTTAAATT | 90293 |
rs147542431 | snp | C/T | 0.0595685 | 0.161975 | intron-variant | KLHL13 | GRCh38.p7 | X:118020373 | TGCTGAAGTTGCGTA[C/T]CAGCTTAAGGAGATT | 90293 |
rs147596504 | snp | A/G | 0.0425 | 0.139441 | intron-variant | KLHL13 | GRCh38.p7 | X:117978453 | GGATCCAAAGGAGAA[A/G]ACAATAGGGGTGAGG | 90293 |
rs147612888 | snp | C/T | 0.126889 | 0.217586 | intron-variant | KLHL13 | GRCh38.p7 | X:117965020 | GGTTTCAAGTCTTTG[C/T]TATTGTGAATAATGC | 90293 |
rs147621119 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118081868 | ATTTCACTTAACATA[A/G]TGACCCCCAGTTTTA | 90293 |
rs147637409 | snp | A/C | 0.085528 | 0.188279 | intron-variant | KLHL13 | GRCh38.p7 | X:118116418 | GCCCCTGGTACAGAT[A/C]GCAACTCCTCGCCGC | 90293 |
rs147645056 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117936305 | TCCTGGAACTTGTTC[A/G]AGATTCTAGGAATCC | 90293 |
rs147685497 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029170 | ACCTAAGGACCCTGT[A/G]TGAAGTTGGGTTAGA | 90293 |
rs147702421 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030625 | CAGGAGGTGTTTAGC[C/T]ATGGGGGCACCACCC | 90293 |
rs147708702 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118102004 | AACTAATACAAGTAG[C/T]AAGTACAAATGTGTG | 90293 |
rs147714787 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:117920186 | AAAAGATTTAAACAC[A/G]GATTTTTCATATTGT | 90293 |
rs147724824 | snp | A/C | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118099465 | AAGGCTAAGTTAAAG[A/C]CAGCCATGGGTTAAA | 90293 |
rs147731133 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117923739 | CCATATTCCATTCAA[A/T]CTGCTTGTGGAGGTA | 90293 |
rs147790519 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118045446 | CAAAAGAAGACATAC[A/C]TATGGCAAACAGGCC | 90293 |
rs147804959 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117947186 | GTTTAAAATTACAGA[A/G]TCAATTGGAAAAGTC | 90293 |
rs147807171 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118008964 | ATTTAAGTGTTAGCT[A/G]TTATAATGACTCTTG | 90293 |
rs147807333 | snp | A/G | 0.125973 | 0.217065 | intron-variant | KLHL13 | GRCh38.p7 | X:118048637 | TTCTGCCCTGAAGTC[A/G]GGACTATGTAGATGT | 90293 |
rs147819954 | snp | A/G | 0.137792 | 0.223404 | intron-variant | KLHL13 | GRCh38.p7 | X:117936634 | TACCCTCACTGTTCT[A/G]CTCTGTCTAGGTGAG | 90293 |
rs147822728 | snp | A/C | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117998031 | AGACAGAAATTGAGA[A/C]GCAGGGAAGCCAAAA | 90293 |
rs147836073 | snp | C/T | 0.0343555 | 0.126481 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897587 | GTGGTGATGAAAAGC[C/T]AGTTAGCATCTTCCA | 90293 |
rs147896605 | snp | A/C | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118069001 | CTTCTCCCAGCCATG[A/C]CTGCACCCTGCCCCT | 90293 |
rs147911606 | snp | C/T | 0.0152462 | 0.0859689 | intron-variant | KLHL13 | GRCh38.p7 | X:117961529 | AGGAGACTTTGAAAA[C/T]GTGATAAAGGTTACG | 90293 |
rs147913400 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:118072667 | CATCAAAAAGTGGGC[A/G]AAGGACATGAACAGA | 90293 |
rs147979899 | snp | C/T | 0.0353775 | 0.128208 | intron-variant | KLHL13 | GRCh38.p7 | X:117947623 | TGCCAACATAATATG[C/T]TTGCCTTTTTAATTA | 90293 |
rs148019971 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080344 | ACAACCTACAGAATG[A/G]GAGAAAATACTTGCA | 90293 |
rs148032932 | snp | G/T | | | missense | KLHL13 | GRCh38.p7 | X:117901944 | TGTAACATTCTACTG[G/T]GGCTGTTAAAAAAAA | 90293 |
rs148068946 | snp | C/T | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:117984128 | TCCTAACCAGAAGAT[C/T]TGGTTTTTGTTAAGT | 90293 |
rs148085287 | snp | A/G | 0.000182978 | 0.00956325 | missense | KLHL13 | GRCh38.p7 | X:117909880 | CCAGGCGAAGCCAAC[A/G]ACAGGTAGCCTTAAA | 90293 |
rs148108004 | snp | C/T | 0.0240739 | 0.107039 | intron-variant | KLHL13 | GRCh38.p7 | X:118059064 | CACTAAGGCATGACA[C/T]AGAAGAAAATGCAAA | 90293 |
rs148108465 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118100632 | ACATACAAAAACTGT[A/G]TTACTCGCCTACTTA | 90293 |
rs148122347 | snp | A/C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117955909 | CACTGTTACTTACAG[A/C/T]CCACTCACCTATCTA | 90293 |
rs148124606 | snp | C/G | 0.0245906 | 0.108123 | intron-variant | KLHL13 | GRCh38.p7 | X:118018333 | ATGAGTAGAAGAACT[C/G]ATCACTTTTCATCAT | 90293 |
rs148137789 | snp | C/T | 0.138243 | 0.22363 | intron-variant | KLHL13 | GRCh38.p7 | X:117943502 | TCATATAGTCCCATA[C/T]TTCTTGGAGGCTTTG | 90293 |
rs148161951 | snp | C/T | 0.0230396 | 0.104828 | intron-variant | KLHL13 | GRCh38.p7 | X:118065491 | AACTAATTATATATA[C/T]TATCTCTCCTGGGAA | 90293 |
rs148169439 | snp | C/T | | | missense | KLHL13 | GRCh38.p7 | X:117920313 | AAGCATCATCTGTGT[C/T]ACCTGGCATCAGGGT | 90293 |
rs148176677 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117959271 | TGTAGGAAAGTGATC[A/G]TAACGAATGAGAAAA | 90293 |
rs148190540 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117917217 | TACTCTAAAACCATA[C/T]AGACATATCCTCTGC | 90293 |
rs148194048 | snp | A/C/T | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:117978623 | TACAGAGAGACTGAG[A/C/T]AGAGAACAAAGATCC | 90293 |
rs148195565 | snp | C/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:118004182 | ATGAACTCTATGGTA[C/T]TGGATTAAAATTGAA | 90293 |
rs148198249 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118074599 | GACCATGGCAAACAT[C/T]TTCCACTGGCGATTT | 90293 |
rs148212017 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:117967454 | AAGTCTCAACTAAAT[A/G]TTCTAAGTTTCAAGC | 90293 |
rs148231131 | snp | A/C | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118110235 | TAATCTTAATGATGT[A/C]AAGTTTACAGAGGAA | 90293 |
rs148245975 | snp | A/G | 0.0157677 | 0.0873799 | intron-variant | KLHL13 | GRCh38.p7 | X:117922525 | CATGTAGTCACATTG[A/G]GTAGGATGTAAACTT | 90293 |
rs148282927 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118014841 | TCTAATATTAAGACA[C/T]TGTTTGTACCACAGA | 90293 |
rs148318426 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118022867 | ATTTTTGTTTCTGTT[G/T]CCTAAGCTTTTGGGG | 90293 |
rs148354649 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118069962 | ATTTTTTATCTTTTA[A/T]ACCATATTTTACCAT | 90293 |
rs148355254 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118089798 | AAAAGTATCAATAGG[G/T]CTGGGTGTGGTGGCT | 90293 |
rs148367962 | snp | A/T | 0.12963 | 0.219114 | intron-variant | KLHL13 | GRCh38.p7 | X:117962617 | CACCACTTGACAGTA[A/T]GCAAGTAAAGCTTTC | 90293 |
rs148371066 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118027092 | TGGGATGATCAAGAC[A/G]TTTTGCTTGAGGATT | 90293 |
rs148383943 | snp | G/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117930629 | GAGAGAGCAGGACAA[G/T]AACACACTGAAGTGG | 90293 |
rs148399043 | snp | C/T | 0.000120862 | 0.0077728 | missense, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117945568 | GGTCTTCCTCTTCCA[C/T]GAGAGATCTGAAAGT | 90293 |
rs148436027 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117901649 | AGCTGGGATTACAGA[C/T]GTGCACCACCACACC | 90293 |
rs148441098 | snp | C/T | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:117989027 | GTTAGTTTGGAAACA[C/T]AGAAATAAGCTAAAT | 90293 |
rs148457363 | snp | C/T | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:118091833 | TGGAGATACACAACA[C/T]ACACACACCATGGAA | 90293 |
rs148457789 | snp | A/C | 0.00949095 | 0.0682305 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975320 | TAAAACATAAAGCAG[A/C]TATATATTATGTAGT | 90293 |
rs148474070 | snp | A/G | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:117941827 | GTTCCTCGTGTCTCT[A/G]TCTCCTTCAGTTCTA | 90293 |
rs148478092 | snp | C/T | 0.00528398 | 0.051128 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028841 | TCAAAAAATATTAAA[C/T]GGAGAATTCTCAAAA | 90293 |
rs148491663 | snp | C/T | 0.0245906 | 0.108123 | intron-variant | KLHL13 | GRCh38.p7 | X:117932735 | ATATATACCCAGTAA[C/T]GGGATTGCTGGATCA | 90293 |
rs148508924 | snp | C/T | 0.0152462 | 0.0859689 | intron-variant | KLHL13 | GRCh38.p7 | X:117949783 | GGTCAAATTTCATTG[C/T]CAAGGAAAAGGGAAC | 90293 |
rs148510823 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118086956 | TAAAACATAACCTTA[A/G]CAAATAAGGATGTTA | 90293 |
rs148513855 | snp | C/G | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118033545 | aagcaaatgctgaga[C/G]attttgtcaccacca | 90293 |
rs148543576 | snp | C/T | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118081570 | AGTTATCTATCACCT[C/T]AAACATTTATCATTT | 90293 |
rs148577771 | snp | A/G | 0.132815 | 0.220834 | intron-variant | KLHL13 | GRCh38.p7 | X:118105055 | GTTTAAAATAAACAC[A/G]CCCACACACATATAC | 90293 |
rs148596502 | snp | C/G | 0.127347 | 0.217844 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986224 | ACAAAAATTCCGTTG[C/G]AACTGAGGCTGAAGA | 90293 |
rs148629148 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117906829 | CATTTCAAATGGAAT[A/G]AAATATCAAATAATT | 90293 |
rs148630577 | snp | C/T | 0.0209675 | 0.10022 | intron-variant | KLHL13 | GRCh38.p7 | X:118101785 | TAGTTCTAATGAGAT[C/T]TGATGGTTTTATAAG | 90293 |
rs148649295 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117956866 | TTTACATCTTCAAAA[C/T]CCAATCTTTTCATAT | 90293 |
rs148664493 | snp | C/T | 0.0183711 | 0.0940641 | intron-variant | KLHL13 | GRCh38.p7 | X:117944643 | AAGGCAAATTTTCCT[C/T]ATCTTATTAAGGGTA | 90293 |
rs148667486 | snp | A/C | 0.114895 | 0.210349 | intron-variant | KLHL13 | GRCh38.p7 | X:118007032 | CTTATTAGACTTAGC[A/C]CTGCTTCAGGGAATC | 90293 |
rs148686446 | snp | G/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117997968 | TACAAAGCACTTTCA[G/T]GTCCTTGATTTCATT | 90293 |
rs148688337 | snp | C/T | 0.0343555 | 0.126481 | intron-variant | KLHL13 | GRCh38.p7 | X:118068028 | GCATCACCACAAACA[C/T]GTGAAGAATGCTTTG | 90293 |
rs148702918 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:117960751 | TTGGGAAGGTAGAAA[C/T]GTAGAGTCCTTTGAA | 90293 |
rs148718560 | snp | A/G | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117919262 | CTCCCAACCTTAGAC[A/G]ATCTGCCCGCCTCGG | 90293 |
rs148720512 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981835 | TTGAATGGATACTCT[A/G]AACAGGGAAAAAGCA | 90293 |
rs148724542 | snp | A/C | 0.0323082 | 0.122924 | intron-variant | KLHL13 | GRCh38.p7 | X:118075652 | CTGCCATTCCCAGTG[A/C]CATGGAATAAAAGAG | 90293 |
rs148740901 | snp | C/T | 0.126432 | 0.217327 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030633 | GTTTAGCCATGGGGG[C/T]ACCACCCTCATGAAG | 90293 |
rs148757224 | snp | A/C | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:118021688 | TATTGTGAATAGTGT[A/C]GCAATAAACATACGT | 90293 |
rs148770972 | snp | G/T | 0.0343555 | 0.126481 | intron-variant | KLHL13 | GRCh38.p7 | X:117923755 | CTGCTTGTGGAGGTA[G/T]GTAATCAATGCTCAA | 90293 |
rs148812440 | snp | C/T | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:118017867 | TTTTATACTGTGTTT[C/T]ATCTATGAAAGACTA | 90293 |
rs148829062 | snp | A/G | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:117983292 | GAAAATATAAGGCAC[A/G]ATACAATGATGCGTG | 90293 |
rs148833842 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052434 | AGGCTGAGGCAGGAG[A/G]ATGGCATGAATCTGG | 90293 |
rs148833977 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077275 | TGTGATCAATTCTAT[A/G]AGAGAAAGTTAAGCA | 90293 |
rs148863849 | snp | C/T | 0.11443 | 0.21005 | intron-variant | KLHL13 | GRCh38.p7 | X:117958708 | CAGGATACTTGCTTG[C/T]TAAGAGATGATAATA | 90293 |
rs148866092 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118022496 | ACATCCTCTCCAACA[C/G]TTGCTATCATTTGTC | 90293 |
rs148881461 | snp | G/T | 0.124138 | 0.216007 | intron-variant | KLHL13 | GRCh38.p7 | X:117925009 | ATTAAATAGAGAGAG[G/T]TACATATCTAATACC | 90293 |
rs148927471 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118100275 | GCTGGCAAAATAGCA[C/T]GGGCCGATGCTGCAG | 90293 |
rs148948871 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:117938906 | ACAAACAAAAATAGC[C/T]GAAGACTCGTTTTCA | 90293 |
rs148985275 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117978346 | TTCCTATCTGTAACA[C/T]TTCCTTAAGATAAGA | 90293 |
rs149005983 | snp | A/G | 0.11443 | 0.21005 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029390 | GACATAAAATAGCGG[A/G]TAGAAATATTTTCTT | 90293 |
rs149023083 | snp | C/T | 0.0348667 | 0.127349 | intron-variant | KLHL13 | GRCh38.p7 | X:118049944 | GAAGCAATCTGCCCA[C/T]GTCACCACCATGTGG | 90293 |
rs149038039 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117950818 | TCTGCTCTGAAACAG[A/G]GAAGTGTCTGCTAGC | 90293 |
rs149052634 | snp | A/G | 0.0261392 | 0.111294 | intron-variant | KLHL13 | GRCh38.p7 | X:117916847 | AGCCTATTTCCTCTA[A/G]AACATCTTATTTCAG | 90293 |
rs149074691 | snp | A/C | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:117991410 | TATAAACCAATCCCA[A/C]GCCAAGAGTAAACAT | 90293 |
rs149076607 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118058948 | ATGTTAGTAACTGAC[A/G]CACACCTTAGTCCTT | 90293 |
rs149091331 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117955761 | TGCATATCTGCCTCA[C/T]CATTAAGGGTTTTTT | 90293 |
rs149120919 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897459 | GACAAATCTCTAAGG[C/T]AATTTTACACAATCC | 90293 |
rs149159273 | snp | A/T | 0.0500702 | 0.150094 | intron-variant | KLHL13 | GRCh38.p7 | X:117969790 | TACAGCAAAATTTTT[A/T]AAGTGCTTTATACTA | 90293 |
rs149164446 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118063967 | GCAGCTGTTATATAT[C/T]TTTTTCCGACTAAGT | 90293 |
rs149199753 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:118079411 | AAAATCCACCAAAAC[A/G]CTACTAGAACTGATA | 90293 |
rs149213612 | snp | A/G | 0.0399626 | 0.135589 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973092 | AGCGTTGACTGCAGT[A/G]TATTTTTTTAGGACT | 90293 |
rs149218823 | snp | G/T | 0.0162933 | 0.0887759 | intron-variant | KLHL13 | GRCh38.p7 | X:118069774 | TAATTTATTACCAAA[G/T]AAAAAATATTTTTTA | 90293 |
rs149260705 | snp | C/T | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118080182 | AAGTGTAGAAGAAAA[C/T]CTATGAATACTCTTT | 90293 |
rs149269364 | snp | C/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:117970509 | AAACAATTGTGAGAA[C/T]AAATATAATGTTACT | 90293 |
rs149306319 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118012191 | AGTCAGAAATTACAG[C/T]TCCTGGTATATATTA | 90293 |
rs149319437 | snp | C/T | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:117914620 | GACCATCACAGGACA[C/T]AAAGAAGAGACACTT | 90293 |
rs149327068 | snp | A/G | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:118070540 | ATAAATGTTCTGTCC[A/G]TACTTGTGATAAGAC | 90293 |
rs149338296 | snp | A/C | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:117934094 | AAACATTGGGTACAC[A/C]TGGACACAAAAATGG | 90293 |
rs149396187 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118023872 | CCTTTTCCTATGTTT[C/T]ACTGTATTTGGAATT | 90293 |
rs149437196 | snp | C/T | 0.0580755 | 0.160203 | intron-variant | KLHL13 | GRCh38.p7 | X:118086710 | CATCTGTAAGCAAAG[C/T]AAATAAACAAAATGA | 90293 |
rs149466592 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038194 | CCAATTAAGTAACAA[A/G]TGAAGTGATGAGATT | 90293 |
rs149490873 | snp | C/G/T | 0.017851 | 0.0927731 | intron-variant | KLHL13 | GRCh38.p7 | X:118083584 | AGGCTGGGCGAGAGT[C/G/T]GGGGGCAGGTAATGA | 90293 |
rs149506967 | snp | A/G | 0.0323082 | 0.122924 | intron-variant | KLHL13 | GRCh38.p7 | X:118096413 | ATAGACCAATAACAG[A/G]CTCTGAAATTGAGGC | 90293 |
rs149516862 | snp | C/T | 0.130086 | 0.219364 | intron-variant | KLHL13 | GRCh38.p7 | X:117979496 | TGTATCTTCCTAATC[C/T]AGCACCATTCCTGGC | 90293 |
rs149519480 | snp | A/C | 0.11443 | 0.21005 | intron-variant | KLHL13 | GRCh38.p7 | X:118042281 | TAATAACCCATTTTC[A/C]GCATTGGACACATCA | 90293 |
rs149533542 | snp | A/G | 0.0245906 | 0.108123 | intron-variant | KLHL13 | GRCh38.p7 | X:117944578 | TGGTTCTTGATCAGG[A/G]ATATGCATGAAATCC | 90293 |
rs149538500 | snp | A/T | 0.0399626 | 0.135589 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030521 | ATGCAAATTTTCTCT[A/T]AATCTCTGCTATGGT | 90293 |
rs149555333 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118053063 | TGCAACATAGGCAAA[G/T]GTTTAATATTCATTA | 90293 |
rs149568492 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109839 | ACTGCAGAAAAAATC[A/C]TTTGAGACATGTAAT | 90293 |
rs149569615 | snp | A/C | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117952171 | CTACAAGACTACAGT[A/C]ATCAAAACAGCATGG | 90293 |
rs149586542 | snp | C/T | 0.163039 | 0.234388 | intron-variant | KLHL13 | GRCh38.p7 | X:117919086 | TGGAGTGCAATGGCG[C/T]GATCTCAGTTCGCCA | 90293 |
rs149608344 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118060678 | ACCATTGCTAAGTGG[C/T]TGAGTCAGAATTCTA | 90293 |
rs149656776 | snp | C/G | 0.129174 | 0.218863 | intron-variant | KLHL13 | GRCh38.p7 | X:117964641 | GTGCACAACGTGCAG[C/G]TTTGTTACATATGTA | 90293 |
rs149659838 | snp | A/G/T | 0.0164543 | 0.0893777 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028514 | TGTTCAGGAGGAAAA[A/G/T]AAGCCAATATTTACT | 90293 |
rs149678201 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118017662 | CACCCCATATGTCCT[A/T]TCAACAGCACTTAAG | 90293 |
rs149784493 | snp | A/G | 0.105069 | 0.203703 | intron-variant | KLHL13 | GRCh38.p7 | X:118079212 | GAATATCCGAGAAGC[A/G]TAAGAAAAGATTCAG | 90293 |
rs149830753 | snp | C/G | 0.127804 | 0.218101 | intron-variant | KLHL13 | GRCh38.p7 | X:117926130 | TTCGATTTACATTAC[C/G]TCCTGAAACTCTTTA | 90293 |
rs149851228 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117916293 | AAAGGCAATTTTCCA[C/T]TATCTTCATAGTATA | 90293 |
rs149867110 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117936071 | CAGTGAATTACCATA[C/T]GATAGGACAGTAAGA | 90293 |
rs149870538 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | KLHL13 | GRCh38.p7 | X:117997665 | GTAAGGTCCTTCAAG[A/G]TCAGATGATTCTCCT | 90293 |
rs149891379 | snp | C/T | 0.0455357 | 0.143855 | intron-variant | KLHL13 | GRCh38.p7 | X:118049721 | CTCATTTTAAGTACA[C/T]GATCAGCCTGCCTGG | 90293 |
rs149902444 | snp | C/G | 6.84127e-05 | 0.00584822 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899265 | GCCACCAATGACATA[C/G]AGCCTTTCTCCCACT | 90293 |
rs149925820 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118025501 | AGTTAGTAGATCAAC[C/T]GCTGAGGTATTTAGT | 90293 |
rs149961019 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118088193 | TTATTGTTAAAGCAG[A/G]TAGCCTTTTCCTCAA | 90293 |
rs149972683 | snp | A/C | 0.017851 | 0.0927731 | intron-variant | KLHL13 | GRCh38.p7 | X:117912800 | ATATTTATGGGGTAC[A/C]CAAGACTAAGTATTT | 90293 |
rs150030106 | snp | C/G/T | 0.0323082 | 0.122924 | intron-variant | KLHL13 | GRCh38.p7 | X:118099439 | GAAGCTATAAACTTA[C/G/T]AGACTTTCAAAAGGC | 90293 |
rs150043901 | snp | A/C | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117956670 | AACCAGTGTTTCACA[A/C]CCCAAACTATAATTT | 90293 |
rs150048523 | snp | C/G | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118108215 | GAATAGACTGTAAAA[C/G]CACTTCACCTGTAGA | 90293 |
rs150060921 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117946113 | CCCCCATTAATAAAA[C/G]TAAAAGATTAATTGT | 90293 |
rs150064009 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118008751 | CAAAGACTCTGGAGC[C/T]AGACTTCCTGCATTT | 90293 |
rs150113007 | snp | C/T | 0.00685808 | 0.058155 | intron-variant | KLHL13 | GRCh38.p7 | X:117920390 | AACAAGAACATGAGT[C/T]GAGTCACTAATCAAG | 90293 |
rs150118001 | snp | C/G | 0.114895 | 0.210349 | intron-variant | KLHL13 | GRCh38.p7 | X:118006168 | GAAAAGAAACTACTG[C/G]AACTATTTAGATAAG | 90293 |
rs150134588 | snp | A/G | 0.0183711 | 0.0940641 | intron-variant | KLHL13 | GRCh38.p7 | X:117994380 | CACCTTAGTCTTCTG[A/G]GTAGCTGAGACTACA | 90293 |
rs150155372 | snp | A/G | 0.0220041 | 0.102557 | intron-variant | KLHL13 | GRCh38.p7 | X:118046792 | GAAAACAGAGAGAAC[A/G]GTAGGAGGGAAACTA | 90293 |
rs150170173 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:117947758 | TGCTTTGGTAACAGT[A/G]CATGCCATGTTAACC | 90293 |
rs150185964 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117965558 | AACTCATTTGATGAG[A/G]CCAGCATCATCCTGA | 90293 |
rs150202074 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | KLHL13 | GRCh38.p7 | X:117933919 | GTACCATCCATTTAA[A/G]ATGGATCATATACAC | 90293 |
rs150206962 | snp | A/T | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118019091 | ACTTCCTTGGAAAAT[A/T]TTCAGAATAGAATAT | 90293 |
rs150238128 | snp | A/G | 6.8408e-05 | 0.00584802 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909782 | ATCCACCGTTTGCAC[A/G]TAATTAATGAGCTCC | 90293 |
rs150307676 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118083245 | GCAATCACAATTCCA[A/G]GTATATATATGTATC | 90293 |
rs150360930 | snp | C/T | 0.114895 | 0.210349 | intron-variant | KLHL13 | GRCh38.p7 | X:117990556 | ATTAAATTACTGTTG[C/T]TACAAGTCATGACGA | 90293 |
rs150412518 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898692 | GTTAAACATCAGCTT[A/C]TATGGGATACATTTC | 90293 |
rs150483931 | snp | A/G | 0.0110639 | 0.0735497 | intron-variant | KLHL13 | GRCh38.p7 | X:118089958 | TGGTGGCGTGTGCCT[A/G]TAGTCCCAGCTACTC | 90293 |
rs150501476 | snp | C/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:117914186 | TTTAAAAGATTGGTG[C/T]TTTATACAAAGAAAT | 90293 |
rs150509029 | snp | C/T | 0.127804 | 0.218101 | intron-variant | KLHL13 | GRCh38.p7 | X:118070346 | AGTTTACATTTCTAT[C/T]AGGATTTCTTTCACC | 90293 |
rs150520097 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117902166 | ATTAGACTAGATAGT[A/G]TAAGAATCTAACAAA | 90293 |
rs150560689 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:118005032 | AAAAACACTAAAAAG[A/G]CATTACAATTAATTG | 90293 |
rs150587373 | snp | C/T | 0.105069 | 0.203703 | intron-variant | KLHL13 | GRCh38.p7 | X:118091995 | ATTCTCACTCATATG[C/T]GGGAGCTAAGCTATG | 90293 |
rs150621964 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115713 | CTCTCAGGCCTGCTC[A/T]GCAGCCAGGGAAGAA | 90293 |
rs150643927 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117922911 | TCTATATATCATAAT[A/C]TACATTATGCTTGTA | 90293 |
rs150645756 | snp | A/G | 0.0147244 | 0.0845304 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985915 | CTCCCTGCATTGCCC[A/G]TCTTCAATTTGTCAA | 90293 |
rs150647950 | snp | A/C | 0.114895 | 0.210349 | intron-variant | KLHL13 | GRCh38.p7 | X:118007694 | AAACATCTTTACCTT[A/C]AGGATCATGCATTTC | 90293 |
rs150648626 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117924708 | TTATCTTAGTTCTCT[A/G]CTTTTCTGTCTCTGT | 90293 |
rs150649930 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118078610 | TTGTTCCTTTTTATT[A/G]TTAAGTAGTATATTT | 90293 |
rs150679431 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117959510 | TAAGATTTTGTAGAG[A/C]TGGTCTTTAATATTA | 90293 |
rs150683818 | snp | A/G | 0.0348667 | 0.127349 | intron-variant | KLHL13 | GRCh38.p7 | X:118048010 | GTGTAGTGACAGAGA[A/G]GCAACTGGAGACCTT | 90293 |
rs150700481 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118013705 | ATTATAACAGATATG[G/T]AAGGCACTACTACAA | 90293 |
rs150715516 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117967760 | TTAAAAAATACACAA[C/T]AGGCTTTAAAACAAA | 90293 |
rs150717008 | snp | C/T | 0.0147244 | 0.0845304 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030214 | TTCTGCTTATAATTC[C/T]GTTATTACAAGTAAA | 90293 |
rs150730346 | snp | C/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:117935293 | CAGAAAGGAAGGAAG[C/T]ATGTTATATGCCACA | 90293 |
rs150765407 | snp | A/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:117911500 | GGTTTGCTGCACCTA[A/T]CAACCCGTCATCTAC | 90293 |
rs150806222 | snp | C/T | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118074832 | CCCAACATGTGCACA[C/T]TGAATTATCCCTCCC | 90293 |
rs150859014 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118039278 | TAAAGGACCAAGCAG[C/G]CTCCTACAGTCCCCA | 90293 |
rs150875231 | snp | G/T | 0.017851 | 0.0927731 | intron-variant | KLHL13 | GRCh38.p7 | X:118027146 | TCATCTGTTTATTAT[G/T]AGAGTGTTTTGAGAA | 90293 |
rs150910866 | snp | C/G | 0.127347 | 0.217844 | intron-variant | KLHL13 | GRCh38.p7 | X:117982101 | TACAAATACACAAAA[C/G]AACACATGTTCCCTG | 90293 |
rs150936625 | snp | C/T | 0.0850455 | 0.187856 | intron-variant | KLHL13 | GRCh38.p7 | X:118085877 | CTCATCAGCTGATGG[C/T]CACTTAGTTTGATTC | 90293 |
rs150949209 | snp | A/C | 0.0384368 | 0.133195 | intron-variant | KLHL13 | GRCh38.p7 | X:118057384 | AAAACCTGTTAAGAG[A/C]TAAAACTCTTAGATA | 90293 |
rs150950647 | snp | A/G | 0.000138424 | 0.00831823 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972752 | GCTGGAGAAAGTGGA[A/G]TTGACCTGGATGTTT | 90293 |
rs150955239 | snp | G/T | 0.0323082 | 0.122924 | intron-variant | KLHL13 | GRCh38.p7 | X:118098500 | AACTAGTTCAACCAT[G/T]GTGGAAGACAGTGTG | 90293 |
rs150968013 | snp | G/T | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:118040860 | CCAATACATCTGTCA[G/T]CAGGCTTTTCAGTGG | 90293 |
rs150971356 | snp | C/T | 0.0338441 | 0.125605 | intron-variant | KLHL13 | GRCh38.p7 | X:118109097 | TTGGGATAACAGGAG[C/T]GAGCCACTGCGTCAG | 90293 |
rs150984070 | snp | G/T | 0.118143 | 0.2124 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029062 | TCGGTACTCTCCACG[G/T]TTTCAGGCATCCACT | 90293 |
rs150996571 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117907834 | AAAGATCAGGAAAAA[G/T]ACCATGTCACTAACA | 90293 |
rs150997205 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117933366 | AAATCCATGTATTTA[C/T]AGCCAAGTGATTTTT | 90293 |
rs151000644 | snp | A/T | 0.0419931 | 0.138684 | intron-variant | KLHL13 | GRCh38.p7 | X:117994078 | CCTGTTTCTAATTTC[A/T]AAAGCAAATTTTGCT | 90293 |
rs151032474 | snp | A/G | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117916070 | GGCTGAGGCAGGATA[A/G]TCGCTTGAACCTGGG | 90293 |
rs151035814 | snp | C/T | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118002808 | ATTTCAAAATATAAA[C/T]AATTCTAAATTATGA | 90293 |
rs151038513 | snp | C/T | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:118073012 | GGTGGGAGAATTGCT[C/T]GAGCCCTGGAGGTCA | 90293 |
rs151147608 | snp | C/T | 0.103183 | 0.202348 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117272 | TGGAAGCGGTGCCAC[C/T]TCACCTCAGTGGGGC | 90293 |
rs151160317 | snp | A/G | 0.114895 | 0.210349 | intron-variant | KLHL13 | GRCh38.p7 | X:118021773 | TAGGATGGCTGGGTC[A/G]AATGGCATTTCTGGT | 90293 |
rs151173360 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117924020 | AGGTTTTACATTTAT[C/T]TTCACAACATACAGT | 90293 |
rs151196763 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | KLHL13 | GRCh38.p7 | X:118068480 | TCACCCCATCCCCCA[C/T]GTGAGATAACCTGGG | 90293 |
rs151210855 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117961184 | ATTTTCAACACAACC[A/C]CAGATTATAGTTCTG | 90293 |
rs151228350 | snp | A/T | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:117928686 | ATTGTGGAGTGCAGA[A/T]GAAGCTCTACTTAGG | 90293 |
rs151228729 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118116908 | ACATGGCGGCGGGGG[G/T]GGCCCCGGCGGCGCC | 90293 |
rs151244257 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117945366 | CACTACTGACATCCT[C/G]CATCACAAAATCCAT | 90293 |
rs180673074 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118021979 | ATTTGTATTTATCTG[A/G]TGGCCAGTGATGATG | 90293 |
rs180673980 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987161 | AAGGGATACCGACAG[A/G]AGAGCTGAATGATGG | 90293 |
rs180680029 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002559 | GATCGCACCATTGCA[C/T]TCCAGCCTGGGCAAC | 90293 |
rs180682652 | snp | A/C | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:118035360 | AAAATACTGGCAAAC[A/C]AAACCCAGCAGCACA | 90293 |
rs180694886 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017810 | AATATGATTGTACAG[G/T]GTTTGGCACTCTTTC | 90293 |
rs180699639 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030765 | TTCCAACTTCTGCCA[C/T]GGGATGACACAGCAA | 90293 |
rs180838720 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912164 | TCACTTCCCAAGACA[A/G]GTAAGAATTATCTCG | 90293 |
rs180857907 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925591 | GGACATAAATGTTTA[C/T]ATTAATTTTAAACTC | 90293 |
rs180859588 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118096234 | AGACACAATACAAAA[C/T]GACAAAGGGGGTATC | 90293 |
rs180870960 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117944030 | GTGGATGCCATTTTT[A/G]TTGTTCTTGATGCTA | 90293 |
rs180879228 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064771 | TAAATGCTAGCCTCA[C/T]TACATATTTGCTAGC | 90293 |
rs180894352 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111105 | CACCCACAGCAACAA[C/T]ATACTATGTGCAAGG | 90293 |
rs180897160 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117935157 | AAAACATGTCCTCAC[A/G]GACATTTACACATGA | 90293 |
rs180900351 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117959733 | CCTGATTAAGATAAT[C/T]ATGCACATTATATGA | 90293 |
rs180904647 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117990727 | GCAAAATATACAAAT[G/T]ACACACAAGAGGGCC | 90293 |
rs180907129 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118081740 | AACCTCTCTTCATTC[C/T]TCCTGCTACCCTTCC | 90293 |
rs180922937 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117966919 | TTAATTCAAGATGGA[C/T]TGAAGACTTAAATGT | 90293 |
rs180934878 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118048590 | TTGGAATTTTCTAAT[A/G]AAGAAGAAACAAAAA | 90293 |
rs180937594 | snp | C/T | 0.00236267 | 0.0342892 | intron-variant | KLHL13 | GRCh38.p7 | X:117983593 | ATTGTAGTTTTATTA[C/T]ATTTAGTTCAAATTT | 90293 |
rs180938671 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117999325 | GAGACTGGATTAAGA[A/C]AATGTGGTACATATA | 90293 |
rs180941016 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019442 | TCCCATTTTGTAGGT[G/T]GCCTGTTCACTCTGG | 90293 |
rs180943497 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974726 | ACATGCAGTATGTAC[A/G]TATACACATACATAC | 90293 |
rs180949959 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118014354 | GACTGAAATACACCC[C/T]GGTCTCCTGCAGTGC | 90293 |
rs180958204 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027012 | ATGGCTAGGAAAAGG[C/T]AGAAGTAACCCAGTC | 90293 |
rs180966064 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040278 | ATGAGGTACCAGAGA[C/T]CAGTCTTAGAGAGAC | 90293 |
rs180969673 | snp | A/C | 0.0374181 | 0.131563 | intron-variant | KLHL13 | GRCh38.p7 | X:117953481 | ATGGGTGCAGTGCAC[A/C]AGCATGGCACATGTA | 90293 |
rs180973365 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118006717 | GAAAGTATTTCTGTT[A/C]TAAAAACAAAAAAAA | 90293 |
rs180985467 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118032792 | ACGGTCAAATTACTC[C/T]GAGCTAAGGGAGGAA | 90293 |
rs181105165 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117944603 | AAATCCATCTGGGGA[A/G]ATTTCTTTTAAATAT | 90293 |
rs181108516 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117926089 | TTCAATTATATCCTA[C/T]AAATTTATGTTTCCA | 90293 |
rs181127192 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117960070 | ATTTTCAATCTAAAC[A/C]TTTTAAATTTAAAAT | 90293 |
rs181134586 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904510 | TGGAAAAATCTAGAG[C/T]AGGTGGCAGCAAACC | 90293 |
rs181137338 | snp | A/C/T | 0.126889 | 0.217586 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975271 | TTTCAAACAAATTTT[A/C/T]AAAACCCGAAGCATT | 90293 |
rs181137490 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991341 | AGAGAGATACTAACA[A/G]TTAAAGGTGAATGCC | 90293 |
rs181139104 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118026335 | TGTATTTTGAAAAAA[A/T]CTATGCATGGATTTC | 90293 |
rs181146731 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118110548 | CACGCCCAGCTCATT[C/T]TTGTATTTTTAGTAG | 90293 |
rs181147213 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118103246 | AAGGTATGCATAGAT[C/T]TTTTATTCTAGTGAC | 90293 |
rs181150219 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118007474 | TAGTATTTTCAATAA[C/T]GTGCCAGGGAAAAAG | 90293 |
rs181151017 | snp | A/C | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118090183 | CTAAAACCATAAAAA[A/C]CCCTAGAAGAAAACC | 90293 |
rs181153732 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118020370 | CTTTGCTGAAGTTGC[G/T]TATCAGCTTAAGGAG | 90293 |
rs181160260 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118057684 | AAAAAAAATTAGTCG[A/G]GTGTGGTGGCGGACA | 90293 |
rs181160426 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096061 | AAAGCTAGCAGAAGG[C/T]AAGAAATAACAAAGA | 90293 |
rs181164018 | snp | C/T | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118081391 | GGGTTTTGGAACAAC[C/T]TGTCAATATCTATAA | 90293 |
rs181164724 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072741 | AGCTATGCAATAGAT[C/T]CACAAAAGTTTAGAA | 90293 |
rs181165783 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117933001 | ATATCTGTTGGCCAT[C/T]TGTATGTCTTATTTT | 90293 |
rs181174434 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118063933 | AAATTATTATAGTTA[C/T]TTTAGCAATTACACC | 90293 |
rs181178194 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117917203 | AGGGAAGAGATTTCT[A/G]CTCTAAAACCATACA | 90293 |
rs181184923 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117912470 | TTAATTCCTTCACCT[C/T]TTCCCTCTTCAAATT | 90293 |
rs181187364 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:117952249 | CTCAGAAATAATGCC[A/G]CATATCTACAACTAT | 90293 |
rs181197017 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982649 | ATCACATGAGGTGAT[A/T]ATTTAAAATGTAGAT | 90293 |
rs181198675 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047654 | GGAAACAAATAAATG[C/T]TATTTTAATTGAGGC | 90293 |
rs181214553 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013915 | GGACATTTGTGACTT[A/C]CTCAATCAATACTCT | 90293 |
rs181225143 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998751 | AAACTGTCTCTGGGG[A/G]CACCATGAGAAGCTA | 90293 |
rs181242227 | snp | A/G | 0.113499 | 0.209446 | intron-variant | KLHL13 | GRCh38.p7 | X:118032898 | GAGAAGTGCTTAAAG[A/G]AGCTGATGGAGCTGA | 90293 |
rs181319363 | snp | A/C | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:117947754 | TTTCTGCTTTGGTAA[A/C]AGTACATGCCATGTT | 90293 |
rs181325531 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117963272 | CTGGGAAAAATATTT[C/T]AGTATAATTGAAAAC | 90293 |
rs181330189 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117923240 | CTGGAGTTGTTGGTT[C/T]GAAGGATATTTATTT | 90293 |
rs181331822 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117908394 | GCTATCCCTCCCCTA[A/G]CCCCCCAACCCCAGA | 90293 |
rs181350963 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117979524 | GGCCCGTTGGAAAGC[A/G]CTCAATAAGTATTTG | 90293 |
rs181356328 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994360 | CTGGGCTCAAGTGAT[A/C]CTCCCACCTTAGTCT | 90293 |
rs181362168 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118010989 | GAGGTGGGAGAATCA[A/C]CTGAGCCTGGGAAGT | 90293 |
rs181381690 | snp | C/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118094025 | GAACAAAGCTGGACA[C/G]AGAATGACTTTGACG | 90293 |
rs181389861 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118077886 | TGCAATAATTCAAAA[C/T]GAGATGGCATATATA | 90293 |
rs181395124 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118061612 | ACTCTATGCACTACA[C/T]ACTAGAGCATTTCTA | 90293 |
rs181420254 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117913995 | TATAACCAAACAACA[C/G]TCATAGTCATCCTAA | 90293 |
rs181429186 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085615 | CTGAGATTCCAGTGT[C/G]CATGATATCACTCTG | 90293 |
rs181443809 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052664 | AACCCCGTCTCTACT[A/G]AAAAAAAAACAAAAT | 90293 |
rs181455352 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939713 | GAGCTTTTTTTTCAT[A/G]TATTTGTTGGACACA | 90293 |
rs181456249 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117971701 | GCATCTGAAAGGGTT[G/T]CAAAGAAAGAGATAG | 90293 |
rs181486793 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118026468 | CTATCAAAGCAACAT[C/G]AATTCTGCTAAAACT | 90293 |
rs181541898 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118116360 | GAGAAAAAGAGGGGG[C/T]GGCGGGCAAAATGAA | 90293 |
rs181549298 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118099667 | AAAAATTTTAAAAAA[A/T]ATTAGCTGGGCATGG | 90293 |
rs181556463 | snp | A/G | 0.000168632 | 0.00918083 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117898926 | AGGTGCAGAAAGAGG[A/G]GACTCTCTAGAAGGT | 90293 |
rs181568578 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118044081 | AATCAGTAGCATTTC[C/T]ATATGTCAAAAGTGA | 90293 |
rs181588596 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956201 | TAAAGAAGGATTCAT[C/T]TGGGCAAAATATTTA | 90293 |
rs181589770 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117907941 | AATACATTAAACTAT[C/G]TTTTATTTCTTAGAA | 90293 |
rs181602123 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921479 | AATGATACAAAAAAT[A/G]AACATTTTGGCAAGA | 90293 |
rs181607012 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118022557 | AGGTGATATCTCATC[A/G]TGGTTTTCATTTACA | 90293 |
rs181609353 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118014147 | GACTGCCTACAGGGT[G/T]GGGCAGAACAGAGCC | 90293 |
rs181612920 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118036361 | CTACAAGGCTACAGT[A/C]ACCAAAACAGCATGG | 90293 |
rs181613745 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117938798 | TATCTGTTTGACCCC[A/T]TATTCTCTCTTCCCA | 90293 |
rs181615389 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077500 | TAAGGAAAGATGTTA[C/G]GTATTATGCACCAGT | 90293 |
rs181621611 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117969741 | TTTCCTGAATCTTTC[A/G]TATTTAAGATATCCC | 90293 |
rs181623609 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040028 | TTGCAAGAGCCACAG[C/T]GTTACGAGGTTTGAG | 90293 |
rs181625212 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955114 | ATATTCAAACATCTG[A/T]GTTACCCAATTTTAG | 90293 |
rs181625450 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118060618 | CTCATTTTACAGATT[A/T]AAAAAAACAGAGGCT | 90293 |
rs181627966 | snp | A/G | 0.00370173 | 0.0428621 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986497 | AACAATCTGTTGAAT[A/G]AGTAGATCAATCAAA | 90293 |
rs181631520 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118043926 | AGAAATAAAGGCTTA[A/C]AAAATGGAAAGGAAG | 90293 |
rs181723625 | snp | A/C | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117899992 | AGAGTTTTCTGTGGG[A/C]AGAGTGAGGGTGGAT | 90293 |
rs181728093 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118068457 | CGGAAGGAAATACTA[G/T]GACTCCATCACCCCA | 90293 |
rs181732829 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093404 | TGAGGAAACCATGAC[A/G]CAATAAAATGAAGTA | 90293 |
rs181745546 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930326 | AGGCAGGCAGGAAGG[A/C]AGGAAGGCAGGAAGG | 90293 |
rs181755692 | snp | C/G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117963547 | GTGCATGTGTCTTTA[C/G/T]AGCAGCATGATTTAT | 90293 |
rs181778190 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118115873 | AGGCTATTTAGTGAA[A/G]GAATGATCTCATCAC | 90293 |
rs181781356 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099550 | CACAGTGGCTCACAC[C/T]TATAATCTCAGCACT | 90293 |
rs181784183 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118085970 | TGAGACGGAGTTTTG[C/T]TTTGCTGCCCAGGCT | 90293 |
rs181788299 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117995204 | TTTTCTTTAAAACTT[A/G]CATTTATCTTTAAAG | 90293 |
rs181794163 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118067813 | TTCTGGAATACCTTC[C/T]GAAGGACCTGCCTGA | 90293 |
rs181799459 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052931 | AAACTTAGAGCCCAT[A/T]AAGAAAATAATGTTT | 90293 |
rs181867046 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986689 | GAAATCTCTTCCAAA[C/T]TCCACTTTCCTGAAC | 90293 |
rs181867079 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117970703 | GTGATCTAAAATGGT[C/T]AAAAACTAAACAACA | 90293 |
rs181877946 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118002108 | ACCTGCATCTATAAA[A/C]AAGACAATAATTATT | 90293 |
rs181879974 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118017613 | CTGACCCTCCCAAGA[A/C]CCGGTGTATATATGT | 90293 |
rs181888833 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030477 | ACTAATTGCATCTAG[A/G]ATGAAACATACAGGT | 90293 |
rs181927143 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086057 | ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 90293 |
rs181933804 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118105246 | ATTTCTCTAGAATCT[A/G]TTTTCTAACATGCCT | 90293 |
rs181934184 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117915195 | TCTGTTAATCTTTAC[A/G]GGTAAATACAATTTA | 90293 |
rs181954673 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118106452 | TTTCTAAAAAATATA[C/T]AAATTTGAATACTGC | 90293 |
rs181968662 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078859 | TTTTCCAGGGTAGCT[A/G]TACCATTTTGTACTT | 90293 |
rs181977399 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096303 | ATACTATAAACACCT[A/C]TACACAAATAAACTA | 90293 |
rs181989667 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118082665 | TGAAGCTTAGCCAAA[A/C]ATTTCTTTCCCCAAA | 90293 |
rs181993382 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118064856 | CTCAAAGGGTGGCTA[C/T]AAGGTCTGAATGAAA | 90293 |
rs181995789 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922603 | CAATAATAAAATGAG[C/T]TGTGCTTAAAGTGTT | 90293 |
rs182000482 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050039 | AATATCATTCCTCCC[A/G]TCTTTTCTTTCTTTC | 90293 |
rs182006378 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117955592 | ATTTTTAAGACAGGG[A/G]AGAATAATACAAAAA | 90293 |
rs182023693 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948130 | CTGCTAAACATCCTA[C/T]AAAACAGGACAGTTC | 90293 |
rs182029163 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117904691 | CAAATAAAGCTTTAT[C/T]GGAGCACAGCCTCAC | 90293 |
rs182039918 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117980522 | GTTAGAAGATCACCT[A/G]GTTATCCAATCTCTT | 90293 |
rs182040120 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117980252 | TTTTCAGTAATAAGC[A/G]TATCACATACCAAAT | 90293 |
rs182048952 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117918559 | AAAAACAAGCTCCAA[A/G]ACCTCTGGAAGTCTT | 90293 |
rs182049545 | snp | C/G | 0.118143 | 0.2124 | intron-variant | KLHL13 | GRCh38.p7 | X:118011665 | TCCAGGATGATGCCC[C/G]AGTTTCTGAGTCAGA | 90293 |
rs182057708 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117953379 | TGGACACAAGAAGGG[A/G]AACATCACACTCTGG | 90293 |
rs182058608 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118011307 | TCTGTGCAGGAGAAA[A/G]GCCTGGTGAGGTAGA | 90293 |
rs182062737 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117934578 | CAGAACAAGAAGGGA[A/C]CATAAAGCTGAAGGT | 90293 |
rs182063654 | snp | G/T | 0.266271 | 0.24947 | intron-variant | KLHL13 | GRCh38.p7 | X:117966441 | aagaacattccatgc[G/T]catgggtaggaagaa | 90293 |
rs182073862 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118036435 | GCCCTCAGAAACAAC[A/G]CCGCATATCTACAAC | 90293 |
rs182083783 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117983156 | CTGTGTCCCTGGTTA[C/G]CTTTCTGACCTCCAG | 90293 |
rs182096419 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117964763 | CCATAACAGTCCCCA[A/G]AGTGTGATGTTCGCC | 90293 |
rs182099864 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951179 | CAAAGGAACATGTTT[C/T]GAAAAAATCGGGAAC | 90293 |
rs182102597 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117980836 | TTACACTTCAAAAAA[C/G]GCTCAATTTCAAACT | 90293 |
rs182114850 | snp | A/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117996255 | TTGTGTGATAGTTGT[A/T]TTCTTTGCAGTTGGT | 90293 |
rs182119017 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118012081 | TGAGACCTGGCAATG[C/T]TGTTGCTTTTTAAAG | 90293 |
rs182130839 | snp | G/T | 0.118143 | 0.2124 | intron-variant | KLHL13 | GRCh38.p7 | X:118024087 | TGTTATAAACTAGGG[G/T]CCATAAGACTAGGTC | 90293 |
rs182136837 | snp | A/C | 0.249687 | 0.25 | intron-variant | KLHL13 | GRCh38.p7 | X:118036754 | aaatgggatctaatt[A/C]aactaaagaacttct | 90293 |
rs182231341 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118111840 | GAGGTTGCAGTGAGC[C/T]GGGATCATGCCACTG | 90293 |
rs182239243 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094250 | TGACGAATGCACAAG[A/C]CTCAGTAGCCGATGC | 90293 |
rs182247723 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117911440 | TTATGGGATATACAT[C/G]CAGAACGTGCAGGTT | 90293 |
rs182255057 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117943580 | TTTCATTAAGTTGAT[A/C]TTCAATCTCTGATAT | 90293 |
rs182263714 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089640 | AGAAAGAAAGAAAGA[A/C]AGAAAGAAAGAAAGA | 90293 |
rs182277984 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118103454 | TAGAAACAACCCAAG[C/T]AGATAATAGGCATTT | 90293 |
rs182278276 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908206 | TCTTTCTTCCTTTCT[A/G]TCTTTCTGTCTTTTT | 90293 |
rs182278609 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117939444 | ATTTATAAATCCTTT[A/G]GGTATATGCCCAGTA | 90293 |
rs182288018 | snp | A/C | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118091317 | ACAGCAAGATGACAG[A/C]GATGTTAGAATTATC | 90293 |
rs182296277 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073112 | AAAAAAAAAACCCCA[C/T]AAATGAAGAAAGAAG | 90293 |
rs182301807 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118058398 | TCCTATTATGCTCTA[C/T]TTTATTTCATTCTAC | 90293 |
rs182302427 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016275 | ATTCCCAGCCCTGTA[C/T]TCCCTTGACATTCTA | 90293 |
rs182302965 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118057314 | AGAATGAGGTATACA[C/G]CATATACATATACAT | 90293 |
rs182310806 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029029 | TCAGTTATCAAAAAA[A/C]CATAGTATATATAGG | 90293 |
rs182318385 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118042575 | AAACTGTACAAACAC[A/C]TGAAAATTAAAATAT | 90293 |
rs182329352 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117995486 | GTGCAGAATGTGCAG[A/G]TTTGTTACATAAGTA | 90293 |
rs182340068 | snp | C/T | 0.126889 | 0.217586 | intron-variant | KLHL13 | GRCh38.p7 | X:117927026 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 90293 |
rs182347842 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913380 | TATAATAGAATACAC[A/G]TTGAAAATATAAAAT | 90293 |
rs182356687 | snp | C/T | 2.30439e-05 | 0.00339432 | missense | KLHL13 | GRCh38.p7 | X:117945523 | ATGAGAGGCCCATTT[C/T]GCTGCCTCCAAGGGA | 90293 |
rs182359203 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118022785 | TCCCAATATGTAGGC[A/T]GCCTTTTCGTTTTGT | 90293 |
rs182367372 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117961479 | ATGTCCACATCTTAA[A/C]CCCAGGAATCTGTGG | 90293 |
rs182375569 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972989 | TTCCAATCTGTAAAA[C/T]AGGGCTGTAAGGTAC | 90293 |
rs182388591 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118111894 | GAGAGAGCGAGACTC[C/T]GTCTAAAAAAAAGAA | 90293 |
rs182390920 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074961 | TAAACTACTGGTTCA[G/T]CCCCTTTGGATTGGA | 90293 |
rs182399320 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118059345 | TCCTAAGCATTTAAG[A/G]AATCTGAAGTTTTAA | 90293 |
rs182401578 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118096482 | CAGATGGATTCACAG[A/C]CAAATTCTACCAGAG | 90293 |
rs182411236 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004515 | ATAAGGAAGGATGAT[G/T]GAGACTTGTGAAAAA | 90293 |
rs182438478 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:118032050 | GGCTTAAAAAACAGC[A/G]CACCAGGAGATTATA | 90293 |
rs182459304 | snp | A/T | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:117906120 | CTTAATCAGTTACAA[A/T]GGGAATGTTAATTTA | 90293 |
rs182462716 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117919313 | ACAGGCGTGAGCCAC[A/G]ATGCCCGGCCAACAC | 90293 |
rs182540934 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118096778 | GCTGGTTCAATATAC[A/G]CAAATCAATAAACGT | 90293 |
rs182547523 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:117925209 | ATATAATGCTATTGT[A/G]AAAAAAAGCTACATT | 90293 |
rs182558807 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118071144 | GCCACATTCTCTTAA[C/T]CCAGTCTATCATTGT | 90293 |
rs182612647 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118108486 | AAATTAAACCATCAC[A/G]TTGTAACAGGCATTC | 90293 |
rs182613618 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117905148 | CAAATCCTTTGGGGG[G/T]TATAGAGGCATTTAA | 90293 |
rs182620164 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118095547 | CAAGCGGACCTAACA[A/G]ACATCTACAGAACTC | 90293 |
rs182621953 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079310 | AATCATGAAACAGAA[C/T]GAAAAAAAGGTAACC | 90293 |
rs182622850 | snp | G/T | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:117946161 | CTTTATCTTCTGTTA[G/T]TAGTAGTAGTTCTAA | 90293 |
rs182631518 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961748 | TGTCCTTTAACTTAT[A/G]GCCAACAAGATGATA | 90293 |
rs182645592 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117989021 | TATCATGTTAGTTTG[A/G]AAACATAGAAATAAG | 90293 |
rs182654204 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117992478 | AATAAATCTTTAGAA[C/G]ACACCCTGTTTATAG | 90293 |
rs182656729 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117978616 | GCAAAAATACAGAGA[A/G]ACTGAGCAGAGAACA | 90293 |
rs182668178 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118040873 | CAGCAGGCTTTTCAG[G/T]GGAAACCTTATAGGC | 90293 |
rs182668348 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118008694 | TTGTCCTCAGGGAGT[C/T]TGCATTCCAGGGAAG | 90293 |
rs182668794 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117991800 | AATTAGGCAAAGCTC[C/T]TGGCCAAAGCTTTCC | 90293 |
rs182670575 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018905 | TAGCTTTTATAGATA[C/T]ACAAGCCTAACCTTT | 90293 |
rs182673661 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118021245 | GCATTATCTCCTTTT[C/T]TTTTATTATTATACT | 90293 |
rs182678693 | snp | C/T | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:118021047 | CCTAATGCTAGATGA[C/T]GAGTTAGTGGGTGCA | 90293 |
rs182679299 | snp | A/G | 0.0240739 | 0.107039 | intron-variant | KLHL13 | GRCh38.p7 | X:118033301 | ATTGTCACATTCACC[A/G]AAGTTGAAATGAAGG | 90293 |
rs182718451 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117936582 | AGTGGCCTCATCCAT[C/G]TGCCCAATCTTATCC | 90293 |
rs182723243 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117967917 | ACTGTAAATTCACTA[A/G]GGGACAGTGTGAATC | 90293 |
rs182728473 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953954 | AAATCCTAGAAAATA[A/T]CTCAGATGAAATTTG | 90293 |
rs182728541 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007957 | TTAATCTGAAACAAA[C/G]CAATGGTACAAAGAA | 90293 |
rs182732453 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117985150 | AATTGATTTTTGTAT[A/G]TCGCTTCACAGCCAC | 90293 |
rs182740584 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118020649 | ATTACTGGGTATATA[C/G]CCAAAGGATTATAGA | 90293 |
rs182747453 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118000866 | CTGCTGGGGCTGTTA[C/T]GTAATATAGGATATA | 90293 |
rs182796492 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104592 | ATACTGCCTTGAAAG[A/T]CTGTCACCGATCAAA | 90293 |
rs182800392 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118112181 | ACGTGAAAAGTAAAA[A/C]AGTATTAAATGATCT | 90293 |
rs182800550 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118054187 | TTTTTTTCCTCATCT[C/G]CATGCTAACAAGCTA | 90293 |
rs182817667 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084048 | AATGTGGGTTGTTGT[A/C]GTGGCTCATGCCTAT | 90293 |
rs182837520 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050613 | CTCTCTCTGATTTAC[C/T]TTTTCCTTATTCACC | 90293 |
rs182842182 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118051263 | ATAAAATTTATGGCC[A/G]GGTACGGTGGCTCAC | 90293 |
rs182868921 | snp | G/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118094419 | CTACGTCTGATTGGT[G/T]TACCTGAAAGTGACA | 90293 |
rs182876686 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118079115 | TAAAAATTCAAAGGA[A/G]AAAAAGAATTCATAA | 90293 |
rs182879435 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117919218 | TAGTAGAGACGGGCT[A/T]TCTCCATGTTGGTCA | 90293 |
rs182880003 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118062153 | TCAAAATAGGAAATA[C/T]GCTTTCTGTGATGCC | 90293 |
rs182887799 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118045571 | CACTTTGGGAGGCTG[A/T]GGCTAGTGGACCACT | 90293 |
rs182908333 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117908772 | TTTAAAACAGTCATA[C/G]ATCATAATATTCACA | 90293 |
rs182917287 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923855 | GTCCCTTTACACTAT[C/T]ATTTTTAAAAAATCC | 90293 |
rs182930365 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117940497 | AGTCAATGGTAGCTT[C/G]ATGGGGATAGCATTG | 90293 |
rs182931290 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978190 | GACTATGCCTTGGAT[C/T]TATATCAAAGGTATC | 90293 |
rs182939500 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117928236 | AAATAAACAAATTTA[C/T]AATTATAATTGGAGA | 90293 |
rs182940913 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117902376 | TAAGAAGCAAACTTT[A/T]ACATTGAGAATGAAA | 90293 |
rs182943164 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117971894 | TTCAAAAGCTTTTCT[C/T]GTACTAATATTTTCT | 90293 |
rs182944720 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117956711 | GTGTAGATGAGAAGC[A/C]GACAAAAGGGGAGAA | 90293 |
rs182947250 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117984259 | ACTACAGAAGCACTA[A/C]AGTATAGGCTGTTGA | 90293 |
rs182949506 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118008181 | CCTTTGAAAATTTTA[C/T]ATAATCTTTCTAACG | 90293 |
rs182957736 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117988321 | ATAAATAATTCAGTT[A/C]CATTCCATGTAAAAT | 90293 |
rs182963092 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014582 | ACTTACTCCCTTTTC[A/G]TACACCCCCTCCCCT | 90293 |
rs182970680 | snp | A/T | 0.108827 | 0.206325 | intron-variant | KLHL13 | GRCh38.p7 | X:118033143 | AAGTGAGGGGGGGGA[A/T]TGGAACCAAGTTGGA | 90293 |
rs182973278 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118018266 | TTCATAACAATTTTC[C/T]TCGTGATATATATTT | 90293 |
rs182989834 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118787 | GAATACTTAATCTAC[C/T]GGATAGAGCACTAGA | 90293 |
rs183088378 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118092624 | AAGAAAGAACATGGT[A/C]AGCAAAATATGTGTC | 90293 |
rs183115294 | snp | A/C | 0.00528398 | 0.051128 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117819 | GGGGCCACCTTCTTA[A/C]ACCTATTCCTTTGCC | 90293 |
rs183121515 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063211 | CTCACCACTACAGTA[A/C]AATTTGGTTGTACAT | 90293 |
rs183127160 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118086455 | AGCACAACTTTGTGA[A/G]CATACTAAAAAAAAA | 90293 |
rs183129851 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118065637 | ACATAAAAAGAAACA[A/G]AGCCAACGTAGCCTG | 90293 |
rs183151117 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118037657 | CTAGATGACGAGTTA[A/G]TGGGTGCAGTGCACC | 90293 |
rs183186130 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117935958 | ATATACTAAAAGCCA[C/T]TGATTTGCACAATAA | 90293 |
rs183201467 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913453 | TCATCTGAGTTCATC[C/T]TTTATTTCATCTGAA | 90293 |
rs183208302 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117915815 | GCTAGATGCTAAAAA[C/T]TTCAAATTGCAAACA | 90293 |
rs183213560 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118004281 | ATTTATGTGTGTATA[C/T]ACATGTATACAAATA | 90293 |
rs183220985 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967308 | ACATCATGGCAGCCA[G/T]GTCAATCTAAAATTT | 90293 |
rs183222159 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118459 | GAGCTGGTGTACACT[C/T]GAGTCACTGCTTTGT | 90293 |
rs183226803 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118031820 | ATTTCTGCATTTCCA[A/T]CTGAGGTACCGGGTT | 90293 |
rs183236227 | snp | A/T | 0.13689 | 0.222949 | intron-variant | KLHL13 | GRCh38.p7 | X:117999695 | CTTAAAGTATAATTT[A/T]AAAAATCTATTAAAA | 90293 |
rs183238872 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977054 | AGTATAGGACTCTTG[C/T]AGAATCCCTACTGTT | 90293 |
rs183246894 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118101151 | TTCATATATTAATCA[C/T]CTGATGTTTATTTCA | 90293 |
rs183248413 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118087136 | AATAATTCAAATCAT[A/G]AAATCTCAAAGTTCA | 90293 |
rs183255171 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027791 | AGAATGACTACGAAA[C/T]TTGCCCAAGGCTATA | 90293 |
rs183263776 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118054847 | TTTAACATCCTATTC[A/G]ATCAAAAGCCACAAG | 90293 |
rs183279366 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117901187 | GTACTATTATGCATA[C/T]TGGAAGCACGTTTTA | 90293 |
rs183292949 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117930419 | AGAATCTACCAAAAA[A/G]GCTGCTAGAACTGAT | 90293 |
rs183295529 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118028182 | ATTGTATTCCAGGTG[C/T]TCATAATTTATACCA | 90293 |
rs183297622 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117915631 | TACAAACATAAAGTG[A/C]TTTCTTTCTCACCTT | 90293 |
rs183301799 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117949544 | TGCTATATGAGGAAG[A/G]AAAAAGCATCTCTTA | 90293 |
rs183317401 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117964425 | ATTAAGCTATTTAAT[C/T]GCTTATGAATGAAGA | 90293 |
rs183376507 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099919 | AAAGAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAG | 90293 |
rs183381111 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101373 | GCAGGTATCATGACA[C/G]ACAATACAGATAACT | 90293 |
rs183390885 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118045853 | GAGATATCATCTCAT[C/T]TCAGTTAAAATGGCT | 90293 |
rs183398391 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118068542 | GGTAGGCAAGAGGAT[A/C]CCAGCAGCCCCCATC | 90293 |
rs183428794 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:117901715 | TCACCATGTTGGCCC[A/G]CCTGGTCTCAAACTC | 90293 |
rs183447997 | snp | A/G | 2.68478e-05 | 0.00366377 | intron-variant | KLHL13 | GRCh38.p7 | X:117919748 | ATTCAATTAAATGAA[A/G]GTGGATAATTATGGT | 90293 |
rs183452468 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117906452 | AGTTTGGTTACCTCC[A/G]TAATACAGGATGTGA | 90293 |
rs183459690 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117931498 | ATTTTTTTTTTCTCT[G/T]TTCAGTAGGTGAACG | 90293 |
rs183463919 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:118113054 | AAATAAATTCTTAAG[C/T]TGAACAATGATCTGA | 90293 |
rs183479604 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991756 | ATACACAAGAACAAT[C/T]TGGGGGAGGGAGGTG | 90293 |
rs183499556 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117931989 | TGAGCACTTTCTCTA[A/C/T]CCCAGGGCTAAGCTC | 90293 |
rs183506922 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118015109 | GGACTCATAGGAGTT[A/C]AGACACTTTCCAAAT | 90293 |
rs183507251 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:117982543 | GTTGCTGAGAGAAAA[A/G]TGGTTCTTTTCTCTA | 90293 |
rs183508765 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998348 | CTGTCTGGGTCTACT[C/T]AGGAGAGAGAAACCG | 90293 |
rs183519105 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013568 | AAGATATAAATTACG[C/T]TGGTCGAGGAAACTA | 90293 |
rs183522215 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118026221 | TATTTTAAAATACCT[C/T]GGAATTGAAAAACAC | 90293 |
rs183529832 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118038098 | TACCATAGGACACAC[C/G]AAACAGTGTCTAACA | 90293 |
rs183534891 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117964969 | ATATGTGCCACATTT[G/T]CTTAATCCGGTCTAT | 90293 |
rs183540176 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118041843 | CAACCAGAAAACAAA[C/T]AACAAAATGGCTGAA | 90293 |
rs183552982 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117996782 | ACATATACCACCAGT[A/G]GCACGCACATAATAC | 90293 |
rs183563749 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118024636 | ACATAAGAAAACCTA[C/T]TCATATCATTACACA | 90293 |
rs183582817 | snp | A/T | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118093144 | GTTGATAACAATTAC[A/T]TTGCTAATTTGTCAT | 90293 |
rs183584290 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118052710 | GGCGCACCTGTAATC[A/G]CAGCTACTCAGGAGG | 90293 |
rs183589767 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075665 | TGACATGGAATAAAA[C/G]AGGAAGGGGGAGAGG | 90293 |
rs183594937 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059616 | TCAATACCAGTAGTA[A/C]AAATAATATAGCAGA | 90293 |
rs183601880 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117924378 | CTTCCAAAATTCTCA[A/T]CTGCCTTCTATATAT | 90293 |
rs183617010 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117941251 | TGGATTACATTTTAT[C/G]GAGGATTTTTGCATC | 90293 |
rs183617309 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118087454 | TTTATCTATTTACTT[A/G]TATAAATTTATCTTA | 90293 |
rs183630863 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107540 | TCTATGAAAATAATA[A/G]TAAGTATAGTTATAT | 90293 |
rs183650865 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055504 | TGAATTCAGAATCTT[C/T]AGGACTTTTTACAAT | 90293 |
rs183695949 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930262 | AGGAAGGAAGGAAGG[A/C]AGGAAGGAAGGAAGG | 90293 |
rs183703478 | snp | G/T | 0.000529661 | 0.016265 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897650 | GTTTTGATGAATAAG[G/T]TTAGATTTTGTCAAA | 90293 |
rs183708077 | snp | A/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117913846 | GACTCCATCAAAAAA[A/T]AGAAAAAAAAAAAAA | 90293 |
rs183721405 | snp | A/G | 0.00370173 | 0.0428621 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985635 | CTTTGGAGCAAAGGT[A/G]GAGTGAGACAAATAC | 90293 |
rs183726148 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045231 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 90293 |
rs183732578 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117962572 | ATATGAGCAAGTAAA[A/G]ATAATTGCCTCAATA | 90293 |
rs183732728 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118001175 | ACAAACCAGCTTCCA[G/T]GAACTAACTGGCATC | 90293 |
rs183739561 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117979087 | AGGCATGCGCCACCA[C/G]GCCCGGCTAATTTTT | 90293 |
rs183756718 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117951602 | ACAGATGAGATTTTA[A/T]AAAATAGCTGCTATC | 90293 |
rs183765017 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117980998 | GACTATTTCCAGATC[C/T]TTTTCGTTTTCCAAT | 90293 |
rs183776367 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031308 | GTTCTCTTTGTCTTA[C/T]TGAGTTTTTCCATTA | 90293 |
rs183794372 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102312 | TCCCGGCTCATATAG[A/T]AATAATTATTTTTGC | 90293 |
rs183805364 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924174 | CAATTCAGATTGTTT[C/T]CAAACAAATTCTAAA | 90293 |
rs183807997 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117957028 | CTATAGATAAAATAT[C/T]TGGATTCTAAAAGGC | 90293 |
rs183834281 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117988513 | CCAGGAGTATTTATA[C/T]TGGAAGCAATTGCTC | 90293 |
rs183927575 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118061776 | GAGACATATGAACCA[C/T]AGGGATCTCAATAAA | 90293 |
rs183976441 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117909202 | AAATAAAACCCTAAC[G/T]ACATTTTTATCTGAT | 90293 |
rs183984078 | snp | A/C/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117940662 | GAGGTCCTTCACATC[A/C/G]CTTGTAAGTTGGATT | 90293 |
rs183998224 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994498 | CTCAAGCAATCCTCC[A/G]TCCTCGGTTTCCCAA | 90293 |
rs184001741 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118011019 | TCAAGGCTGCAGTGA[G/T]CCATGATTGCACCAC | 90293 |
rs184007865 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092088 | TGGCAAGGGATAAAA[G/T]ACTTCACACTGGGTA | 90293 |
rs184014614 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117971944 | TCCTCCACCAAAAAG[A/G]ATCATGAACAATACT | 90293 |
rs184019500 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022023 | GTGTCTGTTGGCTGC[A/G]TAAATGTCTTCTTTT | 90293 |
rs184023676 | snp | G/T | 0.11768 | 0.212112 | intron-variant | KLHL13 | GRCh38.p7 | X:118035403 | TCCACCATGATCAAA[G/T]GGGCTTCATCCCTGG | 90293 |
rs184025420 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118058966 | CACCTTAGTCCTTCA[C/T]GTACAATTCTAAATC | 90293 |
rs184068941 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070551 | GTCCATACTTGTGAT[A/G]AGACATTTTCTCCAC | 90293 |
rs184070805 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912856 | TATACTGTGAGTATA[A/C]AACAAAGGCTAAATA | 90293 |
rs184079731 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055906 | ACATTGTGCTAGAAG[A/C]TCTATCCAGGGAAAT | 90293 |
rs184092858 | snp | A/C/T | 0.000821796 | 0.0202571 | intron-variant | KLHL13 | GRCh38.p7 | X:117945401 | GGTTTTTTAAAGCTA[A/C/T]GTAAACACTACCAAA | 90293 |
rs184102375 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117907887 | AAGTATAAAAGCTGA[C/G]AACAGTTATTCTATT | 90293 |
rs184124210 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117916972 | TAGTATCTTGAGATG[A/T]TCAGTTTTTATAAGT | 90293 |
rs184134501 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117921401 | TCGATTAAGAATAAC[A/G]AATTTAAAAAGATTG | 90293 |
rs184146262 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117938095 | TGTATTAGTACTTCA[A/T]CTTTTAAAATAGCTG | 90293 |
rs184150042 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118103715 | TATTACTTTAATGAA[C/G]ACCTGGGAACAGCCT | 90293 |
rs184167439 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118074675 | TGCCCATAATTATTA[C/T]CTACATTTGAAAACT | 90293 |
rs184222963 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118032846 | tgaaaactttgaaaa[A/C]aatttagaagaatgt | 90293 |
rs184233027 | snp | A/T | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118096072 | AAGGCAAGAAATAAC[A/T]AAGATCAGAGCAGAA | 90293 |
rs184234028 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926411 | TCGAAAAACAGTCAC[A/C/T]CTCAAGGATTCCAGC | 90293 |
rs184240615 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099240 | ATGCATTTCATTTTA[C/T]ACCATCTGAAACAAA | 90293 |
rs184241314 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117960506 | TCAATATTTGCCCCC[C/T]GCACCTGCCAAACAC | 90293 |
rs184249073 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117903658 | CTCTCTCGCCACATA[A/G]GAGAAAACCTAGTGC | 90293 |
rs184266133 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118066984 | CAATAGTTTCTCATT[G/T]TAAGTACAGTCATGC | 90293 |
rs184267637 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117957771 | AGTGATTTCTTTTAT[C/G]AAACTATACACACAA | 90293 |
rs184276777 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117932880 | ACCAGAATTTGTTAT[A/G]TTTTGCCTTTTTTAT | 90293 |
rs184323097 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118043325 | CCAGAAGAAATAATG[A/C]CAATCCTACTCAAAC | 90293 |
rs184337425 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117910192 | AATAAGAGTAAATTA[C/T]GCTTTTAATGTTCAA | 90293 |
rs184370396 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117921608 | TAAGAACCAACAGCA[C/T]TGATTACTCTGTCCC | 90293 |
rs184385836 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938869 | TTTTTGAGCACCTTA[A/G]AAATCTATCCTCATA | 90293 |
rs184389219 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118115538 | GTTTTAAATCCCAGC[G/T]TCTCTTAGTCTCCAT | 90293 |
rs184393155 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117969828 | TGCTATTTCTACTAA[C/T]ATTGCCACAAATACT | 90293 |
rs184395771 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117955168 | ACAAACTCAAAACCA[A/G]TTAGAAATAACTGAG | 90293 |
rs184401310 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117907366 | AGGAACTATATATTG[A/G]AAGCTAAGTAGCCGC | 90293 |
rs184404975 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085671 | GCTCCCACTTAACAG[A/T]GAGAACATATTATAT | 90293 |
rs184411072 | snp | A/G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986524 | CAAATAATTAATCAA[A/G/T]TAACTAAGCCTAGCA | 90293 |
rs184412673 | snp | A/G | 0.198994 | 0.244742 | intron-variant | KLHL13 | GRCh38.p7 | X:118021601 | TGCATAGTATTCCAT[A/G]GTGTATATGTGCCAC | 90293 |
rs184414271 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001724 | CGAAAAATTAGCTGG[G/T]CATGGTGGCACATGC | 90293 |
rs184421569 | snp | A/G/T | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118033592 | gatcctgaaggaagc[A/G/T]ctaaacatggaaagg | 90293 |
rs184424498 | snp | A/G | 0.0338441 | 0.125605 | intron-variant | KLHL13 | GRCh38.p7 | X:118017410 | ATAATTTGAAAGCGA[A/G]AAGGCAACATGGCTA | 90293 |
rs184429015 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:117937319 | TAGCAACATAGAGTG[A/G]TATCTCTATGGTACC | 90293 |
rs184454830 | snp | G/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117968422 | TCACTTCTATCTCTA[G/T]GATTTTCCATTAATA | 90293 |
rs184462815 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118110266 | AATAAAGAATTGTAA[C/T]GCACACTCATGTCCC | 90293 |
rs184468753 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118095857 | ATGAGAACAAAGACA[C/T]AACATACCAGAATCT | 90293 |
rs184484703 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118080915 | TACACAGACAGCAAG[A/G]AATACTATGCAGCCA | 90293 |
rs184486896 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117993702 | TAGAGGCAAAAAGGA[C/G]CACAGTATATGAAAC | 90293 |
rs184491574 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118063590 | TGCTTAAAGTATGTC[A/G]TGCTATATTAGTTTG | 90293 |
rs184497341 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118047280 | TATTTATAATCATGC[A/G]GTGAAGAAGGCAAGC | 90293 |
rs184501874 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118021825 | CACACTGTCTTCCAC[A/G]ATGGTTGAACTAGTT | 90293 |
rs184518778 | snp | G/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118089540 | AGCTAAGACAGAAAG[G/T]TTCATTCATAGGGCA | 90293 |
rs184527040 | snp | C/T | 0.0126344 | 0.0784702 | intron-variant | KLHL13 | GRCh38.p7 | X:118070887 | CATTAGGTATATCCC[C/T]CAATGCTATCCCTCC | 90293 |
rs184533444 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118057022 | TCCCTGTTCCTTGGG[A/T]CTTTTTTTCAGCAAA | 90293 |
rs184565608 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118085424 | TGGGATGAGTAAAAG[G/T]AGATAGATATATATA | 90293 |
rs184566717 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117920841 | AGCAACTGTATTAAG[A/T]ACACGATAGTTCTTT | 90293 |
rs184575938 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117954411 | AGATAGGTAGACGGA[C/T]GGATGGATGGATGGA | 90293 |
rs184578982 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118052512 | GGGCGACAGAGCAAG[A/T]CTCCGTCTCAAAAAA | 90293 |
rs184608137 | snp | C/G | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:117924867 | AATGCTATTTTGATG[C/G]TGGAAAATAGCATTT | 90293 |
rs184620274 | snp | C/T | 0.0152462 | 0.0859689 | intron-variant | KLHL13 | GRCh38.p7 | X:118010668 | GTGGGTGCAGCGCAC[C/T]AGCATGGCACATGTA | 90293 |
rs184624462 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117942551 | GGATAGTTACCTCTT[C/G]TTGTTGCATTGATCC | 90293 |
rs184638360 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117958269 | CCTGATTTATAAATT[A/G]GGTACAGTAAGATAT | 90293 |
rs184642747 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118035272 | TATGATACCAAAGCC[A/G]GGCAGAGACACAACC | 90293 |
rs184651870 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117989240 | TCATTTTCATTTTCA[A/T]CCTGATCCTGAGGTA | 90293 |
rs184654973 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117916683 | TGATTCACACTTTAC[A/G]TACCACTGTTCTTCT | 90293 |
rs184655197 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117902766 | AAGCTGTTAAGAGAA[C/T]TCATCAAAAGCATGA | 90293 |
rs184657110 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118005405 | GTTGACATAGATATA[C/G]GGTGTGGTAGGCAGA | 90293 |
rs184662965 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117951831 | AATCCTTGTAATAAC[G/T]CATTTAACTTACAAA | 90293 |
rs184667591 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019217 | CCATTTCTTCCCACT[A/C]CTGCCCCTGTGTTTC | 90293 |
rs184670294 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117932256 | ATTTACTATAGTCAC[C/T]CTACTGTGTAACAGA | 90293 |
rs184670685 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965236 | CTATTTCTCCACATG[A/C]TCTCCAGCACCTGTT | 90293 |
rs184677828 | snp | C/G | 0.125973 | 0.217065 | intron-variant | KLHL13 | GRCh38.p7 | X:118032421 | ACTGCCTCTTCAAGT[C/G]GGTCCCTGACCCCTG | 90293 |
rs184683912 | snp | G/T | 0.0414859 | 0.13792 | intron-variant | KLHL13 | GRCh38.p7 | X:118098481 | CACTGTTGGTGGGAC[G/T]GTAAACTAGTTCAAC | 90293 |
rs184687212 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981629 | TTAAGTCAGAGACAC[C/T]TGAGCATTTTTATGA | 90293 |
rs184692040 | snp | A/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117997685 | ATGATTCTCCTTGGA[A/T]ATAATCCATGAATCC | 90293 |
rs184704438 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118105307 | GCCTCTGTCAGAGAT[A/G]GCATGAAAGGAAGTG | 90293 |
rs184707598 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118066673 | AATATTTTGTTCTGA[G/T]AAAGACTACCAAGAA | 90293 |
rs184715907 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118114177 | AACATCAATAAAAAT[C/T]AAACAATTTGAAAAT | 90293 |
rs184717776 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954588 | CCATACCTTCTATAC[A/G]AACAAGTGAATTCAA | 90293 |
rs184718392 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093700 | TTTTGTAACTTATTA[C/G]TACATTCAACAGCAT | 90293 |
rs184752198 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985949 | CATTCCATCTAGATC[A/G]CTTTTTAAAAATAAA | 90293 |
rs184777903 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118016904 | AGAAACCAGTTGGTT[C/G]CCAAACATTGTAAAA | 90293 |
rs184843900 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118119323 | ACTTAGTTATTGTTC[A/G]TTGCTAAAAACACAC | 90293 |
rs184849638 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064478 | TGCTATTTTAAAATA[C/T]TGATTTATCACTGTA | 90293 |
rs184854756 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088461 | TCACTTTTATTACCC[C/T]TAACGCAAACAGGAT | 90293 |
rs184860919 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117969600 | TCTATTTCTATCAAG[A/T]CAATCCCTTCAGAAA | 90293 |
rs184881304 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118001397 | AACAACAAAATTTTT[A/C]ATTGTTTTCTCCTTG | 90293 |
rs184900092 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029505 | ATCTACATTTTAGTA[A/G]TGCCGATGTATAACA | 90293 |
rs184920421 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925702 | TTTGCAGAGACTTCT[C/T]TGATCTGATCCCAAC | 90293 |
rs184930088 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117912168 | TTCCCAAGACAAGTA[A/G]GAATTATCTCGTCCC | 90293 |
rs184940019 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117944316 | ACATATCTATTGATG[A/G]CCCACAGGACAATGA | 90293 |
rs184943635 | snp | A/C | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:118032615 | TCATCAAAGACCAAA[A/C]GTAGATAAAACCACA | 90293 |
rs184948568 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975028 | ATATTTAAAAGTTTT[A/T]TTTAACCTGCCATTA | 90293 |
rs184950539 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959778 | CTCATTGATCAGTGA[A/C]AAGCTCTATATTTTT | 90293 |
rs184954875 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118101800 | CTGATGGTTTTATAA[A/G]TGTTTAGAAGTTCCT | 90293 |
rs184967827 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118048127 | CACAACTCTTACAAG[G/T]AGTGTTCCTTTAATA | 90293 |
rs184976854 | snp | A/G | 0.138243 | 0.22363 | intron-variant | KLHL13 | GRCh38.p7 | X:117913574 | AACAAGGCCGGGGGC[A/G]GTGGCTCACGCCTGT | 90293 |
rs184997885 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118097951 | GATTAAAGACTTAAA[C/T]GTTAGACCTAAAACC | 90293 |
rs185001592 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118084584 | AATTCCAACTCTCAA[C/T]TTTTATCTCACAATT | 90293 |
rs185010765 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117946899 | ATCTTGCAATAATTA[A/G]CAAAAATTCTGGCCT | 90293 |
rs185011332 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118066394 | AAATACCAACTGGAG[A/G]CAATAACTCCTAGTA | 90293 |
rs185012830 | snp | A/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117978939 | ATTTTATTTTATTTT[A/T]TTTATTTTTGAGACA | 90293 |
rs185021923 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118051734 | TGAATACACAAATTC[A/G]ATACAATTACAATCA | 90293 |
rs185040234 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118009025 | CAATCTCTCCTAACA[A/C]CACCAAAATATAAGA | 90293 |
rs185068316 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030069 | CTTCATTGTCGTCAG[C/T]CCTCTTCCAGCCCCT | 90293 |
rs185098553 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117929694 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGTTGA | 90293 |
rs185113225 | snp | A/G | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117962161 | GCTGCAGGGAGCCAT[A/G]ATCATGCCACTGTAC | 90293 |
rs185121454 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117908066 | GTCAACTACAAGGAC[A/T]TTATTTATTTATTTA | 90293 |
rs185134060 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117993091 | CATGGAGAGCCCTAA[G/T]TGGACTAGCACAGAG | 90293 |
rs185211749 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118086646 | TATCACGTACTTCCA[C/T]TTGTGTTTAAAAGAG | 90293 |
rs185215979 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069053 | ACTCTGCTGCTGAGC[A/C]AACAGCGCTTTGGTG | 90293 |
rs185216269 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117999516 | CATGGACACAGGAAG[A/G]GGAACATCACACACC | 90293 |
rs185220476 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118105942 | AGTCTCGCTCTGTCG[C/T]CCAGGCTGGAGTGCA | 90293 |
rs185226372 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094043 | AATGACTTTGACGAG[A/T]TGAGAGAAGAAGGCT | 90293 |
rs185228461 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118014427 | CTAGTCAGACCAGTT[A/C]TCTGCTCTTGAACAC | 90293 |
rs185237128 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118027332 | GCTCCTTCTGACTTC[C/T]TTTTGTTTCCTAGTC | 90293 |
rs185247845 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118040401 | TCCTATCAGACGAGA[A/G]CTGAAAAATACAAAT | 90293 |
rs185252504 | snp | G/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117910623 | ACTATCATTCATTTT[G/T]GTTCCTTCAAAGTTA | 90293 |
rs185303563 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117966159 | ATCTAGAAAACCCCA[C/T]TGTCTCAGCCCAAAA | 90293 |
rs185316049 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998810 | TGGTGAAGATGCTCA[A/G]AAAACAGCCTGCTGA | 90293 |
rs185332288 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026341 | TTGAAAAAAACTATG[C/T]ATGGATTTCAATTTT | 90293 |
rs185376780 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118109070 | ATGCTCCCGCCTAGG[C/T]GTCCCAAAGTGTTGG | 90293 |
rs185394444 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118080583 | TTACACCAGTGAGAA[C/T]GGCTGTTATTAAAAA | 90293 |
rs185399152 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117953305 | TAAACTATCGCAAGG[A/G]AAAAAACCAAACACC | 90293 |
rs185407605 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118047089 | AAGAGAAGGGGGGAT[A/G]ATTGAATAAGTGATT | 90293 |
rs185420269 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117901222 | TAGGAGAACTTATAT[A/G]TTATATAATGATACA | 90293 |
rs185432308 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982808 | TTAGCTATAGTAAGA[C/T]TGTCTTCTTTCTCAG | 90293 |
rs185442525 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118014062 | TTGAACAATATTAAA[G/T]CAGTGCACCCTAAGA | 90293 |
rs185443494 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117915677 | ATTCTATATATTTGT[A/G]TATTTAAATTGTAAT | 90293 |
rs185454292 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117950086 | CCCTCATTTGTTTCA[C/T]AGTGCTTTAACTGCC | 90293 |
rs185458404 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117930974 | ATTTTATGATCATAA[C/T]GTTGAGAAAAAAGGA | 90293 |
rs185459868 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118038496 | ATCTGTGCACTAGAG[C/G]AGAGAGATTGCAGTA | 90293 |
rs185462389 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117964512 | TCCTCAGCAGAGTTA[C/T]GCCTGGCACATAATA | 90293 |
rs185463732 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117923607 | GCAAATATTTTACAA[C/T]TGGAATTGAATAATG | 90293 |
rs185464519 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118103549 | TAAAAGTAAGAAAAA[A/T]TGTAAGAAGAAAAAG | 90293 |
rs185469059 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908525 | ATATATGTCACAACA[C/T]AAAATGTGGACTTCC | 90293 |
rs185470453 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118091372 | CATAAAAATGCTTCA[C/T]TGAGCAATTATGAAA | 90293 |
rs185473159 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111988 | GAGGCAAGTTCTATT[A/G]CCCCTTTTTTACATA | 90293 |
rs185475231 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117956309 | CTGATGATTTGGGGA[A/G]GGGCTATTCCAAATT | 90293 |
rs185476767 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117980630 | TCACAGAAAGCTAAT[C/T]CTAATGACTAATTAA | 90293 |
rs185477240 | snp | C/T | 0.0199298 | 0.0978146 | intron-variant | KLHL13 | GRCh38.p7 | X:117939966 | TCCCATTTGTCAGTT[C/T]TGGCTTTTGTTGCCA | 90293 |
rs185478664 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118017731 | AACCATGTATTAACA[C/T]TCACTGCTATATCCC | 90293 |
rs185479033 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117995766 | ATCTAATCATTTGTG[C/T]TTGGCTCCTTTCACT | 90293 |
rs185480722 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073654 | TAGAAAGTCATAGAA[A/G]AGTTAAGGAATAATT | 90293 |
rs185481563 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117979896 | CAGCAACTTCCTAAG[C/T]ATCTCCTTAAACTAC | 90293 |
rs185484647 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030632 | TGTTTAGCCATGGGG[C/G]CACCACCCTCATGAA | 90293 |
rs185501124 | snp | C/T | 0.0850455 | 0.187856 | intron-variant | KLHL13 | GRCh38.p7 | X:118095585 | CAAATCAACAGAATA[C/T]ACATTCTTTTCAGCA | 90293 |
rs185514564 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060855 | AAACAACAGATTCAA[C/T]ATGTCAGCACAGTTG | 90293 |
rs185521237 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118063401 | ATGAGAAAAACATTA[C/G]AGGTACTGAAATGAA | 90293 |
rs185522666 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118043950 | AAGGAAGAAATCAAA[C/T]TATCCTTGACTGCAG | 90293 |
rs185524486 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117925348 | TAAGTAGAGAAAAAA[C/T]GAAACACATCCTGAA | 90293 |
rs185536397 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959260 | CACGCACCCTCTGTA[A/G]GAAAGTGATCGTAAC | 90293 |
rs185554345 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118012713 | GGGTATTCTGTCTAC[C/T]GCTGGTAGTATTTGT | 90293 |
rs185558519 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117990019 | AGGAGGCGATTTTGG[C/T]GAAATCAAGCCAGCA | 90293 |
rs185568190 | snp | A/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118037860 | AGTCAAGAACTGAGA[A/T]AAGAGCCCAGACAAT | 90293 |
rs185626458 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093351 | ACATACACTACTTTA[C/T]CTAATTTCTATAAAA | 90293 |
rs185640028 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060049 | GAATATAAATATGAA[C/T]GAGGAACAGTACCTA | 90293 |
rs185641066 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911880 | ATTGCTTATTTTACT[C/T]AGTAGCTACATATTT | 90293 |
rs185671739 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117943835 | TACTTCTGTCAGTTT[G/T]TCAAACTCATTCTCT | 90293 |
rs185687617 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117973994 | AAAATTGAAGCTGCT[C/G]TCAAAGGCAGCTTGA | 90293 |
rs185692032 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118025592 | ACTGGTGACTTGGAT[A/G]TATCAAAGAGAAGCC | 90293 |
rs185694001 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118006292 | AGTCTAACAGAATGT[A/T]TTTTACCAAAGAAGG | 90293 |
rs185739391 | snp | G/T | 0.0465453 | 0.14528 | intron-variant | KLHL13 | GRCh38.p7 | X:118091177 | AGATATACCTAATGT[G/T]AAATGACGAGTTAAT | 90293 |
rs185745857 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118105008 | CAGTAAAAAGATTGT[C/T]AATTTGTTTTAACCT | 90293 |
rs185752803 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118072774 | GTTTTCTCTTCCTGA[C/T]GAATTGAAGCCTATA | 90293 |
rs185758713 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118057813 | TCTGGGCAACAGAGC[A/G]AGAGTCCATTTCAAA | 90293 |
rs185761393 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111873 | CTCCAGCCTGAACGA[C/T]AGAGTGAGAGAGCGA | 90293 |
rs185761957 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076549 | GACTTGTGGAGCATC[C/T]TGTAGAGAAAAAAAG | 90293 |
rs185763638 | snp | G/T | 0.0510748 | 0.151422 | intron-variant | KLHL13 | GRCh38.p7 | X:118096386 | TAAACCAGGAAGAAG[G/T]TGAATCTCTGAATAG | 90293 |
rs185771604 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118082983 | TATGCCAGTACCGTG[C/T]TGTTTTCCTTACTCA | 90293 |
rs185773930 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971915 | AATATTTTCTTTAAA[A/C]AAAGATTCGGTTTTC | 90293 |
rs185778527 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117988420 | GCAGGATGACTTAAG[A/T]GGTTTACAGAATTTT | 90293 |
rs185782225 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065304 | TAATTAAAATTCATT[C/T]TAAAAGGTAAATGTA | 90293 |
rs185782522 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118003685 | TGTGGATGTTGACTA[C/T]AGGAAAGCAGAATTT | 90293 |
rs185782634 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118043687 | TGATAAAATTCAACA[A/T]CGCTTCATGATAAAA | 90293 |
rs185789527 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118036415 | AGATCAATGAACAGA[A/T]CAGAGCCCTCAGAAA | 90293 |
rs185793553 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118050338 | ATTGAAAGTATTATC[C/T]TTGTATTAATGCAAT | 90293 |
rs185795564 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018446 | TTTACTAGTCCTTTA[C/T]TTAGTAAATTAATGA | 90293 |
rs185803788 | snp | C/T | 0.112567 | 0.208835 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031532 | ATATATATTTAGTTA[C/T]ATATATATTAGTTAT | 90293 |
rs185805751 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117919260 | AACTCCCAACCTTAG[A/G]CGATCTGCCCGCCTC | 90293 |
rs185839470 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118100281 | AAAATAGCATGGGCC[A/G]ATGCTGCAGCTGCTA | 90293 |
rs185839755 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117953512 | TACATATGTAACTAA[C/T]CTGCACATTGTGCAC | 90293 |
rs185843534 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118007005 | ATCAAATAATTATCG[C/T]TCCCTAGAGGCCTTA | 90293 |
rs185851820 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117983756 | ATAAGATCCTATTTG[C/T]TTTTAGAAGCTTTCT | 90293 |
rs185870365 | snp | A/T | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118078246 | GGGTTTAATTTTAAA[A/T]TTTTTAATTAGGTTT | 90293 |
rs185890493 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044301 | GCTAAAATGTCCATA[C/T]TACCCAATGCTATTT | 90293 |
rs185924089 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117900856 | AGAGGTGGTCATTAC[A/G]TTAAAGTGAGACTTC | 90293 |
rs185950479 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905410 | CTACTCTAAGCCTCC[C/G]CTAGTTTCCCATTGT | 90293 |
rs185952395 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117935453 | GGTTGCTGTATTAAT[C/T]CATTCTCACACTGCT | 90293 |
rs185959528 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117915488 | ACTGATAACAAATGT[C/G]CAGGTGAAACCAGTA | 90293 |
rs185966903 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117923 | TATTGTGATTTTTTT[C/T]CTTTGGCTGTTTTTT | 90293 |
rs185970860 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117990748 | CAAGAGGGCCCAATG[C/T]GAACAAGCCCTTTTA | 90293 |
rs185978861 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967178 | TGACAAAGGGCTAAT[A/T]TCCAGAACTGAGCAT | 90293 |
rs185980704 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118020019 | AAGTAGTTTTTTCCA[A/T]TTCTGTGAAGAAAGT | 90293 |
rs186002695 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117960132 | TCTGTAATCCCAGCA[C/T]TTTGCGGGGCACAGG | 90293 |
rs186010114 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118061683 | TTACTGCAAAAGCAA[C/T]GGAACCTCTGCAAAA | 90293 |
rs186019892 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991453 | TTTCTAATTCAAAAT[A/T]TAGAATTCATTTTGC | 90293 |
rs186021857 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975637 | CTCAGGTGATCCACC[C/T]GACTTGGCCTCCCAA | 90293 |
rs186036250 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118007575 | TCTGCTGCTTCTGTT[A/G]TTTGTTTCCCCTAAA | 90293 |
rs186042530 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020387 | ATCAGCTTAAGGAGA[C/T]TTTGGGCTGAGACAA | 90293 |
rs186064996 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118048904 | AAAACTGACAAAACT[C/G]CTTATGATAGTTGAG | 90293 |
rs186068073 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117939647 | CTAACTGGCATGAGA[C/T]GGTATCTCCTTGTGG | 90293 |
rs186072121 | snp | C/T | 0.0605624 | 0.163136 | intron-variant | KLHL13 | GRCh38.p7 | X:117908350 | CTGCACCCATCAACC[C/T]GTCACCTACATTAGG | 90293 |
rs186100180 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117970868 | ATAGAGTGTTGTAAT[A/G]TCAAAATAGTCTGTT | 90293 |
rs186115281 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118111671 | GCCGAGGCAGGTGGA[C/T]CACGAGGTCAGAAGA | 90293 |
rs186131491 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118058574 | CAGTTATGCAACGTG[C/G]CCAAATGAATGCTGG | 90293 |
rs186135980 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118082292 | ATGTCTTTTTGATAA[C/T]AGCAATTCTAACAGG | 90293 |
rs186146121 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023317 | GTTGTTTCAGAGAGA[G/T]AATTTTTTCATATTA | 90293 |
rs186156661 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027894 | CAATCAAGCTACTGG[C/G]AATAAGACAGACTCT | 90293 |
rs186175641 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117904609 | TTTACATTTTTTACA[A/C]ATTGAAAAAGAATCA | 90293 |
rs186201657 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117917410 | GGATGTCTGCAAAGG[A/G]TGCAAAAAAAAAAAA | 90293 |
rs186207388 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117922786 | TGCTTGTATGTTTTT[C/T]GAAGTCAAAATACAG | 90293 |
rs186211799 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955627 | AGACAGGCTCTCAAC[A/C]TAATGAGTCTGAGAA | 90293 |
rs186228128 | snp | C/T | 0.00475684 | 0.0485365 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986755 | TTGCTTCTGTGATAT[C/T]TTACATGGTAATTTG | 90293 |
rs186264218 | snp | A/G | 0.0194105 | 0.0965841 | intron-variant | KLHL13 | GRCh38.p7 | X:118096245 | AAAATGACAAAGGGG[A/G]TATCACCACCGATCC | 90293 |
rs186271604 | snp | A/T | 0.0199298 | 0.0978146 | intron-variant | KLHL13 | GRCh38.p7 | X:118011776 | GGATTGGACATTGGA[A/T]ATGTCATGTTTACAA | 90293 |
rs186284316 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118116149 | AGAGACAGTAGGGCC[C/G]GGGCGGGCAGCGGGA | 90293 |
rs186284766 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077713 | CATAACTTGGCCTGT[C/T]CTACTATCTGAGACT | 90293 |
rs186285441 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118064795 | TGCTAGCTGTTTTCT[A/G]TGTGTTTTAATTTCT | 90293 |
rs186310248 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118099610 | AGGCCAGGAGTTCGA[A/G]ACCAACCAGCCTGGG | 90293 |
rs186310281 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118085974 | ACGGAGTTTTGCTTT[A/G]CTGCCCAGGCTGGAG | 90293 |
rs186311668 | snp | A/G | 0.0110639 | 0.0735497 | intron-variant | KLHL13 | GRCh38.p7 | X:118041462 | AGGCCAGGAGGTCTC[A/G]AGGCTACAGTGAGCT | 90293 |
rs186326444 | snp | C/T | 0.00166926 | 0.0288417 | intron-variant | KLHL13 | GRCh38.p7 | X:117899428 | TAGTTTTGAAGTAAA[C/T]AATTATAGAAATGCA | 90293 |
rs186327101 | snp | C/T | 0.0157677 | 0.0873799 | intron-variant | KLHL13 | GRCh38.p7 | X:118068178 | ACATGACTATAATAT[C/T]GCATTCTTATTTACA | 90293 |
rs186331620 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930294 | AGGAAGGAAGGAAGG[A/C]AGGCAGGCAGGCAGG | 90293 |
rs186336840 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118033135 | GTACCTGAAAGTGAG[A/G]GGGGGGAATGGAACC | 90293 |
rs186341189 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118053191 | AAGACGCATGCACAC[A/G]TATATTTATTGCAGC | 90293 |
rs186374051 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117987549 | AATACCCAGTAAGTA[C/G]GCAAGCTTTCGTTGA | 90293 |
rs186392850 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118017957 | CAATCAGAAAATACC[A/G]CCACAACAACAAACT | 90293 |
rs186410782 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117904940 | GTTATCTCACATATA[C/T]CAGGAGTTCTTATTT | 90293 |
rs186424661 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117918690 | ATTAAGTACTCCATC[A/G]ATTGGTAGTTGTATG | 90293 |
rs186432400 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117953442 | TAGCATTAGGAGATA[A/C]ACCTAATGCTAAATG | 90293 |
rs186434059 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117934658 | TAGAATACATATATA[A/T]GTAAAATATATATAT | 90293 |
rs186440621 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117966498 | CCCAACATAATTTAT[A/G]GATTCAATGCCATCC | 90293 |
rs186449716 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117983238 | TCTCACAGTGTTGTC[A/G]TGAAAACCAAAGTAA | 90293 |
rs186458444 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998847 | ACACAGGGAACCATG[A/T]AGCAAAACCATATAA | 90293 |
rs186465634 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014279 | GGAAGAAATGCATTC[A/C]TGAGGGTAGGTCTAT | 90293 |
rs186502159 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913997 | TAACCAAACAACAGT[C/G]ATAGTCATCCTAAAG | 90293 |
rs186531634 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108843 | ACAGGGTCTCACTCC[A/G]TCACCCAGACTGAAG | 90293 |
rs186545698 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947814 | CTATCTCCCCTTTAT[G/T]AAGTTTATTGATTGA | 90293 |
rs186570085 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971839 | CATTTTTCCTACTGA[A/T]AAATATTTTAAAAAT | 90293 |
rs186595019 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118103299 | TTATCCTACCTACTA[C/G]CTGTGAGATCACCAC | 90293 |
rs186600902 | snp | A/T | 0.0312828 | 0.12109 | intron-variant | KLHL13 | GRCh38.p7 | X:118002643 | AAATAAATAAATAAA[A/T]AAAATGCTGTGGGAT | 90293 |
rs186613898 | snp | C/T | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030860 | ATAAATTTCTGCTCA[C/T]TGTAAATCAATCTGT | 90293 |
rs186618134 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016307 | ACCATGAAGACATGA[G/T]TATACATTACGTCAG | 90293 |
rs186623212 | snp | A/C/G | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029049 | GTATATATAGGGTTC[A/C/G]GTACTCTCCACGTTT | 90293 |
rs186629275 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118042712 | AAATGATAATGTAAA[A/C]AAAACATACAAAACC | 90293 |
rs186634578 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117980325 | TTCTATATTATTTCA[A/G]AAATACCTATACTTT | 90293 |
rs186651690 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118011436 | GGCTGCAAAGAGAGA[C/G]AGAAACTGTCAGGGG | 90293 |
rs186670558 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117927992 | TGTTAATTTACAAAA[A/G]TAAAAGTAAAAGGAT | 90293 |
rs186671036 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102615 | GGTAGTCACTAATTT[C/G]TGTTGAATTAATTTG | 90293 |
rs186676543 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913390 | TACACATTGAAAATA[C/T]AAAATATGAAGTTTA | 90293 |
rs186680577 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118071245 | TCTTTATAGCGGCAT[C/G]ATTTATAGTCCTTTG | 90293 |
rs186704534 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117961501 | AATCTGTGGATATGT[C/T]GTTACATGGCAAAGG | 90293 |
rs186704634 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118054196 | TCATCTCCATGCTAA[A/C]AAGCTATAATTCAAT | 90293 |
rs186708877 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117978305 | TCACACCATGATGGC[A/G]TAAGCAATGTGAAGG | 90293 |
rs186719472 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117992058 | TGGCATGAATGAGTT[G/T]AGTCAAGTTTCTTCA | 90293 |
rs186757626 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104910 | GAGTGAATTATATCT[C/T]AATAAAGCCGTTAAA | 90293 |
rs186821870 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | KLHL13 | GRCh38.p7 | X:117965344 | TGATGGCCAGTGATG[A/G]TGAGCATTTTTTCAT | 90293 |
rs186831403 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930330 | AGGCAGGAAGGCAGG[A/C]AGGCAGGAAGGCAGG | 90293 |
rs186852219 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117963831 | CAGTGATGATGAGCA[C/T]TACATATACACCATG | 90293 |
rs186865661 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117995335 | CAACCTAACATCATC[C/T]TATTCCCCATAAAAT | 90293 |
rs186873140 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117933359 | CAGAAATAAATCCAT[C/G]TATTTACAGCCAAGT | 90293 |
rs186876463 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118022605 | TGTTGAGCACCTTTT[A/T]ATATGCCTGTTGGCC | 90293 |
rs186888184 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118089816 | GGGTGTGGTGGCTCA[C/T]ACCTGTTATCCCAGC | 90293 |
rs186896179 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912773 | ATTTTTGTAGGCACA[C/T]AGTTGGTATATATAT | 90293 |
rs186902841 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118057539 | AAAAATGTGAAAAAT[C/T]GGCCGGGGCCGTGGC | 90293 |
rs186904467 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944798 | AAGCTTCTAATCCCC[A/G]TGCTAAATAGCTCCA | 90293 |
rs186949160 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118051266 | AAATTTATGGCCGGG[C/T]ACGGTGGCTCACACC | 90293 |
rs186949743 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086325 | AGACCTACTTTTAGT[C/T]CTTTGAGAAATCTCT | 90293 |
rs186972333 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118053955 | GGGTCCTAGTTACCA[G/T]GGAAAATCCTATTTC | 90293 |
rs186987824 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117992492 | ACACACCCTGTTTAT[A/T]GGTTATGATCTACTT | 90293 |
rs186987886 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008985 | ATGACTCTTGCCAAT[A/G]CAACTACTATGAGTA | 90293 |
rs186995920 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118021247 | ATTATCTCCTTTTTT[A/T]TTATTATTATACTTT | 90293 |
rs187003845 | snp | A/G | 0.0157677 | 0.0873799 | intron-variant | KLHL13 | GRCh38.p7 | X:118033396 | AACAGCAGATCTCTC[A/G]GCAGAAACTCTACAA | 90293 |
rs187008001 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104596 | TGCCTTGAAAGACTG[C/T]CACCGATCAAAATTA | 90293 |
rs187021716 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118092720 | AATATTTCTGTATCA[A/T]CATTGTGGAGGTGGT | 90293 |
rs187026513 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075246 | GCTGTGTGTGGAAGA[A/C]GATGAGAATTAGCAA | 90293 |
rs187033238 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118059451 | TCAATCATCTTAACC[C/T]TGCTATCAACGTATA | 90293 |
rs187112554 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926185 | AAAAGTTTAAAAACA[G/T]TGAAGGAAAGGGATC | 90293 |
rs187137827 | snp | A/T | 0.104598 | 0.203367 | intron-variant | KLHL13 | GRCh38.p7 | X:118099669 | AAATTTTAAAAAAAA[A/T]TAGCTGGGCATGGTG | 90293 |
rs187156795 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118068495 | TGTGAGATAACCTGG[A/G]AACCAGAAGGAACTT | 90293 |
rs187177774 | snp | A/G | 0.125973 | 0.217065 | intron-variant | KLHL13 | GRCh38.p7 | X:118036440 | CAGAAACAACGCCGC[A/G]TATCTACAACTATCT | 90293 |
rs187185247 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:117926967 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 90293 |
rs187194835 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117960931 | TGATTTTATTCAAAA[G/T]GTAGCACTATTACTA | 90293 |
rs187198303 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117924403 | ATATATCTACTTTTT[C/G]CTTTCACTCATAAAT | 90293 |
rs187200555 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118094261 | CAAGCCTCAGTAGCC[G/T]ATGCGATCAAATGGA | 90293 |
rs187204339 | snp | G/T | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:117910457 | CAGATGGAAACTTGG[G/T]AAAATAGAAGGTTGT | 90293 |
rs187211058 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941744 | TCTTCATTAATCTGG[A/C]TAGCGGTCTATCTAT | 90293 |
rs187217623 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117991758 | ACACAAGAACAATTT[G/T]GGGGAGGGAGGTGGA | 90293 |
rs187222071 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117980936 | TATTTGCCCACTATG[C/T]CACTATCCAAGAGAC | 90293 |
rs187224910 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117996575 | AAGAATGCAGCAATA[A/C]ATTCTTGGGCATGCC | 90293 |
rs187226456 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973080 | TAGTGCCAGAAAAGC[A/G]TTGACTGCAGTATAT | 90293 |
rs187230678 | snp | A/C | 0.0157677 | 0.0873799 | intron-variant | KLHL13 | GRCh38.p7 | X:117957938 | AGATTTTTAAAAAAA[A/C]CTTATTTTCCTTATC | 90293 |
rs187230761 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012216 | ATATTAGGAAGCCTT[C/T]GTGCCAGACTCTGAA | 90293 |
rs187230845 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118061783 | ATGAACCATAGGGAT[C/T]TCAATAAAAATTACT | 90293 |
rs187233913 | snp | A/T | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:118040168 | CCACACTGCAAAGAT[A/T]AAAATAAATACATAA | 90293 |
rs187237133 | snp | A/G | 0.0245906 | 0.108123 | intron-variant | KLHL13 | GRCh38.p7 | X:118020798 | ACATATACACCATGG[A/G]ATACTATGCAGCCAT | 90293 |
rs187238442 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118024277 | CTGGTTTGCGGTCAA[G/T]AATGCATTTATAATG | 90293 |
rs187270721 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117940609 | TTGTTTGTGTCCTCT[C/T]TTATTTCCTTGAGCA | 90293 |
rs187278377 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117932031 | TATTTCTTATTAAAA[C/T]TTAATTTTTAATTAT | 90293 |
rs187280741 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117902402 | TGAAAATATACACAC[C/T]TCTTGGTTTATGTTC | 90293 |
rs187285026 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117916219 | CACAGTATTTAACAT[A/G]TTGTAGTTATACAAT | 90293 |
rs187285234 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117956775 | AAGGTGTTAAAAGTT[G/T]CCCTAGCTAGTCGGA | 90293 |
rs187401914 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118098150 | AACAGGCAACCTACA[A/G]AATGGGAGAAAATTT | 90293 |
rs187402770 | snp | C/T | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118085362 | AAAGCAGAATCATAA[C/T]TGCCAGGAACTGGGG | 90293 |
rs187412669 | snp | A/C/G | 0.000328315 | 0.0128082 | intron-variant | KLHL13 | GRCh38.p7 | X:117945402 | GTTTTTTAAAGCTAC[A/C/G]TAAACACTACCAAAG | 90293 |
rs187415616 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118107405 | AAAAATAGCATTCCA[A/G]CTAGGATTAAGACAA | 90293 |
rs187416979 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118052279 | GCACTTTGGGAGGCT[A/G]AGGCGGGCGGATCAC | 90293 |
rs187419204 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977908 | TACATGCATGTGTGT[G/T]TGTGTGTATCTCTTA | 90293 |
rs187431637 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078906 | AGAGTTTTACTTGCT[C/T]ACAATCCTTGCCAGC | 90293 |
rs187432703 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118026515 | TCAAATTTATCACAA[A/T]GTTTGGGTGGAAGAA | 90293 |
rs187455499 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118008056 | AAACTTTGTCCTTTG[A/G]CTATATATTTTTAGA | 90293 |
rs187457451 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118045282 | GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 90293 |
rs187489926 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118107591 | GCTTAGCACTCTATA[C/T]GCATTATTAATTTAA | 90293 |
rs187492732 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118094535 | GATTCAGGAAATACA[A/G]AGAACGTCACAAAGA | 90293 |
rs187492817 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117906294 | TATTCTGCAAAAACA[A/G]TGGGTCCAAGAAAAC | 90293 |
rs187492946 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117919383 | CCTGTTTCAATCTCA[C/T]CTTGCTTACAGACCA | 90293 |
rs187499417 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118079917 | AAAATAGCATAGTAC[C/T]GGTACAAAAACAGAC | 90293 |
rs187507048 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117953807 | ACATTCTGTTATAGG[C/T]AAGTAATTTTCTGGT | 90293 |
rs187508462 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079128 | GAGAAAAAGAATTCA[C/T]AAAATTCAAAAGAAA | 90293 |
rs187511427 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936111 | TGACAACCTGGAATA[A/G]TAGGGAGAAGTGAAA | 90293 |
rs187515703 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118046633 | TCCAATTACATGTCT[G/T]TATCTAAACAGCTCA | 90293 |
rs187516910 | snp | C/T | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:118062333 | TCAAGTATTTCCTTC[C/T]TTCTCTTATTATATA | 90293 |
rs187521287 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118045731 | AGAATTGCTTGAACC[C/T]GGGAGGCAGAGATTG | 90293 |
rs187527949 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117921285 | TATTTTTAATTTTTG[C/T]GGGTACAGAGATGTA | 90293 |
rs187531100 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117954412 | GATAGGTAGACGGAT[A/G]GATGGATGGATGGAT | 90293 |
rs187540228 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118008568 | GACACATTCCTCTAC[A/G]TTCACTTCCTGCACT | 90293 |
rs187541024 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117981770 | CAGATTTGTAAAGCA[C/T]AGAACAACATAACAT | 90293 |
rs187543432 | snp | A/C | 0.00738971 | 0.0603345 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985804 | TAGTTGCCAGTCATT[A/C]AGTCCTATCTTTTTT | 90293 |
rs187545839 | snp | C/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118018849 | TCCAACTATTTTTTA[C/T]AACTCATTAGTTCTA | 90293 |
rs187550241 | snp | A/G | 0.0419931 | 0.138684 | intron-variant | KLHL13 | GRCh38.p7 | X:118031862 | GGAGTGCCAGTCAGT[A/G]GGTGCAGGCCAGTGG | 90293 |
rs187550676 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117997971 | AAAGCACTTTCATGT[C/T]CTTGATTTCATTAAT | 90293 |
rs187553313 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013278 | GGCCACTTTAGATTG[G/T]ATGGTCAAAGGAAAC | 90293 |
rs187555728 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118033159 | TGGAACCAAGTTGGA[A/G]AACACTCTGCAGGAT | 90293 |
rs187681464 | snp | C/G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117978653 | CAGTTGTTGGGGACC[C/G/T]GATGATCCACAGATT | 90293 |
rs187712731 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118112806 | TCAAGGAAGGGCTTA[G/T]GGCAATAAATTCATT | 90293 |
rs187717991 | snp | A/G | 2.4365e-05 | 0.00349026 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909353 | CAGATATCCTTTGAG[A/G]GCACTTAGGTGGAAG | 90293 |
rs187723941 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118084208 | TGGTCACATGCACCT[A/G]TAGTCCTACCTGCTC | 90293 |
rs187747557 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118095558 | AACAGACATCTACAG[A/G]ACTCTCCACCCCAAA | 90293 |
rs187753744 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907564 | TACTTGCACCTTCTA[A/G]ATATTTCCAGATACC | 90293 |
rs187755715 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941176 | TGAATTTTGTCAAAG[A/G]CCTTTTCTGCATCTA | 90293 |
rs187757498 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118063256 | ATGTGCTGTACTTTA[A/G]AGGAGTGGAAAAAGG | 90293 |
rs187769780 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117972100 | CTTAAAATACATTTT[A/T]AAAACAGACATTTGT | 90293 |
rs187770492 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117937423 | ACTTTCACATCACTG[G/T]TCTTTCTCAGCCTGG | 90293 |
rs187770945 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117919809 | ATAAAATCAAAGGAA[A/C]GTCTTATCTTATATA | 90293 |
rs187778355 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004297 | ACATGTATACAAATA[C/T]TTCCTAGCTCTCTCC | 90293 |
rs187789553 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936628 | GACTCCTACCCTCAC[A/T]GTTCTGCTCTGTCTA | 90293 |
rs187796403 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:117967933 | GGGACAGTGTGAATC[C/T]TATAATTAAAAAAAA | 90293 |
rs187800007 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117968678 | TATCAATTTAATAAG[C/T]ATTTTGCTAGAAAAG | 90293 |
rs187800726 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117954012 | ATTTAAAAGAACACA[C/T]TCTGAACTCTAATGC | 90293 |
rs187806660 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118021169 | CAGTATTTTTTGTTC[A/G]ATATCTGCCTTATTT | 90293 |
rs187817157 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001248 | CAAACTCAAAAGATG[A/C]CCTTTGGAAACTTTT | 90293 |
rs187818489 | snp | G/T | 0.00370173 | 0.0428621 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985614 | GAACAGGAACAAAGT[G/T]TTCATCTTTGGAGCA | 90293 |
rs187818843 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000996 | CATCGTAAATTTAAT[C/T]TCATTAAATTAAGGA | 90293 |
rs187828195 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016094 | ATATGAAGTTAATCA[C/T]ATATGTGTTTCTTTA | 90293 |
rs187838643 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118028224 | TAAATATATTCTCTA[C/T]TTTTTCATTATCTCA | 90293 |
rs187885502 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118646 | GATCTGCATTTGAAC[C/T]GCCAGTAGCTTGCAC | 90293 |
rs187896253 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101213 | AATTACCCAGTCCTA[A/G]CTACTGGAAAATACT | 90293 |
rs187904559 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118063469 | TGGGCTTCATTTCCC[C/T]TACACTGGGCCAATA | 90293 |
rs187910355 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118047096 | GGGGGGATGATTGAA[C/T]AAGTGATTTCAGGAC | 90293 |
rs187912317 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118087221 | CTCTAAACTCTCATC[C/T]CTGTTAAGAAGTTAA | 90293 |
rs187918322 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118069626 | ATATGTATATATGTA[C/T]GGATATAAAAAAAGA | 90293 |
rs187993852 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118096484 | GATGGATTCACAGAC[A/G]AATTCTACCAGAGGT | 90293 |
rs187994032 | snp | C/G | 0.00175003 | 0.0295288 | intron-variant | KLHL13 | GRCh38.p7 | X:117901815 | ATATTATATTGTGTT[C/G]ACATGATACTTGTTT | 90293 |
rs187998792 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101944 | AAACTCTTTCCTTTA[G/T]AAATTATCCAGTCTT | 90293 |
rs188001957 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117931554 | CATTCTGTGTAATTC[C/T]GCTGTTTCTATCAAG | 90293 |
rs188003169 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088809 | TGGCTAACAATCATG[G/T]ATATTGTATATAAAA | 90293 |
rs188016966 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065738 | CCTCCCTAGGCTCCA[A/T]TAGGCTAGAGCAAGC | 90293 |
rs188017721 | snp | C/T | 0.0131573 | 0.0800346 | intron-variant | KLHL13 | GRCh38.p7 | X:118070638 | TATGTATAACCATAA[C/T]AGATTTTTTTTTGTC | 90293 |
rs188024262 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117924257 | CTCCTTCTGACTATA[C/T]ACATTGTTGTGTACA | 90293 |
rs188025344 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056053 | CAGAGCAGATGACAT[A/G]AGCTTGTACGTAGAA | 90293 |
rs188028467 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117957081 | TGACCACCTTTGACC[C/T]TTGCTTCTTCCCCAT | 90293 |
rs188053875 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117989136 | CAGATACTCCACAAA[A/G]TATTTTACTTGCTTT | 90293 |
rs188056302 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117988765 | ATCAGGACCCTCTTA[C/T]ACATTTCTAAAATGG | 90293 |
rs188066471 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118018907 | GCTTTTATAGATATA[A/C]AAGCCTAACCTTTTT | 90293 |
rs188074699 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913910 | CCTGTGGGAACCTAT[A/C]AAATTGTTCTTAAAA | 90293 |
rs188076697 | snp | A/G | 0.00427583 | 0.0460395 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898899 | AGCATCTTAGTTGTA[A/G]AGATGATCTTAAGGT | 90293 |
rs188085585 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947753 | ATTTCTGCTTTGGTA[A/T]CAGTACATGCCATGT | 90293 |
rs188089586 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930274 | AGGAAGGAAGGAAGG[A/C]AGGAAGGAAGGAAGG | 90293 |
rs188103741 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962752 | TGAAAGTAGCAAAAG[C/T]CTATAAAAATGAAAA | 90293 |
rs188112221 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117979134 | ATGGGTTTTTACCAC[A/G]TTGGCCAGGCTGGTC | 90293 |
rs188113926 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994122 | CCACCAACTCCCATC[G/T]TTCCATCAACCACGA | 90293 |
rs188239564 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924032 | TATTTTCACAACATA[C/T]AGTGTCCCTTTCTAA | 90293 |
rs188247028 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104164 | GAGGTCAAGGCTACA[A/G]TAAGCTGTGATCATG | 90293 |
rs188261046 | snp | C/T | 0.105069 | 0.203703 | intron-variant | KLHL13 | GRCh38.p7 | X:118085834 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTATCATAT | 90293 |
rs188263982 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074693 | ACATTTGAAAACTGG[A/G]CCTCCAGTAAAGTCA | 90293 |
rs188265132 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118067355 | CTGAGTGAGTCAGTA[A/G]GTGAGTGGTAAGTGA | 90293 |
rs188271309 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093148 | ATAACAATTACATTG[A/C]TAATTTGTCATTTAC | 90293 |
rs188274888 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052805 | GCACGCCAGTCAGGC[C/T]GACAGAGCAAGACGC | 90293 |
rs188279717 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117951639 | AGGCTATAAGAAGCT[A/G]TTGCACAGGCTATAA | 90293 |
rs188288784 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030734 | GTTCTCTCTCTCCCT[C/T]TGCCTCTTTTTGCCC | 90293 |
rs188292737 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118083907 | AAAATAGATGCACTA[C/T]GCATCTAGTTTAATA | 90293 |
rs188294898 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951353 | AATTATAAATATCAT[A/C]GCAACTTCTCTCTCT | 90293 |
rs188296223 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117981204 | ATGTACAACATCATT[A/T]GCACATGCCACATCA | 90293 |
rs188305403 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050808 | AAATGAAAATATGAG[C/G]AAGACAGCATAAAAT | 90293 |
rs188315967 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012624 | AAGTCCACTTTGCCA[C/T]GAACAGTGTCATAGT | 90293 |
rs188320373 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117916793 | AAATAGTGTTTTGAT[C/T]ATGTGAACTATAATA | 90293 |
rs188328107 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911881 | TTGCTTATTTTACTT[A/G]GTAGCTACATATTTT | 90293 |
rs188328327 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117951934 | GAAGAACATTCCATG[C/T]TCATGGGTAGGAAGA | 90293 |
rs188332417 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117932644 | TTTAGTTTAATTCCA[C/T]GTCTTAGCTATTGTG | 90293 |
rs188338017 | snp | C/T | 0.0240739 | 0.107039 | intron-variant | KLHL13 | GRCh38.p7 | X:118037664 | ACGAGTTAGTGGGTG[C/T]AGTGCACCAGCATGG | 90293 |
rs188341181 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004573 | ATACAAATATGAGAC[C/G]ATTTGGCATCAAAAT | 90293 |
rs188355851 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118032139 | AGTCTGAGATCAAAC[A/T]ACAAGGCGGCAGCGA | 90293 |
rs188389349 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994666 | CACATTCAGCTTCTT[C/T]CTTGAATTATTTATA | 90293 |
rs188395638 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118011301 | GCATGCTCTGTGCAG[A/G]AGAAAAGCCTGGTGA | 90293 |
rs188405795 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118022528 | TTCTGATAATGGCCA[A/G]CCTAATAGGTGCAAG | 90293 |
rs188415991 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036349 | CTTCAAACTATACTA[C/G]AAGGCTACAGTCACC | 90293 |
rs188482487 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117969694 | AATAAAGACTATTTG[A/G]TCATCAATCAATCTA | 90293 |
rs188499910 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118897 | GAGCAAAATAATACT[G/T]GTCTGATATGCCCCA | 90293 |
rs188513930 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118087999 | CACTTTTAGGATAAA[C/T]TTTATTTATGACCAT | 90293 |
rs188515792 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908914 | TTCTGTAATGAAGGA[C/T]TGTAACCTGTTCAGT | 90293 |
rs188528508 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055607 | AAATTTAAGGGGTTG[C/T]AAAAAAAATTCAGTA | 90293 |
rs188530744 | snp | C/T | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:117913567 | AAAGAACAACAAGGC[C/T]GGGGGCGGTGGCTCA | 90293 |
rs188548638 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967730 | TGTTATATTAAATGA[C/T]TTCAAGAGGTCTTTT | 90293 |
rs188548777 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092112 | CTGGGTACAGTGTAC[A/G]CTGCTTGAGTGATGG | 90293 |
rs188559877 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117946391 | GTAAGAATAGGAGAA[A/C]CTTAGTCAGTAGGTC | 90293 |
rs188560736 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118059157 | GTTCTACAAGTCTCA[A/G]CAGATCCTACAGCAT | 90293 |
rs188584160 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965011 | ATTTGGGTTGGTTTC[A/G]AGTCTTTGCTATTGT | 90293 |
rs188596643 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117997648 | CATTTAATAAATTGC[A/G]GGTAAGGTCCTTCAA | 90293 |
rs188606259 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025928 | TGTTTATATTTGTGA[A/G]TAGAAGAGATGAGCA | 90293 |
rs188612887 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118024847 | CAGTAGCTTACTCTA[A/T]GTCCCAGCAGTTCCA | 90293 |
rs188623859 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117944385 | ACTGGGGAAATGGGA[A/T]TTTACTGAATTCAAA | 90293 |
rs188631592 | snp | A/G | 0.112567 | 0.208835 | intron-variant | KLHL13 | GRCh38.p7 | X:118105933 | TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 90293 |
rs188633628 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998600 | GACATTATTGGAGAG[C/G]GCACAGCCACAGCAC | 90293 |
rs188637635 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975183 | AGAAATACATACACA[C/T]ACACACACACACACA | 90293 |
rs188642011 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117959945 | TACAGAGGGATCGCA[C/T]AAGCACAAATTAAGC | 90293 |
rs188644679 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118093734 | CTTCCTGAAATATTA[C/T]GACAAAGTCTTATAA | 90293 |
rs188648068 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013768 | CCCGAACGGAGAGAC[C/T]GGCTGGAGCCGAGGC | 90293 |
rs188648405 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077725 | TGTTCTACTATCTGA[A/G]ACTGATTTTTACCTC | 90293 |
rs188652766 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117990924 | GAGGAGAAATATCAA[G/T]AATATTTACATAATG | 90293 |
rs188654953 | snp | C/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118026242 | TGAAAAACACAAATA[C/T]TACATTTTCAAAATA | 90293 |
rs188657362 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118061531 | CAATAATTTAGGACA[A/G]AGTCTTTACGGAGGC | 90293 |
rs188662802 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038208 | AGTGAAGTGATGAGA[G/T]TGGGAAATGTTACTC | 90293 |
rs188665458 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044007 | CCTAAAGGCTCCACC[C/G]AAAAACTATTAGAAC | 90293 |
rs188755591 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118099661 | TCTAATAAAAATTTT[A/T]AAAAAAATTAGCTGG | 90293 |
rs188766740 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118095740 | GGATTAAGAAACTCA[C/T]TCAAAACCGCTCAAC | 90293 |
rs188774037 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118086040 | CTTCCCGGGTTCAAG[A/C]AATTCTCCTGCCTCA | 90293 |
rs188774775 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117906706 | GTTTAGTACAGAATG[C/T]GTTTGATGGGTATGC | 90293 |
rs188788942 | snp | C/T | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118101400 | AACTGAGTTAGCCCC[C/T]GTCCTCAAGGAATTC | 90293 |
rs188799258 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070070 | GTCACATGCATTACA[C/G]GTTTGTAGCCTGTGA | 90293 |
rs188827383 | snp | G/T | 0.121377 | 0.214374 | intron-variant | KLHL13 | GRCh38.p7 | X:117928679 | ATCAAAAATTGTGGA[G/T]TGCAGATGAAGCTCT | 90293 |
rs188833472 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961871 | GACATTTTTATTTTA[A/G]CCCCGTGAGACCAGT | 90293 |
rs188837474 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117984909 | AACTGAGTGAAATTA[C/T]GTATTTCTACATAAG | 90293 |
rs188853769 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118014796 | GGGGCTGATTCCCCC[A/G]ATACCCCCAAAATGG | 90293 |
rs188866898 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041881 | CAACATTGAATCTAC[A/G]TGACTAAATCCTACA | 90293 |
rs188872805 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021766 | CCAGTAATAGGATGG[C/T]TGGGTCAAATGGCAT | 90293 |
rs188895791 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118038034 | ATGTAGAGAATAAGG[A/G]AAAATATTGAAAAAA | 90293 |
rs188982301 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904674 | TTCAAATTTCATGTT[C/T]ACAAATAAAGCTTTA | 90293 |
rs188995634 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118110993 | GTCCTCTATTTACAG[C/T]TATTGCATGAGTAAA | 90293 |
rs189001048 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958861 | TTTTTTCTCTAATCC[A/C]TAAGGGTATCAGTTC | 90293 |
rs189006960 | snp | C/T | 0.0220041 | 0.102557 | intron-variant | KLHL13 | GRCh38.p7 | X:117918174 | AACAATATAGCACCA[C/T]GCTGCCATAAAAACC | 90293 |
rs189010491 | snp | A/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117953374 | AAACATGGACACAAG[A/T]AGGGGAACATCACAC | 90293 |
rs189016525 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117989246 | TCATTTTCAACCTGA[C/T]CCTGAGGTAGGCAAT | 90293 |
rs189016814 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118081499 | CATATTTTTGGGGTG[C/T]ACATAATATTTTTGA | 90293 |
rs189020657 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117933854 | GATAAAATGTATGAA[C/T]AGAAGAAGCTACTAA | 90293 |
rs189030258 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048488 | TTTTTTGTTGAGGAT[A/C]TAAAACAAAAATGGC | 90293 |
rs189031335 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109301 | ACATTTATGTCCATT[A/C]ACTTTCCCACAGGTC | 90293 |
rs189032947 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118005558 | GGATTATTCAGTTGT[A/G]CTCCTCAACATTGGA | 90293 |
rs189041632 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118019313 | AAGTGTCTGTTCATA[A/T]CCTTCGCCCACTTTT | 90293 |
rs189045645 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:117912906 | AAAAAGTAAAGATAC[A/G]ATGATAGATGCAATT | 90293 |
rs189049135 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118032471 | GGGAGGCACCCCCCA[A/G]CAGGGGCAGCCTGAC | 90293 |
rs189051673 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080770 | ACTGGGTACATACCC[A/C]AAGGAAATTAGATCA | 90293 |
rs189088298 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055124 | CAGGTCTGAATAAAG[A/G]TAACAGTTTTTCTGG | 90293 |
rs189148738 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118009964 | CTTGAAGAAGACATT[C/T]ATGCAGCCAAAAAAC | 90293 |
rs189151572 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987075 | TTGGGCAGCAACTCT[A/G]AAGTACTATGCAACA | 90293 |
rs189163703 | snp | C/T | 0.150751 | 0.229455 | intron-variant | KLHL13 | GRCh38.p7 | X:118033614 | ATGGAAAGGAACAAC[C/T]GGTACCAGCTGCTGC | 90293 |
rs189169380 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118017740 | TTAACATTCACTGCT[A/G]TATCCCTAGCACCCT | 90293 |
rs189176753 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118095997 | ATCTAAAATTGAAAC[C/T]CTAACATCACAATTA | 90293 |
rs189191216 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118081209 | TAACAAACCTGCATA[C/T]GTGTACACCCTGTAT | 90293 |
rs189195258 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063712 | TAGCAGCAATGTGAA[C/T]TCTGGAGCATCTAGC | 90293 |
rs189205970 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047486 | GAAAACAATAACATA[C/T]AATGGTAAAATAAGG | 90293 |
rs189228795 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907913 | CTATTCTCTGATAAA[C/T]AGCTTAGTCTCAAAT | 90293 |
rs189249601 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117921466 | TATGCAATTTAACAA[C/T]GATACAAAAAATGAA | 90293 |
rs189260332 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955077 | AAAGAACTGTGTTTC[A/G]CCTTCCTAAGATTTT | 90293 |
rs189267437 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118115831 | ACCTAGAAAGAAACT[C/T]TAAAGTTCCCTAGTT | 90293 |
rs189268582 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117938096 | GTATTAGTACTTCAT[C/G]TTTTAAAATAGCTGG | 90293 |
rs189283837 | snp | C/T | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118096098 | CAGAACTGAAGGAAA[C/T]ACAGACACAAAAAAC | 90293 |
rs189289408 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118102371 | CCAGCTTAGGTATCA[A/C]CATAGGATTAAGTTC | 90293 |
rs189295481 | snp | A/C | 0.0353775 | 0.128208 | intron-variant | KLHL13 | GRCh38.p7 | X:118089636 | AGAAAGAAAGAAAGA[A/C]AGAAAGAAAGAAAGA | 90293 |
rs189308073 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064541 | CTAACATTAGGTAAC[C/T]GACATGACTCTCTTT | 90293 |
rs189312618 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118059959 | AGCATCTAGCACTTA[A/G]CATTACTCATAAATG | 90293 |
rs189347154 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040221 | CGAAAATCTACAAAC[A/G]TTGAGACCACCCAGG | 90293 |
rs189349943 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913679 | TGAAACCCATCTCTA[C/T]TAAAAATACAAAAAT | 90293 |
rs189365921 | snp | A/G | 0.0168099 | 0.0901243 | intron-variant | KLHL13 | GRCh38.p7 | X:117930209 | GGGCAAGAAAGGATG[A/G]AAAGGAAGAAGGAAG | 90293 |
rs189391984 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947897 | ACCCCAAGCCACAAT[A/T]ATATCAATCTATGCT | 90293 |
rs189398082 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979959 | GCTTTTCTGATTGAA[C/T]CTGTGAACTTATCAA | 90293 |
rs189400428 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001522 | AATGAACATGAGTAT[A/G]CAAGGCTAAATCCTG | 90293 |
rs189414188 | snp | A/C | 0.00949095 | 0.0682305 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029991 | ATAATAATAAAAGAA[A/C]AGAAAAAGAAAAAAG | 90293 |
rs189437949 | snp | A/G | 0.0245906 | 0.108123 | intron-variant | KLHL13 | GRCh38.p7 | X:118021942 | TCTAACTGGCGTGAG[A/G]TGGTATCTCATTGTG | 90293 |
rs189439978 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118002547 | ACGGTGAGCTGAGAT[C/T]GCACCATTGCACTCC | 90293 |
rs189550648 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118098942 | GGGTGGGGGAAGGGG[A/G]GTGGGGGAAGGGGGG | 90293 |
rs189551770 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117955572 | TTTTCAATATGACAG[C/G]CAGTATTTTTAAGAC | 90293 |
rs189553501 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099518 | ACACAGCTATTAAAT[A/G]AATGCACTCGGCTGG | 90293 |
rs189558049 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117970552 | CTAATTCAGTCTTTA[C/T]CATTTTTGAAGTGGA | 90293 |
rs189560267 | snp | G/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986544 | TAAGCCTAGCACTAA[G/T]AACTCAGTACATACC | 90293 |
rs189565529 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118066754 | TGATGAAAGATTTAC[A/T]TCCAGAATCAATAAA | 90293 |
rs189566338 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118001798 | TGAGCCTGGGAGGCA[A/G]AGGTTGCAGTGATTG | 90293 |
rs189577286 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118017460 | GAACTCTAATTAGAA[A/C]CTAGAGAAAAATGAA | 90293 |
rs189584262 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076220 | GGAGCATAAGAAGAG[A/G]ATGTTGTAATGTGTT | 90293 |
rs189584928 | snp | A/T | 0.00528398 | 0.051128 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030091 | CCAGCCCCTGAATTT[A/T]AGGAAAAGAAATAGA | 90293 |
rs189600534 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117904171 | CTTAAGCTTTTTTCC[A/G]GCTAAAAATGCATCT | 90293 |
rs189604040 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118043456 | AAACTATAGGCCAAT[A/G]TATCTGATGAACATT | 90293 |
rs189629431 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902825 | TATTTATTGCAGACA[C/T]TGCCAACTGCTAATC | 90293 |
rs189637388 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117932974 | AATTAGTGTTGTTGT[A/G]TAATTTTCCATATAT | 90293 |
rs189650872 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117925585 | TAGGCTGGACATAAA[C/T]GTTTATATTAATTTT | 90293 |
rs189651231 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118103435 | AACTACTTTGGCCCC[C/T]GAGTAGAAACAACCC | 90293 |
rs189661617 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930322 | AGGCAGGCAGGCAGG[A/C]AGGCAGGAAGGCAGG | 90293 |
rs189662178 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117908382 | ATTTCTCCTAATGCT[A/C]TCCCTCCCCTAGCCC | 90293 |
rs189664995 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117965672 | AAAATACTGGCAAAC[C/G]GAATCCAGCAGCACA | 90293 |
rs189668128 | snp | G/T | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:118091286 | AGTATAATAAAAAAA[G/T]TATCAATAGATGTTG | 90293 |
rs189669333 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986146 | CATGTATTCTGACAA[C/T]ACAAAATATGGTGTA | 90293 |
rs189674095 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072888 | CACTTGAGCCCAGGA[A/G]TTTGAGACCAGCCTG | 90293 |
rs189683495 | snp | C/G/T | 0.00317446 | 0.0397266 | intron-variant | KLHL13 | GRCh38.p7 | X:118058299 | TTCCCCTACTCCCCC[C/G/T]CTCATTTTTATTTCT | 90293 |
rs189683769 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118017048 | GTCTCCTAATTTTCC[C/T]GTCCTCCTTCCCCAA | 90293 |
rs189718284 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118020298 | GGCTCTTTGTTTGTC[C/T]GTTGTTGGTGTATAA | 90293 |
rs189809886 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118114461 | GTCTTACTATGCAAT[C/T]ACATTAGCAGCAATC | 90293 |
rs189826714 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118105156 | GTTCCTTGCTTTTCA[A/G]TAAGACCTCCTTTAA | 90293 |
rs189827619 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118085428 | ATGAGTAAAAGGAGA[C/T]AGATATATATATATA | 90293 |
rs189836787 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117980720 | AACTTTTACCATTTC[C/T]TAGGTTTAATCATTA | 90293 |
rs189843161 | snp | A/G | 0.022522 | 0.1037 | intron-variant | KLHL13 | GRCh38.p7 | X:118076556 | GGAGCATCTTGTAGA[A/G]AAAAAAAGGTCTCAT | 90293 |
rs189849736 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118052582 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 90293 |
rs189852377 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117996060 | ATATGATAACTCTAT[G/T]TTCAACTTTTTAAGG | 90293 |
rs189862787 | snp | G/T | 0.0110639 | 0.0735497 | intron-variant | KLHL13 | GRCh38.p7 | X:118023320 | GTTTCAGAGAGATAA[G/T]TTTTTCATATTATAA | 90293 |
rs189882795 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117917147 | TGTTCCTGGAACTAA[C/T]CATCTGCCAGATTTT | 90293 |
rs189906745 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118100472 | TTATGTTAATTATCA[C/T]GGGAATTGATAGTAT | 90293 |
rs189912618 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118086973 | AAATAAGGATGTTAC[A/G]CTACAAAAAAAAACT | 90293 |
rs189917025 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:118106167 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGC | 90293 |
rs189918612 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117952031 | CTACCAATGACTTTC[C/T]TCACAGAATTGGAAA | 90293 |
rs189923250 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069130 | ACACACACACACACA[C/T]ACACACACACACACA | 90293 |
rs189926298 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923697 | TTGTGCATCATGTAT[A/C]GTCAGCTGTGTAATT | 90293 |
rs189928712 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982567 | TTCTCTATGCTGCAA[C/T]ACATATACCAAAAGA | 90293 |
rs189933132 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118054656 | GCTAAAATGACATAG[A/G]CTAATATGAATTAAG | 90293 |
rs189934478 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117908618 | TTTTGGGTTAATTTA[C/T]ATAGCCAAAGTATTC | 90293 |
rs189942074 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117940250 | AAAGATCAGATGGTT[G/T]TAGATGTGTGGCATT | 90293 |
rs189950249 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971849 | ACTGATAAATATTTT[A/T]AAAATAACACTCAAA | 90293 |
rs189953369 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982839 | TCCCTGGCCTGCCTT[A/C]GCATATGAACACTGG | 90293 |
rs189956249 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117956426 | TTCTTGGGTAGAACA[C/T]ACCATTGTGATAAAA | 90293 |
rs189959776 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007450 | CCAAATTTGGACAAA[A/G]TTATATATTAGTATT | 90293 |
rs189960246 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117987972 | GGGGACATTAAAATG[A/G]TTTAATCAACAGCAC | 90293 |
rs189970249 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014070 | TATTAAATCAGTGCA[C/T]CCTAAGAAAGAACAG | 90293 |
rs189979693 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118032876 | TATAACTAGAATAAC[C/T]AATATAGAGAAGTGC | 90293 |
rs189986796 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118039799 | ACCCAGGGCTGTGCT[A/G]GCATCAGGTGGGACC | 90293 |
rs190026328 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108050 | ACAGAATGAGACCCT[A/G]TCTTAAAAGAAAAAA | 90293 |
rs190028400 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118094592 | ACACATAATTGTCAG[A/G]TTCACCAAAGTTGAA | 90293 |
rs190041116 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079190 | AAATTCGCAGAAAAA[G/T]AAATGTGAATATCCG | 90293 |
rs190046482 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118062816 | TGAAAGCCACATATG[A/G]TGACTTACAGAGACC | 90293 |
rs190084167 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089924 | TCTCTACTAAAAATA[C/T]ACAAATATTAGCCAG | 90293 |
rs190084272 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093359 | TACTTTATCTAATTT[C/T]TATAAAATCTCTTGT | 90293 |
rs190098395 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118057544 | TGTGAAAAATCGGCC[A/G]GGGCCGTGGCTCATG | 90293 |
rs190103600 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060591 | CAACCCAGAGAAGAA[A/C]GTATTATTACCCTCA | 90293 |
rs190138994 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118012294 | GTGGCTTTAAACAAC[C/G]CTAGTTGATGATCTT | 90293 |
rs190145458 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118024479 | GTAAGCCATGGACTG[G/T]AAGGAAATATTCACA | 90293 |
rs190149853 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | KLHL13 | GRCh38.p7 | X:117911149 | TTAAATGTTTGGTTG[C/T]TTTTAAAATTTTGTC | 90293 |
rs190153400 | snp | C/T | 0.113965 | 0.209748 | intron-variant | KLHL13 | GRCh38.p7 | X:118037623 | GGGGGAGGGATAGCA[C/T]TGGGAGATACACCTA | 90293 |
rs190155346 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117943229 | TCCCTTTGTAGGTAA[A/C]CCGACCTGTCTCTCC | 90293 |
rs190169195 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117925942 | GCCACCTGTCTCAGC[C/T]TCCCAAAATGCTGGG | 90293 |
rs190175629 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117912361 | CTACCAGTTGCCAGT[C/T]ACCAAACTGAAATCT | 90293 |
rs190177155 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117914928 | CAAGGTTATAGGAGG[A/G]ATATTTAGAATATTT | 90293 |
rs190199316 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117944003 | TTGGTGACCTTCAGA[A/T]GCGGTTTCTGTGTGG | 90293 |
rs190199682 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974444 | AAATAGTTAGCGTTC[A/G]AATATTCTTTCCAAA | 90293 |
rs190202083 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117966190 | TCTCCTTCAGCAAAG[A/T]CTCCTCCTAACTTCA | 90293 |
rs190210153 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998818 | ATGCTCAAAAAACAG[C/T]CTGCTGAGCAAGCAC | 90293 |
rs190220090 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118006337 | TAAATATGTGAAATG[C/T]AGATTTCTGAGGCAA | 90293 |
rs190228839 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118026353 | ATGCATGGATTTCAA[A/T]TTTTTTGCATGAAAA | 90293 |
rs190319216 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102660 | TTTTCTCTCATTAGA[C/G]AAAGTGCTGCCCTAC | 90293 |
rs190321591 | snp | A/G | 0.0271702 | 0.113344 | intron-variant | KLHL13 | GRCh38.p7 | X:118061867 | AATGTTTCAAATTAC[A/G]AAATTCTATGTGTTA | 90293 |
rs190331800 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118045570 | GCACTTTGGGAGGCT[A/G]AGGCTAGTGGACCAC | 90293 |
rs190339807 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118068281 | GAGAGGAAGATGGCC[A/G]ACTAGAAGCCCCTAG | 90293 |
rs190342882 | snp | A/G | 0.0369084 | 0.130736 | intron-variant | KLHL13 | GRCh38.p7 | X:118071287 | AGTAATGGGATGGCT[A/G]GGTCAAATGGTATTT | 90293 |
rs190367316 | snp | A/G | 0.0394543 | 0.134798 | intron-variant | KLHL13 | GRCh38.p7 | X:118070976 | GTGTTCTCACTGTTC[A/G]GTTCCCACCTATGAG | 90293 |
rs190387820 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014509 | ACCCTCATCAGTATT[A/C]TAATTTTGCCTTTGC | 90293 |
rs190396602 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027684 | ACACTTTCATACATG[C/T]CCCACCTTTCACACT | 90293 |
rs190402452 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040724 | GTTACAGAACATCAA[A/G]TAGATTTAGCTCAAA | 90293 |
rs190406633 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021208 | ATAATGTCCTCCACG[A/T]TCATCCATGTTGTTG | 90293 |
rs190411735 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117899591 | TTTTCATCTTCTTAA[A/G]GAACAAAACAATTAC | 90293 |
rs190437540 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959276 | GAAAGTGATCGTAAC[A/G]AATGAGAAAATCACT | 90293 |
rs190452007 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117908197 | TTCTTTCTTTCTTTC[C/T]TCCTTTCTGTCTTTC | 90293 |
rs190454369 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117939102 | CCTAGCCCCCCACCC[A/C]CTGAAAGGCCCTGGT | 90293 |
rs190456514 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117962201 | GGCGACACAGTGAGA[A/T]CCCCATCTCAAAAAA | 90293 |
rs190460132 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117990471 | TGAAACAATATCTCC[C/T]AAAAGCAGTCATTTT | 90293 |
rs190464947 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117993303 | GTGACATTCAAAAAG[A/T]CTTTTAGGAGACAAA | 90293 |
rs190468077 | snp | C/G | 2.29885e-05 | 0.00339024 | intron-variant | KLHL13 | GRCh38.p7 | X:117919501 | TACCACAGGAAAAAT[C/G]AGATTTCAAAATATC | 90293 |
rs190479115 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953878 | TATTTCCATAAAAAC[A/G]ATACCAACACTAAAA | 90293 |
rs190480326 | snp | C/T | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:118019383 | GCTCATTGTAGATTC[C/T]GGATATTAGCCCTTT | 90293 |
rs190485321 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117975800 | AAACATTGATGAGTG[A/G]AAAACAGGCAAGTTA | 90293 |
rs190487303 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936533 | TAATTCATTAACTAT[C/T]TTCTGTTTTCTTCAA | 90293 |
rs190493864 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117991514 | TTATTCAAAAACTTT[C/T]CATGACTCCTTATTT | 90293 |
rs190495594 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007599 | CCCTAAAACAGACTG[C/T]AAAGGTCACTAGAGG | 90293 |
rs190504221 | snp | C/G | 0.127347 | 0.217844 | intron-variant | KLHL13 | GRCh38.p7 | X:118020626 | ATACCATTTGACCCA[C/G]CCATCCCATTACTGG | 90293 |
rs190516151 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118033090 | GAAATGTAGGACTAT[C/G]TGAAAAGACCAAATC | 90293 |
rs190555023 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118111875 | CCAGCCTGAACGATA[A/G]AGTGAGAGAGCGAGA | 90293 |
rs190570545 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096401 | TTGAATCTCTGAATA[C/G]ACCAATAACAGGCTC | 90293 |
rs190574669 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083087 | ATACAAATTGTAAGA[C/T]TGTTTTTCTCTTGTT | 90293 |
rs190587033 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118065362 | GTAGACCCAGCACCC[C/T]TCTCAGTCTCTGAGA | 90293 |
rs190601155 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118051175 | ATACCACCTACCTGA[A/G]AGCAGCAAAGTTTGT | 90293 |
rs190628595 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118057193 | CAGAAATAAAGCCAC[A/G]TGTCTATGGTTAACT | 90293 |
rs190686751 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922512 | GTAACTTTAAAGCCA[C/T]GTAGTCACATTGGGT | 90293 |
rs190695884 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947166 | AACAACTTTTGTGGA[C/G]AGACGTTTAAAATTA | 90293 |
rs190702323 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117978944 | ATTTTATTTTTTTTA[G/T]TTTTGAGACAGAGTC | 90293 |
rs190718464 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:117901340 | CATGGGGACTGGAAA[A/G]CAAAATTTGAATGCT | 90293 |
rs190729165 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117922915 | TATATCATAATCTAC[A/T]TTATGCTTGTATTAA | 90293 |
rs190735257 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955888 | TTAGGAGATGCAAAA[A/T]GTCTTCACTGTTACT | 90293 |
rs190807915 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118036663 | AAACATAGGCATTAC[C/T]ATTCAGGACATAGGC | 90293 |
rs190824241 | snp | G/T | 0.00158814 | 0.0281345 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118072 | ACACTGAAATTCTAG[G/T]AGTAGGTTTTAGGTA | 90293 |
rs190842704 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118065804 | CTCAACTAAGACAGG[A/T]ATAGGTAATGAAACA | 90293 |
rs190847536 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117913278 | AAATGGATACATGTG[C/T]TTGTTTATCCACTGG | 90293 |
rs190854301 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118082377 | TGTTGAGCATTTTTT[A/T]AATATATCTGTCAGC | 90293 |
rs190855479 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:117934714 | TGTGTGTATGAACCC[C/T]TACTACTGAGTAATA | 90293 |
rs190858326 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064837 | AGGATAACAACGCCT[A/G]CTTCTCAAAGGGTGG | 90293 |
rs190863635 | snp | A/C | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:117966786 | CTGATCTTTGACAAA[A/C]CGGAGAAAAACAAGC | 90293 |
rs190864533 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094094 | GAGCTAAAGGAGGAA[A/G]TTCGAACCTCCTCCT | 90293 |
rs190866041 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117953459 | CCTAATGCTAAATGA[C/T]GAGTTAATGGGTGCA | 90293 |
rs190869682 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118049642 | GTATGCTCCCACACA[C/T]GCACCCTAACAAAAT | 90293 |
rs190880956 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118061760 | CATTATTAAATTCGT[A/G]GAGACATATGAACCA | 90293 |
rs190883758 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117983380 | ATTACTGTAACTATA[C/T]TTGATAACTGTCTTC | 90293 |
rs190888022 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117999219 | AAGGATTATAAATCA[C/T]GCTGCTATAAAGACG | 90293 |
rs190893944 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118014301 | TAGGTCTATAGATGG[C/T]TGCTCTGGAAGTGTC | 90293 |
rs190906028 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118026653 | AAAGATGAAGCCCTC[A/G]GCAGCAGATGATCCA | 90293 |
rs190962370 | snp | A/C | 0.0183711 | 0.0940641 | intron-variant | KLHL13 | GRCh38.p7 | X:118103569 | AGAAGAAAAAGAGAG[A/C]AACCTAAGATTAACA | 90293 |
rs190988342 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915703 | GTAATCTTTTGAGTT[C/G]AATTACAGATGCCCT | 90293 |
rs190990862 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939673 | TGTGGTTTTGATTTG[C/T]ATTTCTCTAATGACC | 90293 |
rs191004046 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117971046 | CAGGTCAAAGAGGTA[A/C]GCACTTAAAAGGAAG | 90293 |
rs191018205 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117988429 | CTTAAGTGGTTTACA[G/T]AATTTTCTGTCCTGC | 90293 |
rs191019955 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117971923 | CTTTAAAAAAAGATT[C/T]GGTTTTCCTCCACCA | 90293 |
rs191032625 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004155 | GAAATCATGAAAAGG[A/G]AGAAAACTAGAATGA | 90293 |
rs191041898 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118018628 | TTCTTAGCATTCAGT[C/G]TTTTATCAAGAACCA | 90293 |
rs191046309 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118031707 | GATCATATATATAGA[C/T]AAATATATATTTGAA | 90293 |
rs191048564 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118003390 | CCAGCTTTGCTGATA[A/G]TTTATATTTATCACT | 90293 |
rs191053864 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117980970 | GCAACCTGGTCAATA[C/T]TTCTATTTTCATGAC | 90293 |
rs191063947 | snp | A/C | 0.0157677 | 0.0873799 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031103 | AAATAACTCATGTAT[A/C]CAATCTCATGACACA | 90293 |
rs191088120 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117900897 | CTACAGGAGAATGAA[A/G]GCAGAAAATGCATTA | 90293 |
rs191108612 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930334 | AGGAAGGCAGGAAGG[A/C]AGGAAGGCAGGCAGG | 90293 |
rs191117621 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117915534 | GGGGGGAAAACACAA[C/T]TAAAAAATTATTTTA | 90293 |
rs191121839 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117949338 | TTTTTTTTAATAGCA[A/G]GCAACATGACAATGA | 90293 |
rs191122272 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078270 | TAGGTTTATTGAGGT[A/G]TAATTTACATATAGA | 90293 |
rs191123029 | snp | A/G | 0.0374181 | 0.131563 | intron-variant | KLHL13 | GRCh38.p7 | X:118099902 | GAAGGAAAGAAGGAA[A/G]GAAAGAAGGAAGGAA | 90293 |
rs191134847 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118068538 | CAAAGGTAGGCAAGA[A/G]GATCCCAGCAGCCCC | 90293 |
rs191137526 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044507 | TAGAGCTACAGTAAC[C/T]AAAACAGCATGGTGC | 90293 |
rs191273853 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935673 | TTCAAACAACTAGAT[C/G]TCTTGAGAACTCACT | 90293 |
rs191276223 | snp | A/G | 0.0194105 | 0.0965841 | intron-variant | KLHL13 | GRCh38.p7 | X:117905820 | GAATAATCCAATTAT[A/G]TATACTCATACTTAT | 90293 |
rs191296380 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117964944 | ATGGCTGCATAGTAT[C/T]CCATGGTGTATATGT | 90293 |
rs191297918 | snp | A/C | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:117965405 | TGAGAAGTGTCTGTT[A/C]ATATCCTTCGCCCAC | 90293 |
rs191298557 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018060 | CTGTTTCCATCAAAG[A/C]AAACCACATGTGGCT | 90293 |
rs191300743 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117996703 | CCAGGCTTTTTTTCC[C/T]AATCAGCGTTAAAAT | 90293 |
rs191301513 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117951944 | CCATGTTCATGGGTA[A/G]GAAGAAACAATATCA | 90293 |
rs191303729 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118102194 | GTAGCTGATGTCATA[C/G]AGATAATATCTCCAG | 90293 |
rs191305092 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117967304 | CAATACATCATGGCA[G/T]CCATGTCAATCTAAA | 90293 |
rs191305562 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982311 | CAAAACTCACTTATT[C/T]TTCACCTTTTGGCAG | 90293 |
rs191309821 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118089237 | GAAGAGGCCCAGTGG[A/G]GAGCCAGGACTTTCA | 90293 |
rs191316334 | snp | G/T | 0.0131573 | 0.0800346 | intron-variant | KLHL13 | GRCh38.p7 | X:118070878 | GTCATCTAGCATTAG[G/T]TATATCCCCCAATGC | 90293 |
rs191319355 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117999629 | GCACACCAACATGGC[A/G]CATGTATACATATGC | 90293 |
rs191322678 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998123 | GAGAACTCACAGTTA[A/G]GGTGGTGGGACATGA | 90293 |
rs191324532 | snp | G/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118056859 | TTTGTTGTGAGGATA[G/T]ATGAACAGCTGACAT | 90293 |
rs191324872 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013459 | CTAGCATGGAAAGCA[A/G]CAATGGAAATATATT | 90293 |
rs191338905 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118026117 | GGAAAATTCCTTCTA[C/T]GGTATCTGTCAAGTA | 90293 |
rs191345366 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118038041 | GAATAAGGAAAAATA[A/T]TGAAAAAAGGAGAAC | 90293 |
rs191358109 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118112002 | TACCCCTTTTTTACA[C/T]ATGAGATAACTGAGG | 90293 |
rs191366743 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118086343 | TTGAGAAATCTCTAG[A/T]CTGTTTTTCTTAGAG | 90293 |
rs191377955 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118083958 | AAAAATCAAAGAAAG[C/T]ACAAATGGAGAAATA | 90293 |
rs191388327 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118054104 | ATTTTATAGGGAAAA[C/T]TAAGTGGCTTCATGT | 90293 |
rs191391677 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078928 | CTTGCCAGCACCTTC[A/G]CATTGTCAGTTAGGT | 90293 |
rs191409547 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117924351 | TAAAAGAAAAAGAGA[A/G]AGGTTCATTATCTTC | 90293 |
rs191425845 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053796 | GTGTGTGTGTGTGTG[A/T]GTGAGAGAGAGAGAG | 90293 |
rs191521531 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117919261 | ACTCCCAACCTTAGA[A/C]GATCTGCCCGCCTCG | 90293 |
rs191525301 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953544 | TGTACCCTAAAACTT[A/G]AAGTATAATAGTAAT | 90293 |
rs191537237 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117926210 | GGGATCTGTGAAAGA[C/T]AAGAAACAAATTGGG | 90293 |
rs191542483 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117984242 | TTTTAAAAATAGAGA[A/C]CACTACAGAAGCACT | 90293 |
rs191543191 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117960260 | TTAAAATACCATCAA[G/T]CCCCTGCACCTGCCA | 90293 |
rs191582230 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117985046 | ATAAAATTCCCTTAG[A/C]AATCTTATTCAAAAT | 90293 |
rs191597011 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033175 | AACACTCTGCAGGAT[A/G]TTATCCAGGAGAACT | 90293 |
rs191598526 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118014918 | TCAAAATATTCAAAA[G/T]CTAATAAGAAAAACA | 90293 |
rs191614187 | snp | A/C | 0.0864922 | 0.189117 | intron-variant | KLHL13 | GRCh38.p7 | X:118096623 | TGGCAGAGACACAAC[A/C]AAAAAAGAGAATTTT | 90293 |
rs191619141 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041729 | CATATCAAAAAACAT[A/G]TATCAGATATATAAA | 90293 |
rs191625493 | snp | A/C | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:118038336 | AACTTTCATAACAAC[A/C]AAAAATCAGGTGAAT | 90293 |
rs191630016 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045841 | TAAAACTACACTGAG[A/T]TATCATCTCATCTCA | 90293 |
rs191631730 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094291 | AAGAAAGGGTATCAG[C/T]GATGGAAGACGAAAT | 90293 |
rs191656229 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117924845 | TCCTGGAAAAATAGC[A/G]TCATTTAATGCTATT | 90293 |
rs191661147 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117910469 | TGGGAAAATAGAAGG[C/T]TGTTCTATTATGATT | 90293 |
rs191665582 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117942467 | TGTGGGAGTCTAAGT[C/T]TCTTTGTAGATCTCT | 90293 |
rs191677325 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973498 | TTATGGGAAAAGCCC[A/G]TTTCAAAAATTCCAG | 90293 |
rs191681706 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958207 | TGAAACTATGGATAT[A/G]CCAAATTCCATATAC | 90293 |
rs191689034 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117989209 | AGTTTATTATACCTC[C/T]TTATTTTTAACAGTT | 90293 |
rs191691844 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118005351 | TGAAAACAGCCATTA[C/T]CTTAATACCCTCCAA | 90293 |
rs191781297 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117912829 | TTTCTATAGCTCATA[C/T]ACAACAGCTACTATA | 90293 |
rs191792608 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944901 | ATTACATGTATCAGA[A/G]GGTTTGCATCCAGCA | 90293 |
rs191832484 | snp | A/G | 2.28862e-05 | 0.00338269 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117945464 | ACTGTGGGTATTGCT[A/G]GTAAAGATGCGTGTA | 90293 |
rs191836701 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117978178 | TTTTGTAGCTATGAC[C/T]ATGCCTTGGATTTAT | 90293 |
rs191851655 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118104764 | CCTCTTTGTGGCCAC[A/G]TTTGTTTCAAAACAA | 90293 |
rs191863824 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008166 | ACTGTTGTTCAGGAG[A/C]CTTTGAAAATTTTAC | 90293 |
rs191864069 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118093123 | CTGCTAAAAGTGCCT[C/T]CACTAGTTGATAACA | 90293 |
rs191864500 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118075661 | CCAGTGACATGGAAT[A/G]AAAGAGGAAGGGGGA | 90293 |
rs191868233 | snp | A/C | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:117907747 | TCATGCGACATAGTC[A/C]AACAATCTAGAAAAT | 90293 |
rs191868353 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117913452 | TTCATCTGAGTTCAT[A/C]TTTTATTTCATCTGA | 90293 |
rs191872037 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117946131 | AAAGATTAATTGTTA[C/T]ATATTAATGCATTAC | 90293 |
rs191873031 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118059485 | GAGCACAGTCAATGA[C/T]GACATCCATTTTAAG | 90293 |
rs191875611 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118033140 | TGAAAGTGAGGGGGG[A/G]GAATGGAACCAAGTT | 90293 |
rs191877394 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118043247 | TGCAACTGTAATAAA[A/G]TGTCTCCAGCACAGG | 90293 |
rs191880148 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117928179 | TGTGTTTAATAGCAG[A/G]GTTTCAAAATACATG | 90293 |
rs191880842 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000660 | AATTCAAACACTTGG[A/C]AATCAATTTTTTCTT | 90293 |
rs191889939 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117961561 | ACTTTGAAATGGGGC[A/G]TGTCTTGTTTTATCC | 90293 |
rs191897468 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978367 | TAAGATAAGAAGGGT[G/T]CCATGTTGGGCAGAG | 90293 |
rs191897756 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117992275 | GGGTCATAGGAGAAC[A/T]ACAAATCTCAATTTC | 90293 |
rs191905881 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118028065 | ACAGGACAATCCTAT[C/T]TTTAAAAATGTGTTG | 90293 |
rs191911656 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008604 | AAAAGATCATCATGA[C/G]AAGTATTTATTACTG | 90293 |
rs191921020 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074118 | GATTACTGGAATGTT[C/G]TACCTGTATAAACTG | 90293 |
rs191923683 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104230 | CTGTCTCAAAAAAAA[C/G]ACATTTTCCATAACA | 90293 |
rs191928809 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096267 | CACCGATCCCACAGA[A/T]ATACAAACTACCATC | 90293 |
rs191955510 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032511 | GGCCAGGTACTCCAA[A/C]AGACCTGCAGCTGAG | 90293 |
rs191976191 | snp | A/C | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118050424 | TTACAAACATTCATT[A/C]AGTATCAAATGCCAG | 90293 |
rs192027983 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117909201 | AAAATAAAACCCTAA[C/T]TACATTTTTATCTGA | 90293 |
rs192044206 | snp | A/C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117940661 | AGAGGTCCTTCACAT[A/C/T]GCTTGTAAGTTGGAT | 90293 |
rs192049733 | snp | C/T | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:117964071 | GGGGGAGGGATAGCA[C/T]TGGGAGATATACCTA | 90293 |
rs192061443 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117995356 | CCCATAAAATGTCAC[A/G]CATACCACACTACTG | 90293 |
rs192068022 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117906334 | CAACTAACACAAATT[A/C]ATTTTTTATTTATAT | 90293 |
rs192073846 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118022633 | GCCATTTTTATGTAT[G/T]ATTTTTTAAAATATA | 90293 |
rs192100647 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117905108 | TCTAGAAACATAGAA[C/T]GCTGGTGAGTGATCA | 90293 |
rs192134333 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118107431 | GACAATATAAACAAA[G/T]AAGACACACAATTTC | 90293 |
rs192143921 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117961045 | GCATCTTCAATTTCA[C/T]TCATATCTGTATTTT | 90293 |
rs192150935 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991772 | TGGGGGAGGGAGGTG[A/G]AGAAGAAAGGAAAAT | 90293 |
rs192169318 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118059261 | AAAATGAAAAATACA[C/T]TGATATTAAGGAGAT | 90293 |
rs192170055 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118113952 | TGATACATAAAAACC[C/T]GATTGTTATGAATAT | 90293 |
rs192172949 | snp | A/C | 0.0615552 | 0.164282 | intron-variant | KLHL13 | GRCh38.p7 | X:118020888 | CAGCAAACTATCACA[A/C]GGACAGAAAACCAAA | 90293 |
rs192180599 | snp | A/G | 0.0317957 | 0.122012 | intron-variant | KLHL13 | GRCh38.p7 | X:118098310 | ATTTATGCAGCCAAA[A/G]GACACATGAAAAAAT | 90293 |
rs192183981 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117993026 | GTTACAGTCACAGTA[C/T]TATATAAGCTATGCT | 90293 |
rs192186876 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118008996 | CAATACAACTACTAT[G/T]AGTACTGGGACTTCA | 90293 |
rs192198674 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085379 | GCCAGGAACTGGGGA[A/G]AGGGGAGATAGACTT | 90293 |
rs192200969 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118021511 | TTTCTGTCCTTGTGA[C/T]AGTTTGCTGAGAATG | 90293 |
rs192210646 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033569 | ACCACCAGGCCTGCC[C/G]TAAAACAGATCCTGA | 90293 |
rs192213086 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118001709 | TCTCTACCAAAAATA[C/T]GAAAAATTAGCTGGG | 90293 |
rs192217409 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118092046 | TGATACATTAGACTT[G/T]GGACACTCAGGAGAA | 90293 |
rs192225817 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118111697 | GAAGATCGAGACCAT[C/G]CTGGCTAACATGGTG | 90293 |
rs192241707 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118058930 | AAGCACAAATGCACA[C/T]TCATGTTAGTAACTG | 90293 |
rs192312338 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117957109 | CATTTCCCATGTCCA[A/G]TCAACTGCTAAGTTC | 90293 |
rs192328997 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117932838 | TCCACCAACAGTATT[G/T]AAGAGTTCCCTTTTC | 90293 |
rs192334536 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117988897 | TACGAAATATACCAA[C/T]TTATATTTTACTCAC | 90293 |
rs192354838 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118018866 | ACTCATTAGTTCTAG[C/T]ACTAAGGGGTTGTTT | 90293 |
rs192363127 | snp | C/T | 0.0850455 | 0.187856 | intron-variant | KLHL13 | GRCh38.p7 | X:118095567 | CTACAGAACTCTCCA[C/T]CCCAAATCAACAGAA | 90293 |
rs192364958 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968288 | GCAGCCTTGGTGAGG[C/T]AGTGAGCCCTTTGTC | 90293 |
rs192365077 | snp | A/G | 0.0026455 | 0.0362733 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897513 | CTCTTGAAGATCAGG[A/G]AGACTAAACTCGGAA | 90293 |
rs192371527 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117954101 | AATGATATTCCATTA[C/G]ATAACTATAACAGGA | 90293 |
rs192371551 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913797 | GCTGTGAGCCAAGAC[C/T]GCACCACTGCACTCC | 90293 |
rs192375569 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117947270 | AGATTATATTAATAG[A/G]ATATTCAAGCAGACT | 90293 |
rs192381990 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063385 | GTCTCAAAGCTTACC[A/G]ATGAGAAAAACATTA | 90293 |
rs192382628 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985634 | TCTTTGGAGCAAAGG[A/T]GGAGTGAGACAAATA | 90293 |
rs192388372 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118001077 | AGGATGGTCCTTTGT[A/T]ATCAATAAAGTTAGC | 90293 |
rs192398487 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118016222 | ACACCACTTGACAAA[C/T]AGTAAAGGCTAAATA | 90293 |
rs192406591 | snp | A/G | 0.00630859 | 0.0558077 | missense, intron-variant | KLHL13 | GRCh38.p7 | X:118028431 | AAATATACCGGTTAC[A/G]AAGTATTGCAGCAAC | 90293 |
rs192409176 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117980341 | AAATACCTATACTTT[C/T]CTAAAAGTCTGAATT | 90293 |
rs192413679 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118042537 | AGAATATAACTAGAA[A/G]TCAATAACAAGAGAA | 90293 |
rs192414558 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924123 | TTAGTGAATTTTATT[A/C]TACGTTATGTCTATC | 90293 |
rs192424866 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117956834 | TCCATGAGATACTTG[C/T]TGAAGCAATCATCAT | 90293 |
rs192428321 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118011554 | AATCTAAGGAAGTGA[C/T]AATAAGGATAAAACA | 90293 |
rs192445599 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097821 | TGGAGGAAAACAAGC[A/G]ATGGGGAAAGGATTC | 90293 |
rs192452649 | snp | C/T | 0.32348 | 0.238958 | intron-variant | KLHL13 | GRCh38.p7 | X:118036434 | AGCCCTCAGAAACAA[C/T]GCCGCATATCTACAA | 90293 |
rs192459868 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118084215 | ATGCACCTGTAGTCC[C/T]ACCTGCTCTTGGGAA | 90293 |
rs192465783 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118066065 | GACAGGTAATATTTA[C/T]TTAGTAGTGGAGGTG | 90293 |
rs192470527 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118051390 | CTGAAAATACAAAAA[A/T]ATTGGCCGGGCGTGG | 90293 |
rs192582230 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:117951374 | TTCTCTCTCTTTTTT[C/T]TTTTTCAAATACCAA | 90293 |
rs192617958 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118101753 | CAGGTGCAGTTTTCC[C/T]CATGCTGTTCTCGTG | 90293 |
rs192624772 | snp | A/C | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117902674 | TAAGTATCTTTCAAT[A/C]AGTCTGTTATAACCT | 90293 |
rs192626380 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117916513 | AGGTTGGCTCTTGTT[C/G]CATTAACACTGATGC | 90293 |
rs192631251 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117951681 | ACAGGCTTCTTATAT[A/G]CATATGTCTGTCACA | 90293 |
rs192638875 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117932246 | TTACATTGTTATTTA[C/T]TATAGTCACCCTACT | 90293 |
rs192641967 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118070461 | CCAGAGAATATACTC[A/T]AATTTTCAGTCCTTT | 90293 |
rs192643509 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118032295 | TGGGGGCAGGGCACA[A/G]ACAAACAAAAAGACA | 90293 |
rs192650959 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117965047 | ATGCCGCAATAAACA[C/T]ACATGTGCATGTGTC | 90293 |
rs192661228 | snp | C/T | 0.0105399 | 0.0718252 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118741 | TTATCCAATAGAAGT[C/T]CATTGCTGTTTGGGT | 90293 |
rs192667247 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080866 | GAATCAACCTAGGTG[C/T]CCATCAATGGTGGAC | 90293 |
rs192676336 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118101283 | GACATCTTAATCAAG[A/G]AGTCATAATTAGTAA | 90293 |
rs192678383 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118063537 | CTTTCAGAACAGAAA[G/T]GCTGAGAGCAGTTTG | 90293 |
rs192680133 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117989335 | TCAAGTGACATAGCC[A/G]CTGAGAGAAGTGGAA | 90293 |
rs192683095 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087415 | TATACACATATATAT[A/G]TCTTCTGTGAGTACA | 90293 |
rs192687477 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118005622 | GTGAGAAAGATTTGA[A/C]CCAGCACTGCTGGCT | 90293 |
rs192689198 | snp | A/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118047146 | TGTGTTTATTTTTTT[A/T]AAAAAGCAGAGGTTA | 90293 |
rs192692819 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118019363 | TTTCTTGTAAATTTG[G/T]TTGAGCTCATTGTAG | 90293 |
rs192710426 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117916820 | AATATCACTATATCA[G/T]TAAAAACATAAAGCC | 90293 |
rs192714449 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117941183 | TGTCAAAGGCCTTTT[C/T]TGCATCTATTGAGAA | 90293 |
rs192715001 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:117972183 | ACAAATTCAAACTTA[C/T]ACTTCAGAACTTGAA | 90293 |
rs192721813 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118004322 | CTCTCCATCAAAAGG[C/G]CCTTGGAACAGCAAT | 90293 |
rs192725631 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118108920 | CAAGGGATCCTCCTG[C/T]CTAAACCTCTCGAGT | 90293 |
rs192736562 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | KLHL13 | GRCh38.p7 | X:118031874 | AGTGGGTGCAGGCCA[A/G]TGGCTGCGTGCACCG | 90293 |
rs192743010 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080065 | AATGGTGCTGGGATA[C/T]TTGGCTAGCCATATG | 90293 |
rs192750129 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047076 | CTTTCAAACAAGTAA[C/G]AGAAGGGGGGATGAT | 90293 |
rs192768072 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117937912 | TCCCCCCAATTTCCC[C/T]AGCTGTAAGCAACCA | 90293 |
rs192778927 | snp | C/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118115228 | GTCTATTTCCAAAAA[C/T]ACAGCTGCGTATGTC | 90293 |
rs192784305 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968736 | TCAATTTAATAAGTA[C/T]TTTGCTAGATAAGAA | 90293 |
rs192789199 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001265 | CTTTGGAAACTTTTC[A/G]TAGTCTGGGGCAGGA | 90293 |
rs192799368 | snp | A/G | 0.00317376 | 0.039709 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029206 | GAAGTTAGAAGGGGG[A/G]AGTTGAGGCAAATAC | 90293 |
rs192806809 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055254 | AGAAACCATCTTATG[A/G]AACACATTCAGACCC | 90293 |
rs192834751 | snp | A/T | 0.0331247 | 0.124359 | intron-variant | KLHL13 | GRCh38.p7 | X:117901981 | AAGAAAATTATTTTT[A/T]ACTTCAAATTTAGCA | 90293 |
rs192834985 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117931622 | TTTTAGCCTTTGCTA[A/C]TACATGTTTTTACAT | 90293 |
rs192861980 | snp | A/T | 0.00211696 | 0.0324653 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118974 | TTGCATTTGGAGAAA[A/T]GGTCTTTAAAGAGGT | 90293 |
rs192868918 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088312 | TGATCACTAGTTAAC[C/T]GGTACTGCAATAATG | 90293 |
rs192871257 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118019190 | AATTTTCATGCTTTG[A/T]CCTTCTTCTTCCCAT | 90293 |
rs192876394 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118055896 | CCTCTATTCAACATT[C/G]TGCTAGAAGCTCTAT | 90293 |
rs192900824 | snp | C/T | 0.0292288 | 0.117303 | intron-variant | KLHL13 | GRCh38.p7 | X:117928724 | TATATCAGTCAATGA[C/T]TATATTAAAAAAGAA | 90293 |
rs192906229 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117962136 | GGATCACTTGAGTCC[A/G]GTGGTCGAGGCTGCA | 90293 |
rs192926675 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118066619 | GAAAAACATGATCTA[C/T]GAAAGAGAAACCTGA | 90293 |
rs192929607 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092274 | AATCAAACTTTTGAA[A/G]GTTGTTAACAAATAA | 90293 |
rs192933144 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118017228 | ACCTCCCTCTCCTAA[C/T]TCATCTCCAGCCTTT | 90293 |
rs192978614 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921330 | GATACCCCATTTACC[A/G]TGATGTGATTAAAAT | 90293 |
rs192980638 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117954494 | AATCCATTCTATTTT[C/T]TGAATGAGATAATTA | 90293 |
rs192989784 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099042 | TGCAGCACACCAACA[C/T]TGCACATGTATACAT | 90293 |
rs192995660 | snp | C/G | 0.00949095 | 0.0682305 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985809 | GCCAGTCATTAAGTC[C/G]TATCTTTTTTTCTTT | 90293 |
rs193000879 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118016881 | AGAACCTTCTGCCTA[C/G]AGTGTGAAGAAACCA | 90293 |
rs193020809 | snp | C/T | 2.28256e-05 | 0.0033782 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117920359 | TCCTTCAAGTCGAAG[C/T]TGGTCAAAGCCCTAC | 90293 |
rs193042794 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118105004 | CTGTCAGTAAAAAGA[C/T]TGTCAATTTGTTTTA | 90293 |
rs193048077 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117978971 | AGTCTCATTCTGTAG[A/C]CCAGGCTGGAGTGCA | 90293 |
rs193054644 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076510 | ACTGCAGTCGTTGCA[C/T]TGGGAGAAGGACTGG | 90293 |
rs193059427 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118009971 | AAGACATTTATGCAG[C/T]CAAAAAACAATGAAA | 90293 |
rs193062937 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043550 | CATCAAGATCAAATG[A/G]GTTTTGCCCCAGGGA | 90293 |
rs193068981 | snp | A/G | 0.113965 | 0.209748 | intron-variant | KLHL13 | GRCh38.p7 | X:118033615 | TGGAAAGGAACAACC[A/G]GTACCAGCTGCTGCA | 90293 |
rs193128458 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117913570 | GAACAACAAGGCCGG[C/G]GGCGGTGGCTCACGC | 90293 |
rs193138686 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118110160 | AATTAAAACCCAATT[C/T]ATATCATGGACGCTA | 90293 |
rs193139998 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117997682 | CAGATGATTCTCCTT[A/G]GAAATAATCCATGAA | 90293 |
rs193145032 | snp | C/G | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117973925 | AGGGACCACTCCAAA[C/G]CTCAACAGCGGGTCC | 90293 |
rs193145657 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025415 | CACCCCACCCACGAC[A/G]GGAATTATCTCTTTG | 90293 |
rs193156482 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117946742 | TGCTTTTCTAACTGT[C/T]TAACTGAGCTATCCA | 90293 |
rs193157747 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117978742 | TCAGAAGTTCTTGCC[C/T]TTCCTTCTTCATTTT | 90293 |
rs193170737 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074955 | ACATTGTAAACTACT[G/T]GTTCAGCCCCTTTGG | 90293 |
rs193172036 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030011 | AAAGAAAAAAGAAGT[A/C/T]ATGTGAAGATCTAAA | 90293 |
rs193211032 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117906758 | TTTTCTACAAAAGTT[C/T]AGCTACTTATAGGTT | 90293 |
rs193217604 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936997 | TGGCTGAAACCCATG[C/T]CCTTCTCACTACAAT | 90293 |
rs193227812 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117962259 | ACATTTTAGGCCATT[C/T]GTTTGCAGTAATTTG | 90293 |
rs193228698 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093191 | GTATTTCTTCTTGTA[C/T]AAACGTCTTAAATAA | 90293 |
rs193230981 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118112887 | GCCATTTGAAAATGT[C/T]GGAGAGGCAACAGGT | 90293 |
rs193231866 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117993333 | AATTGACAGGATTTA[C/T]TGACTGGAGATGATG | 90293 |
rs193232223 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060000 | GTAATTTATAGCACA[A/T]CTACAAAGAATCAGG | 90293 |
rs193235536 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118021806 | TAGATCCTTGAGGAA[A/T]CGCCACACTGTCTTC | 90293 |
rs193290593 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117958977 | TCAGGCTATCTGCAG[G/T]GCTGGATCAGCAATC | 90293 |
rs193291792 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981510 | TCAAAATCAAATATA[C/T]GTTTTAAATAATCAG | 90293 |
rs193294582 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118095746 | AGAAACTCATTCAAA[A/G]CCGCTCAACTACATG | 90293 |
rs193299542 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118037859 | CAGTCAAGAACTGAG[A/G]TAAGAGCCCAGACAA | 90293 |
rs199522673 | in-del | -/TTTA | 0.293331 | 0.246216 | intron-variant | KLHL13 | GRCh38.p7 | X:118070746 | TAATTTTTAAATATT[-/TTTA]TTTATTTATTTATTT | 90293 |
rs199525002 | in-del | -/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118014844 | AATATTAAGACATTG[-/T]TTGTACCACAGAATG | 90293 |
rs199530440 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959084 | TAGTACTGCACATCA[-/T]TTTAAAAAAAACACT | 90293 |
rs199562876 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073094 | GTGAGACACTCTCTC[-/A]AAAAAAAAAAAACCC | 90293 |
rs199622195 | snp | A/G/T | 0.00157267 | 0.027998 | missense | KLHL13 | GRCh38.p7 | X:117909666 | GTGTCAGACCTAATG[A/G/T]CAGTCCTGTCTGACT | 90293 |
rs199626524 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036543 | CTGGCTAGCCATATG[A/T]AGAAAGCTGAAACTG | 90293 |
rs199650028 | snp | A/G | 0.0157677 | 0.0873799 | intron-variant | KLHL13 | GRCh38.p7 | X:118071240 | ATGTGTCTTTATAGC[A/G]GCATGATTTATAGTC | 90293 |
rs199683629 | snp | C/G | 0.000917389 | 0.0213975 | intron-variant | KLHL13 | GRCh38.p7 | X:117920391 | ACAAGAACATGAGTT[C/G]AGTCACTAATCAAGG | 90293 |
rs199707512 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118081417 | TATAAAAAAATAAGA[A/C]TACAAATACCATTTG | 90293 |
rs199710475 | in-del | -/TG | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118104840 | AGTTGCTCAGCTCTG[-/TG]AGTATACTAAACATT | 90293 |
rs199713802 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118045329 | CAGTGAACCAAGATC[A/G]CGCCACTGCACTCCA | 90293 |
rs199722513 | in-del | -/AA/GA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089613 | AGAGAGAGAGAGAGA[-/AA/GA]AAGAAAGAGAAAGAA | 90293 |
rs199723920 | in-del | -/A | 0.114895 | 0.210349 | intron-variant | KLHL13 | GRCh38.p7 | X:118022890 | TTTGGGGTGATATCC[-/A]AAAAAAATCATTGCC | 90293 |
rs199729291 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118009854 | GGCAGTATGGCCATT[C/T]TCACGATATTGATTC | 90293 |
rs199759098 | in-del | -/A | 0.127347 | 0.217844 | intron-variant | KLHL13 | GRCh38.p7 | X:118067446 | GTAAACTAAATTTAT[-/A]AAAAAAATTTCTCTT | 90293 |
rs199761856 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118099184 | ATAAGGTTAACTTTA[C/T]ATTATTTTCAAGTAC | 90293 |
rs199807010 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114171 | TTATCAAACATCAAT[A/G]AAAATCAAACAATTT | 90293 |
rs199825145 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016128 | TGTACTATGTGCTTC[A/G]TCTTAAAAATATAAT | 90293 |
rs199842938 | in-del | -/CT | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118101639 | TGATATCGTTTGGCT[-/CT]GTGTCCCCACCCAAA | 90293 |
rs199848115 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979356 | TCAGTAGGGGTAACA[A/T]ATCCAATGCTCCAAA | 90293 |
rs199854887 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087389 | AATCTACTCTTTAAA[-/AT]ATATATATATATACA | 90293 |
rs199878347 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118033134 | TGTACCTGAAAGTGA[G/T]GGGGGGGAATGGAAC | 90293 |
rs199894460 | in-del | -/A | 0.0157677 | 0.0873799 | intron-variant | KLHL13 | GRCh38.p7 | X:117978934 | TTTTTATTTTATTTT[-/A]TTTTTTTTATTTTTG | 90293 |
rs199911005 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926798 | ATATTTCCCAGTCTA[-/C]CCCCGACCTGGACTT | 90293 |
rs199927818 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118021410 | TTACCCCACGACAGG[A/C]CCTGGTGTGTGATGT | 90293 |
rs199947657 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118091342 | ATTATCTGACAAAGA[C/T]TTTAAAGTAGCCATC | 90293 |
rs199958677 | in-del | -/A | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118069402 | GTCTTCGTTTTTAAC[-/A]AAAAAAAGTTTAAAA | 90293 |
rs199978607 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051473 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 90293 |
rs200004045 | snp | C/T | 0.000185925 | 0.00963993 | intron-variant | KLHL13 | GRCh38.p7 | X:117983433 | GAAAACCAATTCGCA[C/T]TGAAAAAAAAAAAAA | 90293 |
rs200021274 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109880 | CCACAAAACCGAAGG[-/A]AAAAAAAAACAGGCC | 90293 |
rs200051142 | in-del | -/CGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935187 | ATATTCATAGCTTTT[-/CGA]ATTCATAAAAGCCAA | 90293 |
rs200071333 | in-del | -/TTCCTTAT | 0.126889 | 0.217586 | intron-variant | KLHL13 | GRCh38.p7 | X:117981588 | ACATTTATTCATTCA[-/TTCCTTAT]TTCCTTATTCAGCTT | 90293 |
rs200086682 | in-del | -/CTAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938782 | CCTCACATACTTTTC[-/CTAT]CTGTTTGACCCCTTA | 90293 |
rs200121670 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053021 | TAAGAAGAGGCATGG[C/G]GGTGTGAGATTGGAA | 90293 |
rs200140191 | in-del | -/TTTTATTTTTATC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027512 | TAAGAAACAGTTGTT[-/TTTTATTTTTATC]TTTTATTTCCATTTT | 90293 |
rs200177916 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057898 | CCTGACAATAAATTA[C/T]ATGTAAGGATATACA | 90293 |
rs200185850 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943658 | CATGAAGTCCTCATG[-/C]TGTGTTTTTCAGCTC | 90293 |
rs200193222 | in-del | -/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915363 | CCCTATTCCTCTCTC[-/TT]GTCTCCTTCCCACTT | 90293 |
rs200207656 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939821 | AATTTGTTTAAGTTC[C/T]TTGTAGATTCTGGAT | 90293 |
rs200211768 | in-del | -/AAAGATGTT | 0.0460406 | 0.14457 | intron-variant | KLHL13 | GRCh38.p7 | X:118044174 | ACCTAAGAATTAACC[-/AAAGATGTT]AAAGACCTCTACAAT | 90293 |
rs200220640 | snp | G/T | 4.76446e-05 | 0.00488058 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972832 | TTTCAATGGCATGTT[G/T]TCACCACGGTACTAC | 90293 |
rs200237933 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118096019 | TCACAATTAAAAGAA[C/G]TAGAAAAGCAAGAGC | 90293 |
rs200257694 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951683 | AGGCTTCTTATATGC[-/AT]ATGTCTGTCACATTT | 90293 |
rs200261775 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027649 | TCTCTCTCCACACAT[-/AC]ACACACACACACACA | 90293 |
rs200266721 | in-del | -/ACTG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117977420 | AAACTTAATTTGCTA[-/ACTG]ACTAGTATAGTTTGT | 90293 |
rs200269209 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117920975 | TGTTTGAAAAAAAAC[-/A]AAAAAAAAGCCCAGG | 90293 |
rs200271336 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117905652 | CAAATGTTGCCACTG[-/T]TTTTTTTTTTAATTT | 90293 |
rs200271597 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118101205 | TCTTACAAAATTACC[A/C]AGTCCTAGCTACTGG | 90293 |
rs200297273 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118009851 | TTGGGCAGTATGGCC[A/T]TTTTCACGATATTGA | 90293 |
rs200309699 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118032636 | TAAAACCACAAAGAT[-/G]GGGAAAAAACAGAGC | 90293 |
rs200381172 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118035070 | CTCTGAATAGACCAA[A/T]AACAGGAGCTAAAAT | 90293 |
rs200388194 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118035256 | ATGAGGCCAGCATCA[C/T]TATGATACCAAAGCC | 90293 |
rs200457052 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118072374 | CCTAAAACCATAAAA[A/T]CCCTAGAAGAAAACC | 90293 |
rs200522959 | snp | G/T | 2.34071e-05 | 0.00342097 | missense | KLHL13 | GRCh38.p7 | X:117910005 | AATGCAGGAAAATTC[G/T]TCAAGACGAAACTGT | 90293 |
rs200525426 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094559 | ACAAAGATACTCCCC[A/G]AGAAGAGCAACTCCA | 90293 |
rs200551370 | in-del | -/AA | 0.0126344 | 0.0784702 | intron-variant | KLHL13 | GRCh38.p7 | X:118074135 | CCTGTATAAACTGTT[-/AA]AAAAAACTGTTTGTT | 90293 |
rs200555326 | in-del | -/AGAAAGAA | 0.499935 | 0.00569499 | intron-variant | KLHL13 | GRCh38.p7 | X:118089621 | GAGAGAGAAAGAAAG[-/AGAAAGAA]AGAAAGAAAGAAAGA | 90293 |
rs200556960 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017410 | TAATTTGAAAGCGAA[-/G]AAGGCAACATGGCTA | 90293 |
rs200561523 | in-del | -/AATA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117999709 | ATAAATAAATAAATA[-/AATA]GAAAACAAAAGGTTC | 90293 |
rs200592201 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117953766 | CAATGCTTAATTTAT[-/A]AGCACAAGGAGGATA | 90293 |
rs200608948 | in-del | -/GAGA | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117980675 | ATTTAAATTTTCTAT[-/GAGA]AAGAGCCATTTATAT | 90293 |
rs200661480 | in-del | -/TTC | 0.0328205 | 0.123827 | intron-variant | KLHL13 | GRCh38.p7 | X:118100133 | GAGCTCTGCTTATTG[-/TTC]TTCTTATTTTTGCCA | 90293 |
rs200662783 | in-del | -/A | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:118083429 | CCTGTCATTTGTGAC[-/A]AAAATTGATGAACTT | 90293 |
rs200674600 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051458 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA | 90293 |
rs200727100 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022228 | GTGTGTGTGTCACAA[C/T]TTCTTTATCCAGTCA | 90293 |
rs200742074 | in-del | -/AAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930139 | TCAGACTGGAAAGAA[-/AAG]AAAAGAAAAGAGGAA | 90293 |
rs200763767 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118019343 | TTGATGGGGTTGTTT[G/T]TTTTTTTCTTGTAAA | 90293 |
rs200775163 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117984627 | GATAAATTCAAAACA[G/T]CATCTCCTTAATGAC | 90293 |
rs200824033 | in-del | -/T | 0.254907 | 0.249952 | intron-variant | KLHL13 | GRCh38.p7 | X:118023143 | TCTTCTAGGAATTGG[-/T]TAATTTTCTCTTCTT | 90293 |
rs200891556 | in-del | -/AGT | 0.0220041 | 0.102557 | intron-variant | KLHL13 | GRCh38.p7 | X:118075459 | TTAGAAAACTGATAG[-/AGT]AATTCAAACTAAAGA | 90293 |
rs200912719 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117964731 | CCTAATGCTATCCAT[-/C]CCCCCCTTCCCCCAC | 90293 |
rs200915697 | in-del | -/A | 0.0394543 | 0.134798 | intron-variant | KLHL13 | GRCh38.p7 | X:118079781 | CAGAATTAGAAAAAA[-/A]CTATTCTAAAATTCA | 90293 |
rs200920974 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916181 | AAACAAACAAACAAA[-/C]AAAAAAAACACTAGC | 90293 |
rs200951166 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938947 | GATTAGAGGGATTTA[-/T]TTTTTTTTTATACTT | 90293 |
rs200972264 | in-del | -/T | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118067512 | TTATATGCTTTTAAA[-/T]TTTTTTTAACTTTTT | 90293 |
rs200991244 | in-del | -/TAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979806 | ATATATATACTTTCT[-/TAAA]TAAAATAAATATTCC | 90293 |
rs201025398 | snp | C/T | 0.000275738 | 0.0117385 | intron-variant | KLHL13 | GRCh38.p7 | X:117899434 | TGAAGTAAATAATTA[C/T]AGAAATGCAAAAGTA | 90293 |
rs201029041 | in-del | -/T | 0.159988 | 0.233233 | intron-variant | KLHL13 | GRCh38.p7 | X:117983109 | AAGAAGGCAGAAGAG[-/T]ACAGAGCTAGGCATC | 90293 |
rs201050910 | in-del | -/CA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944934 | CCTAACCTCTTCTCC[-/CA]CAGTTACTACTACCA | 90293 |
rs201051838 | in-del | -/A | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:117998479 | AAGTAAAGAGATTCT[-/A]AAAAAAAAACACAAG | 90293 |
rs201097633 | in-del | -/A | 0.0363984 | 0.129901 | intron-variant | KLHL13 | GRCh38.p7 | X:118000609 | TTTTACAAAGTAAGG[-/A]CATTTTAAAAGGCAA | 90293 |
rs201099536 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118095828 | GGCAGAAATAAAGAT[G/T]TTCTTTGAAACCAAT | 90293 |
rs201100690 | in-del | -/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948634 | GACTATATTAACGAA[-/TT]TTGTTTCTAAAAATT | 90293 |
rs201117714 | in-del | -/AAGG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930187 | AGGGGAAAGAAAAGA[-/AAGG]AAGGGAGGGCAAGAA | 90293 |
rs201120759 | in-del | -/A | 0.0590711 | 0.161388 | intron-variant | KLHL13 | GRCh38.p7 | X:118014927 | TCAAAATCTAATAAG[-/A]AAAACAGGGAGGTAC | 90293 |
rs201137544 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117913744 | GCTACCTGGGAGGCT[A/G]AGGCAGGAGAATCAC | 90293 |
rs201138519 | in-del | -/ATACAC | 0.00211696 | 0.0324653 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031454 | TTTAGATATATATAT[-/ATACAC]AGATATATATATTTA | 90293 |
rs201146138 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117949404 | GGCCAAAGCAAGAGT[-/G]CTCTGCTGATCTGAC | 90293 |
rs201156450 | in-del | -/ATTCCTT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981587 | TACATTTATTCATTC[-/ATTCCTT]ATTTCCTTATTCAGC | 90293 |
rs201170363 | snp | C/T | 0.000115103 | 0.00758538 | intron-variant | KLHL13 | GRCh38.p7 | X:117919473 | TGAGTCCTAAACAGG[C/T]TACATCAGAGTCTAC | 90293 |
rs201214877 | in-del | -/AT | 0.125973 | 0.217065 | intron-variant | KLHL13 | GRCh38.p7 | X:118053658 | TAAAAAAAAGAAAAC[-/AT]AATGAAACAAAGGTG | 90293 |
rs201226351 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118084170 | CAAAAAAAAAAAAAA[-/A]TGTTTAAAAACTTAG | 90293 |
rs201232456 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118033194 | TCCAGGAGAACTTCC[A/C]CAATCTAGCAAGGCA | 90293 |
rs201239515 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117980517 | ATGAGGTTAGAAGAT[A/C]ACCTGGTTATCCAAT | 90293 |
rs201254163 | in-del | -/A | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:118041513 | CAGCCTGGATGACAG[-/A]GTGAGACCCTATCTC | 90293 |
rs201257925 | in-del | -/A | 0.298745 | 0.245202 | intron-variant | KLHL13 | GRCh38.p7 | X:118044433 | AAAAAAAAAAAAAAA[-/A]GGAAAATCAGAAGAA | 90293 |
rs201297076 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118012069 | CAGCACTGAAACTGA[A/G]ACCTGGCAATGTTGT | 90293 |
rs201302463 | in-del | -/T/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000562 | GAAATTTCAAAAACA[-/T/TT]TTTTGGGGTCCTACA | 90293 |
rs201310135 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089618 | AGAGAGAGAGAAAGA[A/G]AGAGAAAGAAAGAAA | 90293 |
rs201342313 | in-del | -/A | 0.0319455 | 0.122279 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898186 | TGCCACTCAATTTTT[-/A]AAAAAAATTATATTT | 90293 |
rs201356237 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903145 | GCAAAACACACACAC[-/A]ACACACACACACAGA | 90293 |
rs201399977 | in-del | -/AG | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118020436 | GCAAATCAAAACCAC[-/AG]TAAGATACCATCTCA | 90293 |
rs201431300 | in-del | -/T | 0.0349394 | 0.127471 | intron-variant | KLHL13 | GRCh38.p7 | X:118070642 | TATAACCATAATAGA[-/T]TTTTTTTTGTCTGCT | 90293 |
rs201435423 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118035077 | TAGACCAATAACAGG[A/G]GCTAAAATTGTGGCA | 90293 |
rs201439037 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010743 | CTTAAAATATAATTT[-/A]AAAAAAAAAAGAGTC | 90293 |
rs201441439 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911540 | TTCTCCTAATGCTAT[-/C]CCTCCTCTAGCCTCC | 90293 |
rs201456662 | in-del | -/A | 0.0465803 | 0.145329 | intron-variant | KLHL13 | GRCh38.p7 | X:118028393 | AATAGGAAAGACGTT[-/A]ATATAAGTTAAACTA | 90293 |
rs201467194 | in-del | -/TAGA | 0.0110639 | 0.0735497 | intron-variant | KLHL13 | GRCh38.p7 | X:118083629 | ACAAAAAGTTACAGT[-/TAGA]TAGGAGGAATAAGTT | 90293 |
rs201514400 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935210 | AAGCCAAAATGTATG[-/A]AAAAAAATGCTTATC | 90293 |
rs201550671 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118009852 | TGGGCAGTATGGCCA[A/T]TTTCACGATATTGAT | 90293 |
rs201593935 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008878 | TGATGAGTATCTACT[A/T]CATAAAGTTATTATG | 90293 |
rs201601324 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076922 | CTCTCTCTCTCTCTC[C/T]CTCTCTCCCCTTCTC | 90293 |
rs201645148 | snp | C/T | | | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909557 | CATGGGGGCTAACGA[C/T]TTCCACTCATGGGCC | 90293 |
rs201677259 | in-del | -/AGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053842 | GAGAGAGAGAGAGAG[-/AGA]GAGAGGAGAGAGAGA | 90293 |
rs201722776 | in-del | -/A | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:118100549 | TTTTTAAATTGGCAC[-/A]ATTAGACAATATGCC | 90293 |
rs201725679 | in-del | -/TTTAATG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924907 | TTTAATGTTTAATGT[-/TTTAATG]TTTAATGTTTAATGT | 90293 |
rs201725752 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916178 | AAACAAAAAAAAAAA[-/A]CACTAGCTAATGGGC | 90293 |
rs201850312 | in-del | -/ACACAT | 0.05658 | 0.158394 | intron-variant | KLHL13 | GRCh38.p7 | X:118069138 | CACACACACACACAC[-/ACACAT]ACACACACACCCTCA | 90293 |
rs201859482 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037572 | ACACAGGAAGGGGAA[C/T]ATCACACTCTGGGGA | 90293 |
rs201860376 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903511 | GCCCCAGTACTGTTG[-/T]TTTTTTTTTACTATT | 90293 |
rs201873756 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017408 | GAATAATTTGAAAGC[-/G]AAAAGGCAACATGGC | 90293 |
rs201884787 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088332 | CTGCAATAATGTATA[A/C]GTTAATCATTACTTA | 90293 |
rs201887442 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052516 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 90293 |
rs201892422 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026178 | CTCAACCTTTCCTAC[A/G]TTTTCTGTTCATTTT | 90293 |
rs201913216 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117969640 | ATGGCACACCACCCT[A/G]CAATGCTAAAATCTA | 90293 |
rs201968345 | in-del | -/AATC | 0.126889 | 0.217586 | intron-variant | KLHL13 | GRCh38.p7 | X:117978909 | GGTTGTGGTAGTGGA[-/AATC]AATCAATGGTTTTTA | 90293 |
rs201970966 | snp | A/G | 0.00483667 | 0.0489382 | intron-variant | KLHL13 | GRCh38.p7 | X:117945417 | GTAAACACTACCAAA[A/G]AGACAGCTTAAATTA | 90293 |
rs201987772 | snp | A/G | | | missense | KLHL13 | GRCh38.p7 | X:117909301 | TATAAATGCACTTAC[A/G]CAGTTCACCTGCTGC | 90293 |
rs201992185 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118009850 | CTTGGGCAGTATGGC[C/G]ATTTTCACGATATTG | 90293 |
rs202003781 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118020717 | TTGCGGCACTACTCA[A/C]AATAGCAAAGACTTG | 90293 |
rs202017763 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118054963 | ATTTTCAAATATGGT[A/T]AAAAAAAAAAAAACT | 90293 |
rs202022134 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939701 | CCAGTAATCATGAGC[-/T]TTTTTTTTCATATAT | 90293 |
rs202022749 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023145 | TTCTAGGAATTGGTT[-/A]ATTTTCTCTTCTTCC | 90293 |
rs202052483 | in-del | -/A | 0.0209675 | 0.10022 | intron-variant | KLHL13 | GRCh38.p7 | X:118032106 | GGCCCACGGAGTCTC[-/A]CTGATTGCTTGCACA | 90293 |
rs202072435 | snp | C/G | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117605 | CAGAGCGGGACTCAG[C/G]ATCCCAAGCGGTGTG | 90293 |
rs202104844 | in-del | -/AAC | 0.0388671 | 0.133876 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973297 | TTCATATGAAAATGA[-/AAC]AACAACATACCTACT | 90293 |
rs202106669 | snp | G/T | 2.29169e-05 | 0.00338495 | missense | KLHL13 | GRCh38.p7 | X:117909916 | CAAGTTCAGTACAGT[G/T]CTTAAGGCTATTACT | 90293 |
rs202114736 | in-del | -/A | 0.0251071 | 0.109193 | intron-variant | KLHL13 | GRCh38.p7 | X:118091593 | TAATTATCCAACCTT[-/A]AAAACAAAGATAAAA | 90293 |
rs202126274 | in-del | -/AG | 0.018891 | 0.0953342 | intron-variant | KLHL13 | GRCh38.p7 | X:118082305 | AATAGCAATTCTAAC[-/AG]GGGTGAGATGATATT | 90293 |
rs202142974 | in-del | -/ATA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117932470 | TTTATTTCACTTAAC[-/ATA]ATGTCTTCCAGGTTC | 90293 |
rs202158148 | in-del | -/AAATA | 0.318726 | 0.240368 | intron-variant | KLHL13 | GRCh38.p7 | X:117979807 | TATATATACTTTCTT[-/AAATA]AAATAAATATTCCAA | 90293 |
rs202181648 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118035084 | ATAACAGGAGCTAAA[A/G]TTGTGGCAATAATCA | 90293 |
rs202182642 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094113 | GAACCTCCTCCTTTA[C/G]TTCAAGGCAAAGAAG | 90293 |
rs202184691 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118096012 | CCTAACATCACAATT[A/G]AAAGAACTAGAAAAG | 90293 |
rs202210364 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118035009 | GAAATGGATAAATTC[C/G]TTGACACATACACTC | 90293 |
rs202211789 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117982319 | ACTTATTTTTCACCT[A/T]TTGGCAGAAATCTTT | 90293 |
rs202224094 | in-del | -/TAGAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117919961 | TCCTATTTTTTGACA[-/TAGAG]TAGAGATTGTACTAG | 90293 |
rs267606324 | snp | C/T | | | missense | KLHL13 | GRCh38.p7 | X:117909519 | CCAATGACGGCGATG[C/T]CATGCTGGTACCTTG | 90293 |
rs267606325 | snp | C/T | | | missense | KLHL13 | GRCh38.p7 | X:117909580 | CATGGGCCTTTTCAT[C/T]ATACATGCGCAATTC | 90293 |
rs267606326 | snp | C/T | | | missense | KLHL13 | GRCh38.p7 | X:117909850 | ATTTTGCAGCAAAGT[C/T]CATCCGAGGCTCTTC | 90293 |
rs367546564 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971842 | TTTTCCTACTGATAA[A/T]TATTTTAAAAATAAC | 90293 |
rs367548020 | snp | C/T | 6.90457e-05 | 0.00587521 | missense | KLHL13 | GRCh38.p7 | X:117945517 | AATGGGATGAGAGGC[C/T]CATTTCGCTGCCTCC | 90293 |
rs367552625 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117915643 | GTGATTTCTTTCTCA[C/T]CTTTATTCTGTTTTG | 90293 |
rs367553352 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025499 | TCAGTTAGTAGATCA[A/G]CTGCTGAGGTATTTA | 90293 |
rs367558367 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117978855 | TGTTTAAAAAAAAAA[-/A]TGCTTTAAACTCCAA | 90293 |
rs367563797 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010067 | ACCAGTTAGAATGGT[A/G]ATCATTAAAAAGTCA | 90293 |
rs367565033 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-5-prime, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117286 | CCTCACCTCAGTGGG[A/G]CCCACGTCTCAAAAT | 90293 |
rs367568157 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038273 | AAGCCTCAAGTGATC[A/G]TCTCTCCTGTAGGAA | 90293 |
rs367675802 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118094778 | ACCCAGAATTTCATA[C/T]CCAGCCAAACTAAGC | 90293 |
rs367695527 | snp | A/G | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:117963603 | TGGGATGGCTGGGTC[A/G]AATGGTATTTCTAGT | 90293 |
rs367751086 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018554 | TGCTTTGCCAAATTT[G/T]TAAATATCCTCCTAA | 90293 |
rs367753818 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118033795 | AAAGACACAGACTGG[C/G]AAATTGGATAAAGAG | 90293 |
rs367755315 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117905297 | AGCTGTCATAATCTT[C/T]TTCAATATAGGAAGC | 90293 |
rs367758426 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:117965408 | GAAGTGTCTGTTAAT[A/G]TCCTTCGCCCACTTG | 90293 |
rs367759256 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118072150 | TAGATCAATGGAACA[C/G]AACAGAGCCCTCAGA | 90293 |
rs367776397 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050704 | CCCATGGATGTTAAC[A/G]ATTTGTCTCAGCCTA | 90293 |
rs367801876 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118002511 | AGCAGGAGAATTGCT[C/T]GAACCTGGGAGGGGG | 90293 |
rs367913508 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118027171 | TGAGAAAGTTACCAA[A/C]ATATTACCAGAAAAA | 90293 |
rs367943538 | snp | C/T | 0.000147521 | 0.00858712 | intron-variant | KLHL13 | GRCh38.p7 | X:117909277 | GAAGAAATTTGTCTC[C/T]ATGCTTAATATAAAT | 90293 |
rs367949956 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117953679 | AATCCAGAGCCTACA[C/T]TGTTCCCATTTATAC | 90293 |
rs367973786 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007306 | CCCAGCTATTCAGGA[C/G]GCTGAGGTGGGAGAA | 90293 |
rs368024656 | in-del | -/ACATAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991422 | CCAAGCCAAGAGTAA[-/ACATAA]TACTCCATCATTTCT | 90293 |
rs368062193 | snp | C/G | 0.000141097 | 0.00839812 | intron-variant | KLHL13 | GRCh38.p7 | X:117945383 | ATCACAAAATCCATG[C/G]TGGGTTTTTTAAAGC | 90293 |
rs368071534 | snp | A/C | 0.0240739 | 0.107039 | intron-variant | KLHL13 | GRCh38.p7 | X:118036215 | ATCAAGCTACCAATG[A/C]CTTTCTTCACAGAAT | 90293 |
rs368079395 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076610 | TTATTTGGTGAACCA[C/T]TATTCTAGACGTTTC | 90293 |
rs368100610 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998217 | TCATTGGATTTTGAG[A/G]CATTTCCCTAAAAGA | 90293 |
rs368151729 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938519 | GACCTAGCGTTCAGT[G/T]TTTTAACAAGCCCTC | 90293 |
rs368156464 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901354 | AGCAAAATTTGAATG[C/T]TTTCCAATTTTTTCT | 90293 |
rs368164771 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049564 | AAAATACCTGAGCAC[C/T]AACTGTTGCATTGAG | 90293 |
rs368175645 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074335 | ATTTATGAGTCTGAC[A/C]TGGCAGCAGACATTC | 90293 |
rs368185496 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117964773 | CCCCAGAGTGTGATG[C/T]TCGCCTTCCTGTGTC | 90293 |
rs368187682 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994947 | TGCCTGTGAGGGACG[C/T]TGAGGTGGGAGGATC | 90293 |
rs368192209 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118035725 | CCTATTCAACATAGT[A/G]TTGGAAGTTCTGGCC | 90293 |
rs368200815 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017260 | CTTACTTTGCTCCTT[A/G]TTATTATAATTAATA | 90293 |
rs368254851 | snp | A/G | 2.29684e-05 | 0.00338876 | stop-gained | KLHL13 | GRCh38.p7 | X:117909418 | TCCATTTATTGTATC[A/G]AGGATCAAATCTGAA | 90293 |
rs368312769 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921172 | AGTTGTTCTATTGAT[A/G]TAAGTTGGAAGAATG | 90293 |
rs368338269 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030629 | AGGTGTTTAGCCATG[A/G]GGGCACCACCCTCAT | 90293 |
rs368361766 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117997408 | AATACCTGAAAAGCA[A/T]CATAATGTTCTATCT | 90293 |
rs368398505 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118116950 | CAGGGTGGCGGGGAG[C/T]CGGGGCTAGGACGGT | 90293 |
rs368414529 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010023 | ATCAGAGAAATGCAA[A/G]TCAAAACCACTATGA | 90293 |
rs368415425 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108524 | GCTCTGCTGGCCTAT[C/T]TTCAAAACCATCTCA | 90293 |
rs368446589 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117909135 | GCCAACGATATATGC[C/G]CAGATAAGGCATAAA | 90293 |
rs368456489 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117899878 | TTGCATCAGGATTGT[C/G]ACTCTGAAGTGAGAT | 90293 |
rs368466550 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025382 | GATGATGAAATCTTA[A/C]ACTATCCTACTTCAC | 90293 |
rs368476848 | in-del | -/A | 0.169962 | 0.236842 | intron-variant | KLHL13 | GRCh38.p7 | X:118011478 | AAGCAAAAAAAAAAA[-/A]CAGATTAGAAGGATA | 90293 |
rs368521454 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037207 | CTCAGGGATCTAGAA[C/G]TAGAAATACCATTCG | 90293 |
rs368593238 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118102000 | AACAAACTAATACAA[C/G]TAGCAAGTACAAATG | 90293 |
rs368606485 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117994322 | GCAGTAGTGTGATTA[C/T]AGGTGACTGCAGCCT | 90293 |
rs368634632 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117983448 | CTGAAAAAAAAAAAA[-/A]GGTGAGGAAAAATGT | 90293 |
rs368637498 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950030 | AATTAGAGAAAAGCT[A/G]GAAAGGTAAAAGTAT | 90293 |
rs368646764 | in-del | -/AAAAAAAAAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007383 | GTCAAAAAAAAAAAA[-/AAAAAAAAAAA]GAGAGAGAGACCTGC | 90293 |
rs368754862 | snp | A/G | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118410 | ATGTATCAAAAACCT[A/G]GCACACAGGTTAAAA | 90293 |
rs368764292 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028995 | ATGCCACTTGTCTCC[C/T]AGCCACTTAGTAGCG | 90293 |
rs368774073 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118067007 | AGTCATGCATCACTT[A/G]ACAATGGGGATAGGT | 90293 |
rs368781832 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118031764 | GAATAGGAACAGCTC[C/T]GGTCTACAGCTCCCA | 90293 |
rs368796360 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117931815 | CCCTGAGCTTCAGCG[C/T]CCTTATCTATAAAAT | 90293 |
rs368812622 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021990 | TCTGGTGGCCAGTGA[C/T]GATGAGCATTTTTTC | 90293 |
rs368833240 | in-del | -/GCA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083296 | CTCGTGTTTACTGCA[-/GCA]CTATTAACAATAACC | 90293 |
rs368843139 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916386 | TCATCCTTCTGTATT[C/G]ATTTCATTGTCCTCT | 90293 |
rs368909139 | multinucleotide-polymorphism | AA/TC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118090322 | CAAAAGAAACTACCA[AA/TC]AGAGTGAACAGGCAA | 90293 |
rs368924321 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118062623 | CCCTCACAGTCATAT[A/C]CTGAAATACGTACAG | 90293 |
rs368957219 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975221 | ACACACATGTATGAA[C/G]ACATCAAGTTTGAAA | 90293 |
rs368971389 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117984658 | AGTACTATTTGAAAG[C/T]ATACTTTTAAAATGC | 90293 |
rs368998133 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118043278 | AAAGTACAGGATCAG[A/C]TGGCTTCACTGATGA | 90293 |
rs369007161 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118079349 | AAAAAAGAAGTTAAA[A/C]TATCCCTCTTTGCTG | 90293 |
rs369007648 | snp | G/T | 0.0204488 | 0.0990265 | intron-variant | KLHL13 | GRCh38.p7 | X:117923920 | AGAAAAGAAGTTAAG[G/T]CACCTAGAGCATTTT | 90293 |
rs369062713 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998906 | TAACAACTATATAAA[C/T]ATATAAATTTTATAT | 90293 |
rs369141825 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118097612 | ACCAAAAAAGAGCCC[A/G]CATTGCCAAGTCGAT | 90293 |
rs369193686 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036652 | ACCCTAGAAGAAAAC[A/C]TAGGCATTACCATTC | 90293 |
rs369206979 | in-del | -/ATCAATG | | | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898766 | CAAATAACATCAATG[-/ATCAATG]TTGTCTTTTTTCCAA | 90293 |
rs369216661 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036271 | ATGGAACCAAAAAAG[A/T]GCCCGCATCACCAAG | 90293 |
rs369222768 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943288 | TCAACCTTGCTGAAT[A/C]TGACGATTATGTGTT | 90293 |
rs369240603 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053293 | GGCACATATACACCA[C/T]GGAATACTATGCAGC | 90293 |
rs369289425 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014566 | GCATGTGATCTTTTT[G/T]ACTTACTCCCTTTTC | 90293 |
rs369293914 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117966296 | CCAAATCATGAGGGA[A/G]CTCCCATTCACAATT | 90293 |
rs369297774 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986219 | GAATAACAAAAATTC[C/T]GTTGCAACTGAGGCT | 90293 |
rs369326418 | snp | G/T | 0.00014692 | 0.00856963 | intron-variant | KLHL13 | GRCh38.p7 | X:117972717 | ACTTTAATATCCTAT[G/T]TTCTCTCACTTACAT | 90293 |
rs369335644 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118020137 | TGAGCATGGAATGTT[C/T]TTCCATTTGTTTGTA | 90293 |
rs369386763 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118109453 | GCAAGCAGAGACTTT[C/T]TCTGAAATATTGGGG | 90293 |
rs369418802 | snp | A/G | 0.00021948 | 0.0104734 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117910040 | GTATTTATCCACTTC[A/G]GTTAGATTGTAGGTG | 90293 |
rs369433238 | in-del | -/GT | 0.248561 | 0.249996 | intron-variant | KLHL13 | GRCh38.p7 | X:118085796 | GAGTAATATTCCATG[-/GT]GTGTGTGTGTGTGTG | 90293 |
rs369437910 | snp | C/T | 7.97968e-05 | 0.00631601 | intron-variant | KLHL13 | GRCh38.p7 | X:117910105 | AAGTGACCTATTAAG[C/T]CAATTAAAAAAAATT | 90293 |
rs369460850 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117965812 | CAAAAACCACATGAT[C/T]ATCTCAATAGATGCA | 90293 |
rs369499141 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000044 | CTTCCATAGCTCCTA[A/T]CTCATTTCATACTTG | 90293 |
rs369522402 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089363 | GAGATATCACTGGAG[A/G]TCTAGTGAGGAGCCA | 90293 |
rs369553607 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052224 | AAAAATCGTAAAAGA[A/G]GTAGAGGGCCGGGTG | 90293 |
rs369560238 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004259 | ATATGTATAAATGTG[A/T]ATATGTATTTATGTG | 90293 |
rs369589786 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039275 | GGGTAAAGGACCAAG[A/C]AGGCTCCTACAGTCC | 90293 |
rs369599583 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118096024 | ATTAAAAGAACTAGA[A/G]AAGCAAGAGCAAACA | 90293 |
rs369642387 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118019457 | TGCCTGTTCACTCTG[C/G]TGGTAGTTTCTTTTG | 90293 |
rs369658551 | snp | C/T | 0.0399626 | 0.135589 | intron-variant | KLHL13 | GRCh38.p7 | X:118010308 | ATGTTTATTGCGGCA[C/T]TATTCACAATAGCAA | 90293 |
rs369680872 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118018254 | CCTTATTAATTTTTC[A/G]TAACAATTTTCTTCG | 90293 |
rs369732865 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082151 | AGATTGCTGTATCAC[A/G]TGGGAGATCTATTTA | 90293 |
rs369754446 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911673 | TCTGTTCCTGTGTTA[A/G]TTTGCTGAGAATGAT | 90293 |
rs369816688 | snp | A/G | 7.38871e-05 | 0.00607767 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972849 | CACCACGGTACTACA[A/G]TAACAGTAAAGAGCG | 90293 |
rs369869950 | in-del | -/G | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:118107079 | ATCAGAAAAATGTGT[-/G]ACCCCTGTGATTATC | 90293 |
rs369923085 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010267 | ATGACTATAAATCAT[A/G]CTGCTATAAAGACAC | 90293 |
rs369930000 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107130 | GTTTAAAAGATAACA[C/T]TGTTCATAGTATACA | 90293 |
rs369932090 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017338 | TGCCTTCATGCATAG[A/T]AGTGCAATGTGAGAT | 90293 |
rs369933093 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118052455 | ATGAATCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 90293 |
rs369950709 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118041658 | ATTCAGTATTAAGCC[A/G]TCAACAGTTTAAATA | 90293 |
rs369976284 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117927574 | AACTGGAAAGAATTC[C/G]GAAGATGGTCCAGGT | 90293 |
rs369987135 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027975 | CTAATTTGTCAGAAG[A/C]AGCTTTAAATATCTC | 90293 |
rs370005852 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118107917 | AATTAGCCAGGCGTG[G/T]TGGCATGCACCTGCA | 90293 |
rs370029111 | in-del | -/ACAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027669 | CACACACACACACAC[-/ACAC]TTTCATACATGCCCC | 90293 |
rs370033138 | snp | C/G | 2.2841e-05 | 0.00337934 | missense | KLHL13 | GRCh38.p7 | X:117901885 | ATGGCCATAGTGGGG[C/G]TCACTCATTTTGGCA | 90293 |
rs370046598 | snp | A/G | 4.57509e-05 | 0.00478261 | missense | KLHL13 | GRCh38.p7 | X:117909871 | GAGGCTCTTCCAGGC[A/G]AAGCCAACGACAGGT | 90293 |
rs370046783 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957421 | CAAATTATTCACAAT[A/T]AATGTTTGTTTAATG | 90293 |
rs370113261 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078518 | TAATATATTTAGCCT[C/T]AATGAGTCTGACCTC | 90293 |
rs370118598 | snp | A/G | 0.000555846 | 0.0166618 | synonymous-codon, intron-variant | KLHL13 | GRCh38.p7 | X:117983515 | TATATCCTTGAAATC[A/G]GCTTGTTTTAATGAC | 90293 |
rs370190141 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991088 | TAACCACTATCTCCA[A/G]TGTGTTTTTGGGGTA | 90293 |
rs370212566 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007337 | TCACTTGAGCCACTG[A/C]ACTCCAGCCTGGGCA | 90293 |
rs370229144 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118090775 | CAGCCATCCCATTAC[C/T]GGGTATATACCCAAA | 90293 |
rs370269323 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967432 | CTCCCCAAGTTTGGC[-/C]ATACTTAAGTCTCAA | 90293 |
rs370277779 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059522 | GGGGGCTTACTAGGA[A/G]ATTTCACTCTATATC | 90293 |
rs370301100 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117947132 | TATTTATGATATATA[A/G]CACACACACACAATT | 90293 |
rs370328255 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118033550 | AATGCTGAGAGATTT[C/T]GTCACCACCAGGCCT | 90293 |
rs370344033 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024807 | TTTCAAAAAACGTTT[A/G]GTAGTTTCTACAAAT | 90293 |
rs370353515 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118106143 | ACCTCGTGATCCGCC[C/T]GCTTTGGCCTCCCAA | 90293 |
rs370353811 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970642 | CTGATGAGAAAAACA[C/T]GTTAAACATGATGTT | 90293 |
rs370367378 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057694 | AGTCGGGTGTGGTGG[C/T]GGACACCTGTAGTCC | 90293 |
rs370384139 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089624 | AGAGAAAGAAAGAGA[A/G]AGAAAGAAAGAAAGA | 90293 |
rs370563132 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117937684 | TATAATTTTTCTACT[G/T]ATAAAAAGGATTATA | 90293 |
rs370567795 | in-del | -/A | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118431 | AGGTTAAAAAAAAAA[-/A]TAAGTACAAACTGAG | 90293 |
rs370608559 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117945812 | AATCAACTTAAAAGG[G/T]GGTTCAAAATTATAG | 90293 |
rs370619153 | snp | A/C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118043134 | AATAAATTGGAAAAT[A/C/T]GAGAATAAATTAATA | 90293 |
rs370623715 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092311 | TTTAAAGCAGTGAAA[A/G]AAACACCTTACCTAT | 90293 |
rs370684232 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045169 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 90293 |
rs370717557 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908395 | CTATCCCTCCCCTAG[-/C]CCCCCAACCCCAGAC | 90293 |
rs370749656 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117990186 | GCATACCTAAATGGC[G/T]CCTTTTGATGTTTGC | 90293 |
rs370751662 | snp | A/G | 0.0209675 | 0.10022 | intron-variant | KLHL13 | GRCh38.p7 | X:118033243 | GGAAATACAGAGAAC[A/G]CCACAAAGATACTCC | 90293 |
rs370781101 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070714 | CTCCAATTGGTAGAT[C/T]TGTCATTTTCTTTTT | 90293 |
rs370791252 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118055566 | AAACTGATGTAAAGT[A/G]AGTGAGGGTCTCACC | 90293 |
rs370808957 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901197 | GCATATTGGAAGCAC[A/G]TTTTATGCATAGGAG | 90293 |
rs370839342 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015204 | CCCTTAACCACACTA[C/T]TATAACTAGATCATA | 90293 |
rs370852440 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092873 | GTGACAGGTACCCAG[A/G]ACCTCTCTGTACTAT | 90293 |
rs370871756 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117992182 | TCAAGGAAGTTAGCA[G/T]CATGGGGTGCCTTGA | 90293 |
rs370878038 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117920673 | TTTGAAAAATAATTA[C/T]AATGTGCACTTCTAC | 90293 |
rs370903640 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036909 | CAAGAAAAAAACAAA[C/G]AACCCCATCAAAAAG | 90293 |
rs370912095 | snp | C/T | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:118009327 | TGAAGTCCTTGCCCA[C/T]GCCTATGTCCTGAAT | 90293 |
rs370946126 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118054804 | ATTAAAAAGACAAAG[C/T]ATTTCCCTCTAAATA | 90293 |
rs371006810 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109221 | GAACTCAACACATGT[C/T]TAGATTTAGACCATT | 90293 |
rs371109643 | snp | C/T | 0.000672425 | 0.0183238 | intron-variant | KLHL13 | GRCh38.p7 | X:117919734 | TTAAATAAAAAGACA[C/T]TCAATTAAATGAAGG | 90293 |
rs371143536 | snp | G/T | 0.0787474 | 0.182133 | intron-variant | KLHL13 | GRCh38.p7 | X:118019489 | TGTGCAGAAGCTCTT[G/T]AGTTGAATTAGATCC | 90293 |
rs371145116 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910236 | GGATTCTTATCTAAA[G/T]GTATCAATGATCTAC | 90293 |
rs371152724 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117937412 | AATTTCAGGTTACTT[G/T]CACATCACTGTTCTT | 90293 |
rs371152759 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045648 | TGTCTACTAAAAGTA[C/T]ACACAAAAAAAGTAG | 90293 |
rs371157183 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099409 | GTCCTAAAAAGTAAG[C/T]ATTAATATGTGTCTG | 90293 |
rs371163420 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118013096 | GGTTGTAGGTGCTGC[A/G]ATTAAAGCAGTAAAC | 90293 |
rs371204407 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118105654 | CAAGACTGTAACCTA[C/T]TTCAGGGCAGTGAAT | 90293 |
rs371219001 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916189 | CAAACAAAAAAAAAA[-/A]CACTAGCTAATGGGC | 90293 |
rs371227704 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118049004 | AGCACCTATCTTAGA[A/T]AATATTTCAAATAAA | 90293 |
rs371233740 | snp | A/G | 0.0157677 | 0.0873799 | intron-variant | KLHL13 | GRCh38.p7 | X:117964304 | AAATTTTTCTTCTGA[A/G]GTGTTTCCATTGCCC | 90293 |
rs371244498 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118017956 | GCAATCAGAAAATAC[C/T]GCCACAACAACAAAC | 90293 |
rs371256154 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117964264 | TTATCTACCTCCAGT[A/T]CAAGTCTCCTCATTT | 90293 |
rs371261116 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117964998 | ATCATTGATGGACAT[C/T]TGGGTTGGTTTCAAG | 90293 |
rs371274814 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050327 | TTTTTGCCAATATTG[A/T]AAGTATTATCCTTGT | 90293 |
rs371308162 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903973 | AATTTGAATACTTAT[C/T]CACTTTTTATTATTA | 90293 |
rs371353443 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078458 | CTAACTTGTTTTCTG[C/T]CCCTATAATTTTGCC | 90293 |
rs371361097 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998489 | GATTCTAAAAAAAAA[A/C]ACAAGAATCAAAGAA | 90293 |
rs371413413 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118072175 | CTCAGAAATAACGCC[A/G]CATATCTACAACTAT | 90293 |
rs371419245 | in-del | -/TTATCTTTTATTT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027520 | AGTTGTTTTTTATTT[-/TTATCTTTTATTT]CCATTTTTTCCATGA | 90293 |
rs371438780 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010229 | ATTTGACCCAGCCAT[C/G]CCATTACTGGGTATA | 90293 |
rs371444996 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955682 | GCTCATCACAGATAC[A/G]TGGCTCAATGGAAGC | 90293 |
rs371451183 | in-del | -/TGT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117976986 | TAACTTGCCCAATGT[-/TGT]ATCACAAGCTAGCAG | 90293 |
rs371503719 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057676 | ATACAAGAAAAAAAA[-/A]TTAGTCGGGTGTGGT | 90293 |
rs371517833 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921859 | CTCCCTCTAGGGAAA[A/G]AGATGAATATTTTTA | 90293 |
rs371548241 | snp | A/C/T | 4.57491e-05 | 0.00478255 | missense | KLHL13 | GRCh38.p7 | X:117909879 | TCCAGGCGAAGCCAA[A/C/T]GACAGGTAGCCTTAA | 90293 |
rs371554659 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118095100 | CACAGACTGGCAAAT[C/T]GGATAAAGAGTCAAG | 90293 |
rs371586670 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963401 | CACACAAACAGTAAA[-/A]TTATTCCCTGTCCAA | 90293 |
rs371614342 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037221 | ACTAGAAATACCATT[C/T]GACCCAGCCATCCCA | 90293 |
rs371672344 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939481 | TTGTGGGTCAAATGG[A/T]ATTTCTGGTTCTAGA | 90293 |
rs371678514 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118012698 | GGGGGCAGGGGGCGG[A/G]GGTATTCTGTCTACT | 90293 |
rs371718391 | snp | A/G | | | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898428 | GGAGGTAGCTCATGC[A/G]AGTTGGCAACCTTTT | 90293 |
rs371728586 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107000 | CTTCCCAATGGCTTA[A/C]CTATTACAAATGCTT | 90293 |
rs371729574 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942333 | GAGAGTTCTGTAGAT[G/T]TCTATTAGGTCTGCT | 90293 |
rs371745710 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036216 | TCAAGCTACCAATGA[C/T]TTTCTTCACAGAATT | 90293 |
rs371821504 | in-del | -/TTGAACAAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013115 | AAAGCAGTAAACAAG[-/TTGAACAAG]ATGCCTGGCCTCTTG | 90293 |
rs371849697 | snp | A/G | 8.43621e-05 | 0.00649415 | intron-variant | KLHL13 | GRCh38.p7 | X:117909293 | ATGCTTAATATAAAT[A/G]CACTTACGCAGTTCA | 90293 |
rs371854649 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118065870 | ACATCGCTATTTTAA[C/T]AGATACTAAAATTCT | 90293 |
rs371856750 | snp | C/T | 0.000117606 | 0.00766739 | synonymous-codon, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117945557 | TTTCATGTGTTGGTC[C/T]TCCTCTTCCACGAGA | 90293 |
rs371871106 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030715 | GTTCATCTTCCTCTT[C/G/T]TGTGTTCTCTCTCTC | 90293 |
rs371877391 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010277 | ATCATGCTGCTATAA[A/G]GACACATGCACACGT | 90293 |
rs371886839 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957617 | TTTAATTTAAATATA[A/T]TATCAGCTAAACCTT | 90293 |
rs371926469 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117976251 | ATTATTAAGTCACTT[A/T]TAATTACCTCTCATG | 90293 |
rs371941388 | in-del | -/TATATTAATATT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117989419 | TATTGTATTAATATT[-/TATATTAATATT]CATTTTAAGGAAAAA | 90293 |
rs371951322 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094009 | CTCCTCACCAGCAAC[A/G]GAACAAAGCTGGACA | 90293 |
rs371957961 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117980681 | ATTTTCTATGAGAAA[A/G]AGCCATTTATATTCA | 90293 |
rs371970376 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052673 | CTACTAAAAAAAAAA[-/A]CAAAATACAAAAAAT | 90293 |
rs372011886 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010045 | CCACTATGAGATACC[A/T]TCTCACACCAGTTAG | 90293 |
rs372078427 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107375 | TCTACTCACCATTTA[A/C]GAGATGCACATTCGA | 90293 |
rs372088369 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050850 | TCAGTGGTCTCCAAA[C/T]TTGAGCATACATCAG | 90293 |
rs372124801 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906026 | ATTAAATTGTTAAAT[A/G]ACTTTCCCATCAATC | 90293 |
rs372126001 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928813 | TTATCCCAAATTAGG[A/C]AGGAGAATTGCAATA | 90293 |
rs372132372 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117997079 | GGGAAGACTCATACT[C/T]ACTTGCACTTTGCAA | 90293 |
rs372132828 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108704 | CAAATCAGTGAGACA[G/T]GCAAGTGTGCACAGA | 90293 |
rs372141002 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118019542 | TTGCCATTGCTTTTG[A/G]TGTTTTAGACATGAA | 90293 |
rs372142256 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118018741 | AGACATTTTTGTTAC[A/G]GCTATTATAAATTGA | 90293 |
rs372152324 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036324 | AAGCTGGAGGCATCA[C/T]GCTACCTGACTTCAA | 90293 |
rs372208779 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | KLHL13 | GRCh38.p7 | X:117965414 | TCTGTTAATATCCTT[C/T]GCCCACTTGTTGATG | 90293 |
rs372224123 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971658 | GGAATTGCTTCTTTT[C/G]GACTGAGAGCATAAC | 90293 |
rs372225154 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118052310 | GAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 90293 |
rs372273839 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041940 | TTTCAAAAACAAGAC[A/C]CAAAGATCTGTTGCC | 90293 |
rs372282077 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118095937 | CAAAGCAGTGTGTAG[A/G]GGGAAATTTATAGCA | 90293 |
rs372386389 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117993972 | AACTCCCGACCTCAG[A/G]TGATCCACCCACCTC | 90293 |
rs372395225 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029747 | GCCAAGGCGAGCAGA[C/T]TGCTTCAGTCCAGGA | 90293 |
rs372400179 | snp | A/G | 9.15206e-05 | 0.00676402 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909515 | ATTTCCAATGACGGC[A/G]ATGCCATGCTGGTAC | 90293 |
rs372411240 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938776 | CTTCTTCCTCACATA[C/T]TTTTCCTATCTGTTT | 90293 |
rs372421671 | snp | A/G | 2.32986e-05 | 0.00341303 | intron-variant | KLHL13 | GRCh38.p7 | X:117945418 | TAAACACTACCAAAG[A/G]GACAGCTTAAATTAC | 90293 |
rs372436229 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117934884 | AAGCATAAAAAAAAA[-/A]GATATTCAACATGAT | 90293 |
rs372445302 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082212 | CACAGTGGCTGTACT[A/G]ATTCACAACTCCACC | 90293 |
rs372492144 | in-del | CAATAAAACTCAAAA/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117987839 | TTGAGTGAAAAAACT[CAATAAAACTCAAAA/G]ACCAGTTGCCTTTCC | 90293 |
rs372526868 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074677 | CCCATAATTATTATC[C/T]ACATTTGAAAACTGG | 90293 |
rs372536861 | snp | A/C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117995034 | GCCTGGGCAATAGAG[A/C/T]GAGACTCTGTCTCTA | 90293 |
rs372569434 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117965898 | TAGGTATTGATGGGA[C/T]GTATCTCAAAATAAT | 90293 |
rs372699150 | in-del | -/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038934 | GGGAAAAAGATGATT[-/TT]GTCTTGCAACTTGCA | 90293 |
rs372699696 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926549 | AGTGGAAACCTTACA[A/G]GGCTGGGGTTTTAAG | 90293 |
rs372710113 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117990256 | AGTAGGTATATAATA[A/G]CTTTATGATAGAAGA | 90293 |
rs372714795 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118033289 | CTAAGACACATAATT[A/G]TCACATTCACCAAAG | 90293 |
rs372716668 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930286 | AGGAAGGAAGGAAGG[A/C]AGGAAGGCAGGCAGG | 90293 |
rs372727165 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117960230 | TCTCTACAAAAAAAA[A/C]GTAAAAATAATAAAT | 90293 |
rs372745087 | snp | C/T | 4.90599e-05 | 0.00495253 | missense | KLHL13 | GRCh38.p7 | X:117910047 | TCCACTTCGGTTAGA[C/T]TGTAGGTGTTGGCAA | 90293 |
rs372818229 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118071055 | AATGATGATTTCCAA[C/T]TTCATCCATGTCCCT | 90293 |
rs372870140 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087201 | TTACACAATGCTTAA[C/T]TTCCCTCTAAACTCT | 90293 |
rs372885384 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117992607 | TGGGCTTTTTTTTTT[-/T]CCTTTTTTTCTGTCA | 90293 |
rs372911235 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004877 | AATTCCTGCTGAAGA[A/G]GCAAAACCTCAATAA | 90293 |
rs372921524 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088361 | TAAGCATTATATATA[A/C]TACATTACTGAATTC | 90293 |
rs372977988 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117991129 | GGCTGGAAATTTTCA[A/T]TAAAAAGTAAAAAAA | 90293 |
rs373043370 | in-del | -/A | 0.00281987 | 0.0374431 | intron-variant | KLHL13 | GRCh38.p7 | X:117901951 | TCTACTGTGGCTGTT[-/A]AAAAAAAAAAAGAAA | 90293 |
rs373073875 | snp | A/G | 0.0240739 | 0.107039 | intron-variant | KLHL13 | GRCh38.p7 | X:118089670 | AAAGAAAGAAAGAAA[A/G]AAGAAAGTTTCAATG | 90293 |
rs373075474 | snp | C/T | 0.000189982 | 0.00974449 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972839 | GGCATGTTGTCACCA[C/T]GGTACTACAATAACA | 90293 |
rs373115796 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118052908 | AAATCTTTCTAAGGG[C/T]TGACACAAAACTTAG | 90293 |
rs373116325 | snp | C/T | 0.00015824 | 0.00889354 | missense, intron-variant | KLHL13 | GRCh38.p7 | X:118028430 | TAAATATACCGGTTA[C/T]GAAGTATTGCAGCAA | 90293 |
rs373163807 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906818 | AATCTATAGATCATT[G/T]CAAATGGAATAAAAT | 90293 |
rs373164256 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117966354 | ATCCAACTTACAAGG[A/G]ATGTGAAGGACCTCT | 90293 |
rs373206040 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118068277 | GGTAGAGAGGAAGAT[A/G]GCCGACTAGAAGCCC | 90293 |
rs373210032 | snp | C/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986203 | TTCTACAGCAGCAGA[C/G]GAATAACAAAAATTC | 90293 |
rs373222217 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010318 | CGGCATTATTCACAA[A/T]AGCAAAGACTTGGAA | 90293 |
rs373236702 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118096260 | GTATCACCACCGATC[C/T]CACAGAAATACAAAC | 90293 |
rs373249947 | in-del | -/CTTCTT | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117949 | TTTTTTCTTCTTCTT[-/CTTCTT]AAGGAAGTGATGCGG | 90293 |
rs373262456 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002181 | CCGGGTTAGATGCAC[A/G/T]AAATAGATGGCTAGA | 90293 |
rs373276866 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944664 | ATTAAGGGTAGTAAG[A/T]GGACCAATATAATTT | 90293 |
rs373291542 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943292 | CCTTGCTGAATCTGA[C/T]GATTATGTGTTTTGG | 90293 |
rs373294079 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118048780 | ACTTTCCCCTGGCCA[G/T]GACACCCTCATGAAT | 90293 |
rs373315367 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117967076 | GGATCTAATTAAACT[A/C]AAGAGCTTCTGCACA | 90293 |
rs373317414 | snp | C/T | 0.000555846 | 0.0166618 | intron-variant, missense, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973358 | TCTTCTTTTGAGCTG[C/T]AACAATACAAATGGG | 90293 |
rs373368601 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118099105 | TCTAAAACTTAAAGT[A/G]TAATAATAATAAAAT | 90293 |
rs373393143 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117932305 | CCTAACTGTAGCTTT[A/G]TACTCATTGACCAAT | 90293 |
rs373415017 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036653 | CCCTAGAAGAAAACA[C/T]AGGCATTACCATTCA | 90293 |
rs373457252 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118053432 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 90293 |
rs373460157 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117962260 | CATTTTAGGCCATTC[A/G]TTTGCAGTAATTTGA | 90293 |
rs373466331 | snp | G/T | | | missense | KLHL13 | GRCh38.p7 | X:117899081 | CTACCATACAACGAT[G/T]ATTCCAAGAATACCC | 90293 |
rs373472302 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987274 | TCACCCAAAGATCCA[C/T]ATAATAAACAAAAGG | 90293 |
rs373489781 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117929759 | CTAGCCTGGGCAATA[C/T]AGTGAGACATCGTCT | 90293 |
rs373524431 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117962324 | TTGGGTTTTTTTTTT[-/T]CATTGAGTATTTGCA | 90293 |
rs373550507 | in-del | -/AAGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903193 | CGAGAGAGAGAGAGA[-/AAGA]GAGAGAGAGAGACTA | 90293 |
rs373625143 | snp | A/G | 0.000114088 | 0.00755187 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899130 | ATTTTCGAAGACAGC[A/G]ACCCCAACATCACTC | 90293 |
rs373634166 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050440 | AGTATCAAATGCCAG[G/T]CTTAGGCTTAGCTGT | 90293 |
rs373652022 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117999875 | TATAGCCCAGTTAGG[A/T]CAAATAATTGTTTTA | 90293 |
rs373709269 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056076 | ACGTAGAAAATCCTA[A/C]AGAATTGATGGAAGA | 90293 |
rs373772163 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117931234 | CACAAAAAGAGCAGT[C/T]CAATAGGCACCAATC | 90293 |
rs373798151 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118023271 | TTAAGGAACAACTCT[C/T]ACATATTACCATTAA | 90293 |
rs373801642 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081083 | TATGGACATAAATAT[C/T]GAAACAATAGACACT | 90293 |
rs373823312 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017990 | TGACTCTCACCACAA[C/T]GTGTCCTCCTAGACA | 90293 |
rs373825330 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052792 | AGATCGTACCACTGC[A/G]CGCCAGTCAGGCCGA | 90293 |
rs373833907 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117904396 | ACCAACAACTCTGAT[A/G]GGAAGAGGGAGTAAG | 90293 |
rs373838556 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109498 | TCTATGAATATTGCG[C/T]TCTAAGGCAGAATGT | 90293 |
rs373851970 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118020993 | CTGGGGACTGTTGTG[A/G]GGTGGGGGGAGGGGG | 90293 |
rs373956882 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049475 | GATTTTTTTAAATGT[C/T]CCAGAGTGTTAGATC | 90293 |
rs373957206 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117964683 | TGTTGGTGTGCTGCA[A/C]CCATTAACTCGTCAT | 90293 |
rs373960044 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118032464 | CCTAACTGGGAGGCA[A/C]CCCCCAGCAGGGGCA | 90293 |
rs373996572 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085955 | ATGGATTTTTTTTTT[-/T]GAGACGGAGTTTTGC | 90293 |
rs374002615 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010066 | CACCAGTTAGAATGG[C/T]AATCATTAAAAAGTC | 90293 |
rs374017495 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118094350 | AGAGAAAAAAGAGTA[C/T]AAAGAAATGAACAAA | 90293 |
rs374017691 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117102 | ACATGGATTCTAGTG[C/T]CGGGAGGCAGAAAAA | 90293 |
rs374054694 | in-del | -/CTT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100138 | CTGCTTATTGTTCTT[-/CTT]ATTTTTGCCAAAATA | 90293 |
rs374061985 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024999 | CAACAGGAAAATAGA[C/T]AGAATAAATTGTTGC | 90293 |
rs374069326 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971734 | ATAATTGTGCATCTC[C/T]ACCTCACATAAAACA | 90293 |
rs374118886 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118106067 | CCACCACGCCCAGCT[-/AT]TTTTTTTTTTTTTTT | 90293 |
rs374209955 | snp | G/T | 0.0826288 | 0.185706 | intron-variant | KLHL13 | GRCh38.p7 | X:118019494 | AGAAGCTCTTTAGTT[G/T]AATTAGATCCCATTT | 90293 |
rs374215283 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944706 | GAAGACATTAATGGA[C/T]ATCCAGTACCATATT | 90293 |
rs374272604 | in-del | -/ACA | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973304 | GAAAATGAAACAACA[-/ACA]TACCTACTCAGAATA | 90293 |
rs374289549 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085819 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGTGTGTGT]ATCATATATTCTTCA | 90293 |
rs374305528 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117934031 | AAGCAAATTAAGGCA[A/G]AAACAGAAACTAAAA | 90293 |
rs374310655 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118055111 | GGAGTACAGCATGCA[A/G]GTCTGAATAAAGGTA | 90293 |
rs374314248 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118054837 | TGAAATACTGTTTAA[C/T]ATCCTATTCGATCAA | 90293 |
rs374338614 | snp | A/G | 2.28029e-05 | 0.00337653 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117920296 | GACTCTATGCACAGG[A/G]AAAGCATCATCTGTG | 90293 |
rs374352125 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117953336 | GCATGTTCTCACTCA[C/T]AGATGGGAATTGAAC | 90293 |
rs374417827 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911340 | CATAAAATGACAGCC[C/T]AGTTAGGATATAATA | 90293 |
rs374430602 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118110501 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAT | 90293 |
rs374434362 | snp | C/T | 2.49909e-05 | 0.00353481 | intron-variant | KLHL13 | GRCh38.p7 | X:117901783 | ATGGAAAGATAACCA[C/T]ATAGTTAAAAGCTTA | 90293 |
rs374436741 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117992823 | GTTATTTATTCTTAG[G/T]TGTGTTCAACTTAGC | 90293 |
rs374447757 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921654 | ACTTCAAATAAAACT[-/AT]GTTTTGTTTCACAGA | 90293 |
rs374476582 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118071370 | TAGTTTACAGTCCCA[C/T]CAACAGTGTAAAAGT | 90293 |
rs374524681 | snp | A/C | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118336 | ATTGGGTAGAAAGCA[A/C]CTTGTACAGAAGTTT | 90293 |
rs374571054 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901290 | AATTAATTGTTGCTA[C/T]AGAAACTATGAATGG | 90293 |
rs374587156 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059827 | AGAGACATTATATTA[C/T]AATGGTTAAGAGCAT | 90293 |
rs374594973 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118072682 | GAAGGACATGAACAG[A/T]TTTGTCATTTTCTTA | 90293 |
rs374606469 | snp | C/G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118003599 | TAATAAACCAGTAAA[C/G/T]AAATTAATATTAATC | 90293 |
rs374638973 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118006426 | TCTTGGCCCTTTACC[C/T]TGCTACATGAACTTG | 90293 |
rs374644023 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900069 | GAATGCTGAATATAC[A/G]TGGAATTTTATACAT | 90293 |
rs374649744 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002220 | TGTCATTTTCCTCAC[A/G]GACTTCATGGTTTGG | 90293 |
rs374685849 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117908664 | TTATGACCAATTTTA[C/T]ACTGGGAAGACAAAA | 90293 |
rs374701042 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959648 | TTAATATCACATTCT[C/T]TTTCAAGGTAAATGG | 90293 |
rs374703968 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015704 | GTATGAAAACATGCA[A/T]CTCTTCAGTTATAGG | 90293 |
rs374746994 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118105603 | ATATTAGTATTGGCC[A/G]ATATCAAATTGACTC | 90293 |
rs374747697 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901573 | ACAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 90293 |
rs374760388 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038136 | GAAAAGATTACATCT[A/C]GATTTAGATTGGAAC | 90293 |
rs374772614 | in-del | -/ATAAAAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117984331 | TTGATGAGCTCTAAT[-/ATAAAAT]TTCATTTATTTCCAT | 90293 |
rs374890835 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996473 | AAAGAGCATAGAACC[A/G]ATTCCAATTTGCAAT | 90293 |
rs375089549 | in-del | -/AAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083511 | TATGATTCCACTCAT[-/AAT]GAGGAATTTTTTAAG | 90293 |
rs375100801 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118096018 | ATCACAATTAAAAGA[A/T]CTAGAAAAGCAAGAG | 90293 |
rs375111280 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118042912 | CAGAAATAAATGACA[C/T]TGAAATGAAAAAAAA | 90293 |
rs375112126 | in-del | -/CAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080411 | TATAAGTAACTTAAA[-/CAAA]TCAACCAGCAAGAAA | 90293 |
rs375139093 | snp | A/G | 0.000189982 | 0.00974449 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909341 | ACCAACTGCATACAG[A/G]TATCCTTTGAGGGCA | 90293 |
rs375153953 | snp | A/G | 0.000189982 | 0.00974449 | intron-variant | KLHL13 | GRCh38.p7 | X:117945592 | TGAAAGTTTTTTTAC[A/G]TAAGAAAGAAGGGGA | 90293 |
rs375163816 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099910 | GAAGGAAGGAAAGAA[A/G]GAAGGAAGAAAGGAA | 90293 |
rs375209732 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051986 | AGTAACTATTACAGT[C/G]TGGTACTAGTGTGGG | 90293 |
rs375243513 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045209 | AAACCCTGTCTCTAC[C/T]AAAAATACAAAAAAA | 90293 |
rs375255247 | snp | A/T | 0.0194105 | 0.0965841 | intron-variant | KLHL13 | GRCh38.p7 | X:118076056 | CAGTTTCTAATTTTA[A/T]GTTTATTTGAGCACT | 90293 |
rs375272627 | snp | C/T | 0.000189982 | 0.00974449 | intron-variant, utr-variant-5-prime, splice-acceptor-variant | KLHL13 | GRCh38.p7 | X:117972844 | GTTGTCACCACGGTA[C/T]TACAATAACAGTAAA | 90293 |
rs375364196 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118095191 | AAATAAAGGGATGGA[A/G]GAAGATCTACCAAGC | 90293 |
rs375399908 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010253 | GGGTATATACCCAAA[G/T]GACTATAAATCATGC | 90293 |
rs375404014 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911587 | CTGGTGTGTGATGTT[A/C]CCCTCCCTGTGCCCA | 90293 |
rs375417506 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117984240 | AGTTTTAAAAATAGA[A/G]ACCACTACAGAAGCA | 90293 |
rs375419516 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117956013 | CTAAAATGTTTTAGG[G/T]TCCACCATTTTACTA | 90293 |
rs375427937 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118073022 | TTGCTTGAGCCCTGG[A/C]GGTCAAGGCTTCAGC | 90293 |
rs375436473 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118043635 | GAAGGAAGGACAAAA[A/C]CCTTATGATCATTTC | 90293 |
rs375443331 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117999986 | TAACTTCTTCTTTAA[C/G]ATTATTATTTTATAT | 90293 |
rs375443346 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108266 | TCACAATCCTCTATA[A/C]CCATGTCCTTACAAG | 90293 |
rs375450133 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036325 | AGCTGGAGGCATCAT[A/G]CTACCTGACTTCAAA | 90293 |
rs375454669 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030146 | GGGTTTTCATAATTC[C/T]AAAAAGCAAATAAAT | 90293 |
rs375487268 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118090839 | CACACGTATGTTTAT[A/T]GCGGCACTATTCACA | 90293 |
rs375546876 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080120 | CCTTTCACCATATAC[A/G]AAAATAACTCAAAAT | 90293 |
rs375570753 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963700 | CAGTGTAAAAGTGTT[C/T]CTATTTCTCCACATC | 90293 |
rs375707999 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026604 | AGCAGTTTACAAATG[A/G]ATAACTCATTTTAGA | 90293 |
rs375760555 | in-del | -/CTTCATATATTCC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023563 | AAAAGAGTTTATTCC[-/CTTCATATATTCC]ATTTTTCTTTTTTGA | 90293 |
rs375764021 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998865 | CAAAACCATATAAAT[G/T]CTATGTAAATTATAC | 90293 |
rs375766338 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080410 | TATAAGTAACTTAAA[-/A]CAAATCAACCAGCAA | 90293 |
rs375784041 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948590 | AAATAGTCCCATTTC[A/G]CCAGCCCTACAAGAT | 90293 |
rs375785754 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036915 | AAAAACAAACAACCC[C/T]ATCAAAAAGTGGGCA | 90293 |
rs375800371 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916178 | AACAAAACAAACAAA[A/C]AAAAAAAAAAACACT | 90293 |
rs375800888 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986767 | TATCTTACATGGTAA[C/T]TTGAGTCTATGGTTT | 90293 |
rs375814989 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118009998 | GAAAAAATGCTCATC[A/T]TCACTGGCCATCAGA | 90293 |
rs375841484 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950029 | GAATTAGAGAAAAGC[G/T]AGAAAGGTAAAAGTA | 90293 |
rs375863899 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117905740 | GATGCAGGTATGCAA[G/T]GTATAATAATCACAT | 90293 |
rs375919396 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024341 | ACCTCAAATTTGGAA[A/G]AGCAAAGATTTCTTG | 90293 |
rs375924219 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117947151 | ACACACACAATTTTA[A/G]ACAACTTTTGTGGAC | 90293 |
rs375926902 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036624 | CTTAAATGTTAGACC[C/T]AAAACCATAAAAACC | 90293 |
rs375930851 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911470 | TTGTTACATAGGTAT[A/T]ACACGTACCATGGTG | 90293 |
rs375933707 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083589 | GGGCGAGAGTGGGGG[A/G]CAGGTAATGAAGAGA | 90293 |
rs375967011 | in-del | -/CTCTCTCTCT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991847 | TCTCCTACAGTGAAA[-/CTCTCTCTCT]CTCTCTCTCTCTCTC | 90293 |
rs375993032 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971509 | GCCTATTTTTTTTTT[-/T]ACTTCATAAAGTTTA | 90293 |
rs376032375 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036706 | TTCATGTCTAAAACA[A/C]CAAAAGCAATGGCAA | 90293 |
rs376046169 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108932 | CTGCCTAAACCTCTC[A/G]AGTAGCTGAGACTAT | 90293 |
rs376054802 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118019924 | TTTGAAGTCAGGTAG[C/T]GTGATGCCTCCAGCT | 90293 |
rs376067789 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089622 | AGAGAGAAAGAAAGA[A/G]AAAGAAAGAAAGAAA | 90293 |
rs376074224 | snp | A/G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117947028 | ATTTAATAAAGAAGA[A/G/T]AATAACTTAAGATTT | 90293 |
rs376079320 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117990302 | TGAATGGATCAATAG[A/G]TGACTGCTGAACTGA | 90293 |
rs376083974 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118033481 | CAGAATTTCATATCC[A/G]GCCAAACTAAGCTTC | 90293 |
rs376088361 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118008459 | CTACTAGTATTGGAA[C/T]TTTAATATCTACTAC | 90293 |
rs376093791 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036764 | TAATTCAACTAAAGA[A/G]CTTCTGCACAGCAAA | 90293 |
rs376128295 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099969 | AGACACCCTTGACTA[C/T]ACAAATGAGCTATAC | 90293 |
rs376155537 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118032703 | CCTCCTCCAAAGGAA[C/T]GCAGTTCCTCACCAG | 90293 |
rs376160149 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930035 | CCTCAAACCTACAGA[C/T]AACATCATACTTAAT | 90293 |
rs376197450 | snp | C/T | 0.0152462 | 0.0859689 | intron-variant | KLHL13 | GRCh38.p7 | X:117938151 | TCACATTTTCCCTGT[C/T]ACTTTTTTTTAGTAT | 90293 |
rs376197480 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118046262 | TGGAACTGGAGGACA[C/T]TGTGTTAAGTGAAAT | 90293 |
rs376213402 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994737 | GCAAAAGTCACATCT[C/T]GTTCAACTTTCATAA | 90293 |
rs376231799 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014654 | GTGGATATCACAGAA[A/C]CTGACGATATGTGAC | 90293 |
rs376288542 | in-del | -/GGAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099902 | GAAGGAAAGAAGGAA[-/GGAA]AGAAGGAAGGAAGAA | 90293 |
rs376302516 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089801 | AGTATCAATAGGGCT[C/G]GGTGTGGTGGCTCAC | 90293 |
rs376315112 | snp | A/G | 0.000189982 | 0.00974449 | missense | KLHL13 | GRCh38.p7 | X:117920324 | GTGTCACCTGGCATC[A/G]GGGTCACATCACAAA | 90293 |
rs376348565 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010301 | CACACGTATGTTTAT[A/T]GCGGCATTATTCACA | 90293 |
rs376372512 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118110336 | GAATCATGTCTCATT[C/T]GTTTTCTACCTTTCT | 90293 |
rs376375160 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030830 | TGAACGTCCTAGCCT[C/G]CAGAACTGTGAGAAA | 90293 |
rs376411736 | snp | C/G | 0.000114511 | 0.00756586 | missense | KLHL13 | GRCh38.p7 | X:117919668 | CCTTAGACCGACTTT[C/G]CTCACACCATGAAGT | 90293 |
rs376422344 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118003718 | AGGAACTACAACAAT[A/G]GAAAGTAAATATCCA | 90293 |
rs376450912 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118054090 | AAAAACTGCTGAGCA[C/T]TTTATAGGGAAAACT | 90293 |
rs376468250 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118021238 | GTAAATGGCATTATC[A/T]CCTTTTTTTTTATTA | 90293 |
rs376608896 | snp | A/C | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:118097136 | AAAAGAGGAAGTCAA[A/C]TTGTCCCTGTTTGCA | 90293 |
rs376614930 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118010675 | CAGCGCACCAGCATG[G/T]CACATGTATACATAT | 90293 |
rs376641874 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117964274 | CCAGTTCAAGTCTCC[A/T]CATTTAGTCCAGACA | 90293 |
rs376670572 | in-del | -/CAAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117978916 | GTAGTGGAAATCAAT[-/CAAT]GGTTTTTATTTTATT | 90293 |
rs376685284 | in-del | -/TCCTTATT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981597 | CATTCATTCCTTATT[-/TCCTTATT]CAGCTTGATTTAAGT | 90293 |
rs376716803 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926956 | TGTCGCCCAGGCTGG[A/C]GTGCAGTGGCGCAAT | 90293 |
rs376720502 | snp | A/G | 0.0183711 | 0.0940641 | intron-variant | KLHL13 | GRCh38.p7 | X:118009572 | TTGTAGGTATGCGGC[A/G]TTATTTCTGAGGGCT | 90293 |
rs376730818 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053505 | TGGGGTGGGGCGAGG[G/T]GGGAGGGATAGCATT | 90293 |
rs376748830 | snp | G/T | 2.30065e-05 | 0.00339157 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117945515 | CAAATGGGATGAGAG[G/T]CCCATTTCGCTGCCT | 90293 |
rs376757655 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051262 | AATAAAATTTATGGC[C/T]GGGTACGGTGGCTCA | 90293 |
rs376777451 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056347 | TACCATGTTCATGGA[C/T]TGGAAGCCTTAATAT | 90293 |
rs376795223 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118042930 | AAATGAAAAAAAAAA[-/A]TACAAAAGATCAACA | 90293 |
rs376815954 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939122 | AAGGCCCTGGTGTGT[G/T]ACGTTCTCCTCCCTG | 90293 |
rs376830373 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117966065 | GCCAGGGCAATCAGG[C/T]AGGAGAAGGAAATAA | 90293 |
rs376831811 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117996873 | ATGCTCACATATTAT[C/T]TGCCAAAGAAACAGG | 90293 |
rs376836480 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906056 | CCCCTCTTCCTGCCA[C/G]CCATTCCCATCACCT | 90293 |
rs376838952 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017151 | CTTCAGTAGATCTCT[A/G]CAGTCTGTGAAGTAT | 90293 |
rs376840190 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923377 | GATGAGTCTAGGTAC[C/T]GTATGCCCCCTTTAT | 90293 |
rs376843018 | in-del | -/ATAAAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994905 | TATAAAAAATAAAAA[-/ATAAAAA]TAGCAAGGAGTAGTG | 90293 |
rs376855524 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088596 | GATAACTTTAAATAA[C/T]TCTATTGACAAAGCA | 90293 |
rs376860774 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066129 | TTAAGCCAGTATGCT[A/T]TTTAAATTATCTGGA | 90293 |
rs376866029 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117983822 | TAAGCATAACAATGA[C/T]TGGCAGTTGATCTAA | 90293 |
rs376871686 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031660 | ATATATATTTAGTTA[C/T]ATATAATATATATAA | 90293 |
rs376914623 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108426 | ATTTACTTTCACCCC[-/C]TTTCTTCACTTGCCT | 90293 |
rs376980452 | snp | G/T | 0.000437234 | 0.0147792 | missense | KLHL13 | GRCh38.p7 | X:117909967 | GCTCAAAAGGGAGTT[G/T]CAAGAACTCCCCTGT | 90293 |
rs376982564 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996167 | GTGTGTCTCTACACA[A/T]CTGACATACAAGGAA | 90293 |
rs377021530 | in-del | -/AATT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901996 | AACTTCAAATTTAGC[-/AATT]AATTATTTTTCTCTT | 90293 |
rs377050599 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023432 | TAAAAGGAGCATGTA[A/G]TTGTTTTCAAACACC | 90293 |
rs377074897 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118110620 | CTAACCTTATCATCC[A/G]CCCGCCTCGGCCTCC | 90293 |
rs377135438 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117977083 | TTCTTCCCAATGAGA[C/G]CATTCCACAAGATGC | 90293 |
rs377144272 | snp | G/T | 0.000779119 | 0.0197219 | missense | KLHL13 | GRCh38.p7 | X:117945495 | GGTCCTGCCTTGGAA[G/T]ACTGCAAATGGGATG | 90293 |
rs377151140 | snp | A/G/T | 9.84624e-05 | 0.0070159 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898877 | CACATTGCAAAGATA[A/G/T]AACTACAGCATCTTA | 90293 |
rs377162760 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027682 | ACACACTTTCATACA[C/T]GCCCCACCTTTCACA | 90293 |
rs377177151 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093403 | ATGAGGAAACCATGA[C/T]GCAATAAAATGAAGT | 90293 |
rs377177650 | snp | A/C | 2.48133e-05 | 0.00352222 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117910064 | GTAGGTGTTGGCAAT[A/C]CGTCCAACTTCAACA | 90293 |
rs377180254 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052674 | CTACTAAAAAAAAAA[A/C]AAAATACAAAAAATT | 90293 |
rs377187019 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961087 | TATGCTTGCAAAATC[A/G]ATGTAATCAAAACAA | 90293 |
rs377195610 | snp | C/T | 4.56064e-05 | 0.00477505 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909773 | TCTCATGAAATCCAC[C/T]GTTTGCACGTAATTA | 90293 |
rs377264998 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014673 | ACGATATGTGACTTC[A/G]CCTCCAGCGGCCCAG | 90293 |
rs377291658 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900919 | AATGCATTAAAAAAA[G/T]AAAGAAATTCTACAG | 90293 |
rs377340227 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907538 | GATTTTCTAAGAAAC[A/C]ACCAAGTCACTACTT | 90293 |
rs377342346 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117966398 | CAAACCACTGCTCAA[G/T]GAAATAAAAGAGGAT | 90293 |
rs377351378 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117989490 | TCCAAAAAAAAAAAA[-/A]GTCTTCACATAAATG | 90293 |
rs377359475 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913162 | GGCCCAGAGAAATAC[A/C]TAATATTCTATTATG | 90293 |
rs377366742 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113212 | GAGGAACCGAATTAC[A/C]TGATTATTTAGCATA | 90293 |
rs377447886 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070506 | ACTTGTTTGATGGCC[C/T]AGTATATGGTCAATT | 90293 |
rs377453679 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108203 | TCTCCTTTTACTGAA[C/T]AGACTGTAAAAGCAC | 90293 |
rs377503929 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024586 | GCCAAAACACTTGAA[C/T]ATATGCTTCTAAAAT | 90293 |
rs377511749 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103960 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 90293 |
rs377561029 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118055003 | CCAGTCAGAACTCCT[C/T]AGAAAGCAGTATTTC | 90293 |
rs377708658 | snp | C/T | | | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899280 | GAGCCTTTCTCCCAC[C/T]GTACACATGCAATGC | 90293 |
rs377709443 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117962552 | ATGGAGTTAATCCCG[A/G]TATCATATGAGCAAG | 90293 |
rs377715432 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118012842 | GTTCCAGCCTCTAAA[C/G]AAGGTATATATACAA | 90293 |
rs377719920 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051547 | TTCATCTCAAAAAAA[-/A]GTAATAAATAAATAA | 90293 |
rs377764093 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118090920 | TAAGAAAATGTGGCA[C/T]ATATACACCATGGAA | 90293 |
rs377765911 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008489 | CAGACACCACAGAAA[C/T]AAGATCTAATACTAT | 90293 |
rs377766739 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036781 | TTCTGCACAGCAAAA[C/G]AAACTACCATCAGAG | 90293 |
rs386827166 | multinucleotide-polymorphism | AG/GA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117905238 | GTTATTTCATTATTT[AG/GA]AACCTTAACTTATTA | 90293 |
rs386827167 | multinucleotide-polymorphism | AC/GT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117919085 | CTGGAGTGCAATGGC[AC/GT]GATCTCAGTTCGCCA | 90293 |
rs386827168 | in-del | AT/GAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928722 | TTTATATCAGTCAAT[AT/GAC]TATATTAAAAAAGAA | 90293 |
rs386827169 | multinucleotide-polymorphism | ATT/GTC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117941867 | TAGTTATTTCTTGTC[ATT/GTC]TGCTAGCTTTTGAAT | 90293 |
rs386827170 | multinucleotide-polymorphism | AC/CT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963390 | TGTGCTATAAAGCAC[AC/CT]AAACAGTAAATTATT | 90293 |
rs386827171 | multinucleotide-polymorphism | CAC/TAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118006010 | ATGTGTCATTAAATA[CAC/TAT]GTTTAAGGCCATATA | 90293 |
rs386827172 | multinucleotide-polymorphism | AAG/GAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017408 | GAATAATTTGAAAGC[AAG/GAA]AAGGCAACATGGCTA | 90293 |
rs386827173 | multinucleotide-polymorphism | AA/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118019589 | ATGTTCTGAATGGTA[AA/TT]GCCTAGGTTTCCTTC | 90293 |
rs386827174 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023875 | TTTCCTATGTTTTAC[CA/TG]TATTTGGAATTTGAA | 90293 |
rs386827175 | multinucleotide-polymorphism | AAT/TCA | | | intron-variant, cds-indel | KLHL13 | GRCh38.p7 | X:118029672 | CGCAATTTAGTTTAT[AAT/TCA]TAAAGTTATGTTGGC | 90293 |
rs386827176 | multinucleotide-polymorphism | CAT/TAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066617 | ATGAAAAACATGATC[CAT/TAC]GAAAGAGAAACCTGA | 90293 |
rs386827177 | multinucleotide-polymorphism | GG/TA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073206 | ACATACCAGAGACTG[GG/TA]CAATTTACAAAATAA | 90293 |
rs386827178 | multinucleotide-polymorphism | ATA/TTC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103240 | AATATAAAGGTATGC[ATA/TTC]GATTTTTTATTCTAG | 90293 |
rs397808603 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959095 | ATCATTTAAAAAAAA[-/A]CACTCTAATTGTATC | 90293 |
rs397895309 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052537 | AAAAAAAAAAAAAAA[-/A]GTAGTAGAGGCCGGG | 90293 |
rs397895644 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052364 | TAAAAAAAAAAAAAA[-/A]TACAAAAAATTAGCC | 90293 |
rs397895992 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963266 | TTATGCTGGGAAAAA[-/A]TATTTTAGTATAATT | 90293 |
rs397896469 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117978808 | CTTTTTTTTTTTTTT[-/T]CTACCCGTGTATGCT | 90293 |
rs397976969 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118028394 | ATAGGAAAGACGTTA[-/A]TATAAGTTAAACTAT | 90293 |
rs527376733 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118109371 | GACTAAAAGAACAGA[A/C/T]TCGGGCAGTACAGCA | 90293 |
rs527840185 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118062314 | ATGACATGTTTTCTC[A/G]GCTTCAAGTATTTCC | 90293 |
rs527874515 | snp | C/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118008722 | AAGGAAAAAGACTGG[C/G]ATATGGCTAAATGCA | 90293 |
rs527969653 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066799 | ACAATGAAAGAAAAT[C/T]TAGTTTTTTTCCTTA | 90293 |
rs528104944 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914243 | GCTTTTTTTTTTTTT[C/T]TTCTGGCTAGCCGAG | 90293 |
rs528198553 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944151 | CCCGGGTATCACCAG[C/T]GGGGGCTCAGTTGGA | 90293 |
rs529315963 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078031 | TTACTCTTTCTGCAA[C/T]TGAATATCTGTGTAA | 90293 |
rs529375673 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118102520 | AAGAACAAAGAGAGT[C/G]CATATAATGCTGTGA | 90293 |
rs529410550 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025721 | GCACATCCTGCACAT[A/G]TATCCCAGAACTTAA | 90293 |
rs529601048 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117934231 | GAAGCCCAAACCTCA[G/T]CATCACACAGTATAC | 90293 |
rs529713066 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118031888 | AGTGGCTGCGTGCAC[C/T]GTGCGCGAGCCGAAG | 90293 |
rs530277396 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117903723 | TGGGAAGCTTTTAGA[A/G]GTAATTAAACCACAC | 90293 |
rs530387937 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117956876 | CAAAATCCAATCTTT[A/T]CATATGTCAAAGATA | 90293 |
rs530429045 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118004044 | CTGGAAGTCAGAGTC[A/G]GGGAGGCAAGGGTGT | 90293 |
rs530618798 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117904937 | TTGGTTATCTCACAT[A/G]TATCAGGAGTTCTTA | 90293 |
rs530823907 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118079548 | TATTTACAATAGTCA[C/T]AAAGAAAATGAAATA | 90293 |
rs531369170 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996787 | TACCACCAGTAGCAC[A/G]CACATAATACTTCAG | 90293 |
rs531374159 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957395 | CCTCCTTAACTAATT[A/G]CACAGTCCAGCAAAT | 90293 |
rs531607784 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115611 | TATCCCAAACCACTA[A/C]AGTCCTCTGACTACA | 90293 |
rs531702614 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036516 | CCTATTTAATAAATG[A/G]TGCTGGGAAAACTGG | 90293 |
rs531778283 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074838 | ATGTGCACATTGAAT[C/T]ATCCCTCCCGAAGTG | 90293 |
rs531833345 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117969448 | AAATGACAGAGTAAT[A/T]TATATGGTTTGCACC | 90293 |
rs531956479 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104455 | CCACTCATACTAGTG[C/G]GTTTAGCAGTTTTGT | 90293 |
rs532002073 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117947546 | GTAACAACTTATTTA[C/T]TTTGTCATTTGTCTC | 90293 |
rs532158823 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117993916 | TAATTTTGTATTTGT[A/G]GTAGAGACGGGGTTT | 90293 |
rs532164063 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040083 | ACAGTGACCAAAGAC[G/T]TAGATCACAACACCC | 90293 |
rs532612559 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073093 | GTGAGACACTCTCTC[-/A]AAAAAAAAAAAAACC | 90293 |
rs532644486 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118007464 | AGTTATATATTAGTA[C/T]TTTCAATAATGTGCC | 90293 |
rs532724675 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118114939 | CAGAAACTACTCTCA[C/T]CTCACTGCCATAAGA | 90293 |
rs532787008 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913355 | TTGGACTTATAATGC[A/C]ATTTACATATATAAT | 90293 |
rs533353823 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118107682 | AGTTGCCCAACAAAA[G/T]GCAGTCAGGATTTGA | 90293 |
rs533462774 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022731 | TAAGTTATGTTAAGA[C/T]ATTAACCCTCATCAC | 90293 |
rs533778960 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117905995 | TATGAAGTGATATAC[C/T]GGTACTAATCAACCT | 90293 |
rs533846213 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083198 | TATGGAGGTTCCTCA[A/G]AAAACTAAAAATAAA | 90293 |
rs533851947 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053023 | AGAAGAGGCATGGGG[G/T]TGTGAGATTGGAAGC | 90293 |
rs534005537 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928058 | AAACCTAGCATGACT[A/T]CAATACCAAACAAAA | 90293 |
rs534058092 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118043253 | TGTAATAAAGTGTCT[C/T]CAGCACAGGAAAGTA | 90293 |
rs534305992 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117961868 | GCTGACATTTTTATT[C/T]TAGCCCCGTGAGACC | 90293 |
rs534409976 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118058014 | GAGAAAGACAGGCAC[G/T]GGTACACGTTTTCTA | 90293 |
rs534413932 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005313 | GATTTGTGATAAATA[G/T]TTTTGAAAATAATTT | 90293 |
rs534594394 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069313 | ACCTTCCAGTGAGAT[A/C]AGATGTGTAAGTGGA | 90293 |
rs535441674 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037925 | TTGACTAAAAGATCA[C/T]GAATAGGTATTACAG | 90293 |
rs535500657 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118090003 | GAAGAATCGCTTGAA[A/C]CGGGGAGGCAGAGGT | 90293 |
rs535706954 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975641 | GGTGATCCACCCGAC[A/T]TGGCCTCCCAAAGTG | 90293 |
rs536191706 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118014604 | CCCTCCCCTTTTAGA[A/G]TCCCTAACAAAAACT | 90293 |
rs536674863 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117980272 | ACATACCAAATCTCA[A/G]AAGACATGCCAGTTA | 90293 |
rs536822905 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117925057 | TGAAACATCTAATGA[C/G]TTTGATAAATTTTAA | 90293 |
rs536937097 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024267 | ATTCACTTCTCTGGT[G/T]TGCGGTCAAGAATGC | 90293 |
rs537201418 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018466 | TAAATTAATGAGCAA[C/T]TACTACATAGCAGAC | 90293 |
rs537814419 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962853 | GATGTGTAACATTAA[A/G]CAATTAACCTCTCTG | 90293 |
rs537834077 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117970265 | AGTAATGATAAAACA[C/T]TACAAACCAATACTG | 90293 |
rs537921949 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011640 | ACTGAGTGTGAAGGA[C/T]GAGAAAGGGTCCAGG | 90293 |
rs537988525 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118055377 | TGTTAATTAAATCTT[C/G]GCATGGCATCTTAAA | 90293 |
rs538017828 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117999459 | CATAAAACCAAATAC[C/T]GCATGTTCTCACTCA | 90293 |
rs538024893 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118089499 | AGTGCCCTCCCTCCC[C/T]TGACACAGCAGTATC | 90293 |
rs538676241 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117998563 | ACCAAAGAAAGTGAC[G/T]TCTGCTCAAGGCTGA | 90293 |
rs539182207 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118101249 | TACTGCAGTTTCCAG[A/G]TGGTAAATAGGAAGA | 90293 |
rs539314676 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046672 | ATAAATATATACACC[C/T]ACTATGTGCCCACAA | 90293 |
rs539322459 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117918394 | TTAAAGAAGGTTCCA[C/T]GTTCAAAAAATGTAA | 90293 |
rs540028923 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118018242 | TATTTCCACCTACCT[G/T]ATTAATTTTTCATAA | 90293 |
rs540142386 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117924927 | ATGTTTAATGTTTAA[A/T]GTTTTTAAACATGTT | 90293 |
rs540352505 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111509 | ATGCCTGCAATCCCA[C/G]CACTTTGGGAGCCCG | 90293 |
rs540363038 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117984591 | AAAAGTAGGTGGAAA[A/G]TATTTTTTCTTTTTT | 90293 |
rs540371947 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048057 | TTGTGTGGAGTAATG[A/G]AGATGAGCTGATTAG | 90293 |
rs540597289 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901182 | ATTATGTACTATTAT[A/G]CATATTGGAAGCACG | 90293 |
rs540636555 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117925701 | GTTTGCAGAGACTTC[C/T]TTGATCTGATCCCAA | 90293 |
rs540767824 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118108017 | TTGACTTTGCACCAC[C/T]GCACTCCAGCCTGAG | 90293 |
rs541391641 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024775 | TTATTGGTGGGAGTA[C/T]AAAATGGTACAACTA | 90293 |
rs541440016 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063279 | GAAAAAGGGAATCAA[A/G]AAGTTAGAGCGAATA | 90293 |
rs541466403 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104064 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAATGCCA | 90293 |
rs541627360 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118049839 | AAGACTGGATTCCCA[A/T]GTTTCTTAGGTTTCT | 90293 |
rs542393500 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938452 | AACTTGTTAGAAATG[A/C]AAATTCCTGGGCCTT | 90293 |
rs542406205 | snp | A/C/T | 4.72358e-05 | 0.00485964 | missense | KLHL13 | GRCh38.p7 | X:117910014 | AAATTCTTCAAGACG[A/C/T]AACTGTTAACGTATT | 90293 |
rs542479811 | snp | A/G | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972929 | ACAGCAGTGGCTGCC[A/G]CGGAGAACAAGCAAA | 90293 |
rs542588029 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118032020 | CTCCCACCCGAATAC[C/T]GCGCTTTTCCGACGG | 90293 |
rs542633308 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117989790 | GTGTTCAAGCAAACC[A/T]CCCTCAGTGAAACTT | 90293 |
rs543302432 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117978793 | TCTTTATGGCTTTTC[-/T]TTTTTTTTTTTTTTT | 90293 |
rs543303178 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926118 | CAGTAAGAGAGATTC[G/T]ATTTACATTACGTCC | 90293 |
rs543627834 | snp | G/T | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:118100245 | CCACTAGTTAATTTA[G/T]GCAGTCTCCGAATGG | 90293 |
rs543750125 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986360 | CTGAAAAGAGTTCAA[C/T]ATTACTGAAAAGTGG | 90293 |
rs543923957 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117940899 | TGCAAACAGAGACAA[C/T]TTAACTTCCTCTCTT | 90293 |
rs544019985 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051191 | AGCAGCAAAGTTTGT[-/A]AAAAAAAAAAAAACT | 90293 |
rs544230584 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087257 | CTTCCCTTAACCACC[A/T]CTAGTAATGTGAACT | 90293 |
rs544246060 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998409 | TAAGAAATTATTAAC[G/T]ATGACAGAGGGTTGG | 90293 |
rs544282289 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029721 | TGCCTATAATCCCAG[C/T]ACTTTGGGATGCCAA | 90293 |
rs544424691 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948232 | ACTGTCTCATGAAAA[C/T]TTTTCTCAAGCAATT | 90293 |
rs544935975 | snp | A/C | 0.0292288 | 0.117303 | intron-variant | KLHL13 | GRCh38.p7 | X:117904085 | ATTTGTACTTTCTCA[A/C]ACAGGAGGCCCTCAG | 90293 |
rs545336480 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930551 | CATAGTTGACTTTCA[A/G]GTTGGTATGTGATAG | 90293 |
rs546217784 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092071 | GGAGAAAGGGATGGG[G/T]GTGGCAAGGGATAAA | 90293 |
rs546330138 | snp | A/G | 0.0152462 | 0.0859689 | intron-variant | KLHL13 | GRCh38.p7 | X:117944462 | ATTTTGGAGATAAGG[A/G]AAATGAAATCCGGTG | 90293 |
rs546438574 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073136 | AAAGAAGTCCTCATT[A/C]CCTCTATTTCTCCCT | 90293 |
rs546598251 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914555 | AACAAGGTACTTCAG[C/G]AGGCAGAGAATGTAC | 90293 |
rs547442950 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118058288 | CCAGAAATCCCTTCC[C/G]CTACTCCCCCCCTCA | 90293 |
rs547488196 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118078141 | CAGCAGAAGGGGCTC[C/T]TTATAGTTTAGCGTC | 90293 |
rs547503853 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109881 | CCACAAAACCGAAGG[A/G]AAAAAAAACAGGCCA | 90293 |
rs548227924 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913826 | CCAGCCTGGTGACAG[A/T]GCAAGACTCCATCAA | 90293 |
rs548437519 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117969740 | TTTTCCTGAATCTTT[C/T]GTATTTAAGATATCC | 90293 |
rs548489068 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038568 | TAGAGAGCAACAAGG[C/G]GAAAAACTCAGCCAA | 90293 |
rs548509584 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954820 | ACAGCTAGCACCCAG[C/T]CTGCCCTTTGAGAAG | 90293 |
rs548710081 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907050 | TGAATTTAGGAATAC[C/G]CTAAGAAAAGCATGA | 90293 |
rs548794799 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052859 | AGAAGACAGATAAAG[A/G]AGAATTTTTTAAAAC | 90293 |
rs548813615 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117959187 | ACTTAAAACCAAACC[C/T]TTGTTTCCAGTTTCA | 90293 |
rs548854486 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004911 | CATGAGGAACAATTA[A/C]GACTAATGAAAACTG | 90293 |
rs549318835 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979334 | ACAGAGAGACGATTT[A/G]TCATCATCAGTAGGG | 90293 |
rs549858033 | snp | A/C | 0.0343555 | 0.126481 | intron-variant | KLHL13 | GRCh38.p7 | X:118036701 | AGGACTTCATGTCTA[A/C]AACACCAAAAGCAAT | 90293 |
rs549896668 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118075519 | AGGATTAATTGAAAG[C/T]TATTGAATGGTTTCA | 90293 |
rs550016530 | snp | C/T | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117548 | CAAAACTGAGGTGTA[C/T]AGGTTAACCAAGTTG | 90293 |
rs550118393 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118017444 | TTGAATTCTGAAAAG[A/G]GAACTCTAATTAGAA | 90293 |
rs551039426 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117983898 | TAAATATATACTCGC[A/C]CCTTGGAATAATTTG | 90293 |
rs551291962 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117922052 | TATTTTTATTTTCCA[C/T]TACTAATTCGTCTGC | 90293 |
rs551328478 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950296 | ACATGGTAAAACCCC[A/G]TCTCCACTAAAAACA | 90293 |
rs552215594 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954489 | GTAAGAATCCATTCT[A/G]TTTTCTGAATGAGAT | 90293 |
rs552289605 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056732 | GGCCTTTAGAAGCTT[A/C]ATGACATAGGTTCAG | 90293 |
rs552445008 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087759 | TTCCCATCTGCTCCA[C/G]TAGACTCTTTGAGGG | 90293 |
rs552477582 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996600 | CATGCCTGAACACTG[C/T]ACCAGTAATTCACTT | 90293 |
rs552519171 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118033657 | AAATGTAAAGACCAT[C/T]GAGACTAGGAAGAAA | 90293 |
rs552542574 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118109263 | AACCAACATGTACCC[C/T]TGAAATTGCGCAACA | 90293 |
rs552674913 | snp | A/C | 0.125515 | 0.216803 | intron-variant | KLHL13 | GRCh38.p7 | X:118009323 | GACATGAAGTCCTTG[A/C]CCATGCCTATGTCCT | 90293 |
rs553223395 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041557 | AGAGACAACAAAAAG[A/T]TAAAAAGCTAGGGGA | 90293 |
rs553498448 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118090946 | TGGAATACTATGCAG[C/T]CATAAAAAATGATGA | 90293 |
rs553701715 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117910857 | TTACTTTCAGCACAT[A/T]CTGTTTCTCTCTGGC | 90293 |
rs553711191 | snp | A/G | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118032404 | GATCTGAGAACGGGC[A/G]GACTGCCTCTTCAAG | 90293 |
rs553774538 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914014 | TAGTCATCCTAAAGG[-/C]ACTTCCAACATCATA | 90293 |
rs553994714 | snp | A/C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118102452 | CCTTAAAGGAAAGGA[A/C/G]TGTGTTTTCTCCTGC | 90293 |
rs554254120 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118111592 | GTGAAACCCTGTCTC[C/T]ACTAAAAATAAAAAG | 90293 |
rs554477644 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950615 | CAACAATAACAAAAC[A/C]AAATGAAAACAAAAA | 90293 |
rs554557707 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017500 | TGGTTATTGCAGGAC[A/G]TCAGGCAAAAGATGA | 90293 |
rs554750979 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117973915 | GGTGTCCAGCAGGGA[C/T]CACTCCAAAGCTCAA | 90293 |
rs554813091 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901032 | TTTAACAGAAAAATA[C/T]ATCTTCATGTGCATA | 90293 |
rs554935148 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959763 | ATGTCAAGGTCTTAT[A/C]TCATTGATCAGTGAA | 90293 |
rs555126594 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926321 | TATTCTCCTAGAGCT[G/T]AGAGTCTGGGGACAT | 90293 |
rs555268530 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111302 | ATATTAGTAATTCTA[C/T]AGCAAAACAAAATAA | 90293 |
rs555285389 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117956692 | CTATAATTTCTGACT[C/G]TCAGTGTAGATGAGA | 90293 |
rs555339137 | in-del | -/AA | 0.0965482 | 0.197364 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985447 | AGGCTTTATATATTT[-/AA]AAAAAAAAAAAAAAA | 90293 |
rs556154674 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118013731 | TACAACTAATACCCC[A/C]ATGTTGCAGGAAGTC | 90293 |
rs556287685 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056040 | TACTTTATTTTTTCA[A/G]AGCAGATGACATGAG | 90293 |
rs556324756 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089985 | ACTCAAGAGGCTGAG[A/G]CAGAAGAATCGCTTG | 90293 |
rs556866114 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117972221 | ACTGAGAAAGATGTA[C/T]TATCAAACATATTAA | 90293 |
rs557008666 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117977769 | AGCAACCAAATAGGA[C/T]GGTTAAACCCTTTAA | 90293 |
rs557594084 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018366 | TTTTGCACGTGACAA[A/T]GTTTAGTTCTTACCA | 90293 |
rs557608589 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117931814 | TCCCTGAGCTTCAGC[A/G]TCCTTATCTATAAAA | 90293 |
rs557655898 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065827 | ATGAAACACAAATAC[A/G]GAAGAGTTATAGCTC | 90293 |
rs558479756 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044790 | ATGAAACTTCTAAAA[G/T]AAAACATTGGGGAAA | 90293 |
rs558688317 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022248 | TTATCCAGTCATCCA[C/T]TGAAAGTTGTTTCCA | 90293 |
rs558699865 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118086910 | TTAGTCCTATATGTA[C/T]CTATGATGAAATACA | 90293 |
rs558782627 | snp | G/T | 0.0404706 | 0.136372 | intron-variant | KLHL13 | GRCh38.p7 | X:117964055 | GGTGGGGTCGGGGGA[G/T]GGGGGAGGGATAGCA | 90293 |
rs558793584 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900281 | TCACTATCACTGTTT[C/G]CTTCTGCTTTTTAAA | 90293 |
rs558921279 | snp | A/G | 0.0419931 | 0.138684 | intron-variant | KLHL13 | GRCh38.p7 | X:117930238 | AGGAAGGAAGGAAGG[A/G]AGGGAGGAAGGAAGG | 90293 |
rs558975007 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026179 | TCAACCTTTCCTACG[A/T]TTTCTGTTCATTTTA | 90293 |
rs559096401 | snp | A/C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118042290 | ATTTTCAGCATTGGA[A/C/T]ACATCACCCAGACTG | 90293 |
rs559536001 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104214 | AAAACAGAATGAAAC[C/T]CTGTCTCAAAAAAAA | 90293 |
rs559646821 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117987848 | AAAACTGACCAGTTG[A/C]CTTTCCACTAACTTA | 90293 |
rs560067459 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:118064101 | ATTCACAAATATTTG[A/G]AGGATAGTTTTTCCT | 90293 |
rs560262806 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108030 | ACTGCACTCCAGCCT[A/G]AGTGACAGAATGAGA | 90293 |
rs560468783 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039650 | TGGACACACCCAGGG[C/T]CAGGGAGAACTCACC | 90293 |
rs560609604 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118032996 | AAGGGTATCAGCGAC[A/G]GAAGATGAAATGAAT | 90293 |
rs560634416 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910677 | ATAAGATAATTATCC[A/C]TAGGGCAAATTAATT | 90293 |
rs560722278 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117942484 | CTTTGTAGATCTCTA[C/T]GAACTTGCTTAATGA | 90293 |
rs561540321 | snp | A/C | 0.223547 | 0.248597 | intron-variant | KLHL13 | GRCh38.p7 | X:118019810 | ATAGTTGTAGATATG[A/C]GGCGTTATTTCTGAG | 90293 |
rs561542346 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118054156 | TGCGTTTAAGCAAGC[A/T]GGTGCAGGTTGTTTC | 90293 |
rs561825333 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076725 | GAAAAATGACTGCTC[C/T]TTTTCTGTCCCCCAC | 90293 |
rs561909800 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118101645 | CGTTTGGCTCTGTGT[C/T]CCCACCCAAATCTCA | 90293 |
rs562322101 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103089 | TCTAGTTGTGAGAAA[A/C]GGTAGCATCATACAT | 90293 |
rs562431193 | snp | G/T | 0.0414859 | 0.13792 | intron-variant | KLHL13 | GRCh38.p7 | X:117999310 | AATGTCCAACAATGA[G/T]AGACTGGATTAAGAA | 90293 |
rs562473375 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031000 | TCTTATTCAGATTCT[A/C]CAGAAAATAAACTAT | 90293 |
rs562656540 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048665 | TGTGCAGACGGGATA[C/T]GACATAGAAAGGCCA | 90293 |
rs563148170 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117904116 | TTCAAGATAGCTATT[A/G]ACCACCAATAACAAA | 90293 |
rs563233425 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117936034 | TATTTTAAAAACTGA[A/T]GGTGCTAGGAAAGTT | 90293 |
rs563842200 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114861 | CAGATTGAAAACCTT[A/G]GGCTTTTTAATAATT | 90293 |
rs564384734 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074728 | TGATTCAATGCCACC[C/T]ACCCCCAAACTGTTT | 90293 |
rs564423436 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093175 | TTACCTCATTCTTTA[A/T]GTATTTCTTCTTGTA | 90293 |
rs564543756 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117937593 | TTTTACAGAGCAAAA[G/T]ATGACATTATTCCTC | 90293 |
rs564648171 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017214 | TTAACTTGATCCATA[A/C]CTCCCTCTCCTAACT | 90293 |
rs564669114 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118033824 | AGTCAAGACCCATCA[C/G]TGTGCTGTATTCAGG | 90293 |
rs564811173 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117989758 | ACTCTACCAAGCAAA[C/T]TTCTAGTCATGCTTA | 90293 |
rs565104479 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117902043 | ATAATATCCAAACAC[C/T]TGAAACATATCTATT | 90293 |
rs565217157 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118072368 | TTAGACCTAAAACCA[-/T]TAAAAACCCTAGAAG | 90293 |
rs565547129 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902263 | TTCTCCATTTTCTTT[G/T]CTCTAAAAACATAGG | 90293 |
rs565662101 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117976946 | CCCTCATTGTATAAA[C/T]GAAAACACTGAAACC | 90293 |
rs566021565 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078758 | GTGAACATAAGCTTT[C/T]ACTTGTCTATGGTAA | 90293 |
rs566479889 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117904458 | AAGCAGTGCTTCAAT[C/T]GTAGTCTATAAGAGT | 90293 |
rs566585712 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117958520 | AACTTAACACTTTCA[C/T]GTGAAGTGATCTGCA | 90293 |
rs566588052 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118084760 | GGCCAGGCATGGTGG[C/T]TCACACCTGTAATCC | 90293 |
rs566658458 | snp | G/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986134 | GAGGGAAGCAGGCAT[G/T]TATTCTGACAATACA | 90293 |
rs566673281 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118041430 | TACTAGGGAGGTTGA[A/G]GTGGGTGGATCACTT | 90293 |
rs566913504 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117961737 | GAAGCTGAAATTGTC[C/T]TTTAACTTATAGCCA | 90293 |
rs567102872 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118006197 | AGAGGGAAAGTATTT[C/T]ACATACAAAAATGGT | 90293 |
rs567245902 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939190 | GTGAGAACATCTGGT[A/G]TTTGGTTTTCTTTTC | 90293 |
rs567514894 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118075289 | ATACTGAAGGGTTTA[C/T]GTGTAACTCAAAAAA | 90293 |
rs568065516 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013954 | CTTATGCCTGTCTTT[A/G]CTTTAATCTCTTAAT | 90293 |
rs568155001 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037257 | GGGTATATACCCAAA[G/T]GACTATAAATCATGC | 90293 |
rs568220910 | snp | C/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118245 | ATTCCCCTTTGTTAA[C/T]AGGAATGCTTCCACT | 90293 |
rs568566166 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924190 | CAAACAAATTCTAAA[C/T]ATCTTGTTTGTATAT | 90293 |
rs568864192 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117909189 | AAAAATAGTTTTAAA[A/C]TAAAACCCTAACTAC | 90293 |
rs568940871 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117992763 | ACCCCCAGCACTCCC[C/T]TTTTCTTTCTAAACT | 90293 |
rs568967959 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117919085 | CTGGAGTGCAATGGC[A/G]TGATCTCAGTTCGCC | 90293 |
rs569293216 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118063952 | AGCAATTACACCCTA[A/G]CAGCTGTTATATATT | 90293 |
rs569510097 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924303 | CTCTAAACACCTTTT[A/G]TTCTCTAATCTTCTA | 90293 |
rs569546825 | snp | C/G | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:117956721 | GAAGCAGACAAAAGG[C/G]GAGAAGAGTCACCAT | 90293 |
rs570224049 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975164 | GTTTGAAATCCAAAG[A/G]AGGAGAAATACATAC | 90293 |
rs570330328 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117934133 | AACACTGGGATTCTA[A/G]AAGGAGGAAGGGAGA | 90293 |
rs570456221 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118106166 | CCTCCCAAAGTGCTG[C/G]GATTACAGGCATGAG | 90293 |
rs570554296 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117914656 | AGAACAAAGGGATAA[A/C/T]TGAATAATAAACACC | 90293 |
rs570702096 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088958 | ATAAAGCTGAAGAAG[C/T]TGGCAACCTAGAAAT | 90293 |
rs570740882 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118115395 | GCGATATCGCTAAGA[A/G]TGAGTAGTCTTTTTT | 90293 |
rs570835595 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011179 | AGAGAGGTCCTGAAT[A/G]ATAAACAGGAATGGG | 90293 |
rs570868500 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117968333 | AGAAGGACATGCAAT[A/G]CCATCTTCGAGAGGT | 90293 |
rs571029033 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117934674 | GTAAAATATATATAT[A/G]CACATATATGTAATA | 90293 |
rs571114588 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917564 | AGCAATACAAAGTGA[A/C]TATGGTCTCATCTTT | 90293 |
rs571134626 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118026760 | ACCCAACACCATAGA[A/T]ACCACAGTTGGTTCA | 90293 |
rs571321939 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069548 | CCTTACATTTATACA[A/G]ATAAAAAACAATATT | 90293 |
rs571583864 | snp | G/T | | | missense | KLHL13 | GRCh38.p7 | X:117945480 | GTAAAGATGCGTGTA[G/T]GTCCTGCCTTGGAAG | 90293 |
rs571584663 | in-del | -/TAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118002643 | AAATAAATAAATAAA[-/TAAA]ATGCTGTGGGATGGA | 90293 |
rs571962170 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118091367 | GCCATCATAAAAATG[C/T]TTCATTGAGCAATTA | 90293 |
rs571995550 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117965415 | CTGTTAATATCCTTC[A/G]CCCACTTGTTGATGG | 90293 |
rs572073493 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117934874 | AATGGCCATAAGCAT[-/A]AAAAAAAAAAGATAT | 90293 |
rs572582258 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024760 | AAAGATTCTCACTTA[G/T]TATTGGTGGGAGTAT | 90293 |
rs572666113 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118068443 | AGTCACATAAAGAAC[A/G]GAAGGAAATACTAGG | 90293 |
rs572885979 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082015 | ATCCAGTCATCCTTT[A/G]ACATACAGTTAGGTT | 90293 |
rs572948628 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981431 | GTAATCTAAATCTGG[G/T]TTTCTTGACTTCCTT | 90293 |
rs573027980 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017616 | ACCCTCCCAAGACCC[A/G]GTGTATATATGTGTT | 90293 |
rs573079787 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940066 | CTTCCAGGGTTTTTA[C/T]GGTTTTAGGTCTTAC | 90293 |
rs573122205 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981897 | TGTCAACTAAAATAC[A/G]GTTATTTCAACTGAA | 90293 |
rs573306153 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900888 | TCCTAAATTCTACAG[A/G]AGAATGAAAGCAGAA | 90293 |
rs573307540 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928057 | TAAACCTAGCATGAC[C/T]ACAATACCAAACAAA | 90293 |
rs573927907 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117989783 | TGCTTAAGTGTTCAA[G/T]CAAACCTCCCTCAGT | 90293 |
rs574522017 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057749 | GAGAATGGTGTGAAC[C/G]TGGGAGGCAGAGCTT | 90293 |
rs574597909 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118047223 | AATTTAAAGGTAACA[A/G]AATGAAGCTGAAAGA | 90293 |
rs574607468 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089995 | CTGAGGCAGAAGAAT[C/T]GCTTGAACCGGGGAG | 90293 |
rs575123455 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000406 | AACATCCAAAGATTA[C/T]AACCAACAGCAATGT | 90293 |
rs575130997 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117937088 | TTCCCCTGACAGCTA[C/T]TTTCAATGCCTTTTG | 90293 |
rs575186713 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117972440 | ATTCAAACAAATCCA[A/G]CATATGTTAAATATT | 90293 |
rs575805215 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118106800 | AGTCTATCCCTCTAA[C/T]ACCTAAAGCTGTTCT | 90293 |
rs575941898 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118054009 | AAAAAGACAATGAAG[C/G]AGAAAGAAGAAAAAC | 90293 |
rs576256333 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118100244 | GCCACTAGTTAATTT[A/C]TGCAGTCTCCGAATG | 90293 |
rs576555968 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045373 | AGCAAGACTCCATCA[-/A]AAAAAAAAAAAAAAA | 90293 |
rs576877209 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000658 | AAAATTCAAACACTT[A/G]GAAATCAATTTTTTC | 90293 |
rs576923744 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093478 | GAGTCCACAGTCTTA[A/C]TTAAAACTATACCAT | 90293 |
rs577027016 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118023121 | ACAGTTTTCCCAGCA[C/T]TATTTATCTTCTAGG | 90293 |
rs577067268 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052381 | ACAAAAAATTAGCCA[A/G]GCGTGGTGGCAGGCG | 90293 |
rs577119731 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930318 | AGGCAGGCAGGCAGG[A/C]AGGAAGGCAGGAAGG | 90293 |
rs577273993 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060799 | TCATTGTATTAGTTT[G/T]CTGGGGTTGCCATAA | 90293 |
rs577486502 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117919339 | AACACAGAGGCTTTT[A/G]TTAAATGATTCTATT | 90293 |
rs577887080 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903054 | AATTAGGTTTAGCTA[C/T]TTGCAACCAAATGCA | 90293 |
rs745309081 | in-del | -/AAGAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113994 | AAAGCCATTTTTATA[-/AAGAC]ATTTTGAGATATTTT | 90293 |
rs745329344 | in-del | -/TTAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908070 | CTACAAGGACATTAT[-/TTAT]TTATTTATTTATTTA | 90293 |
rs745333045 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117940306 | ATTTGTCTATATATC[C/T]GTTTTGGTACCAGTA | 90293 |
rs745333694 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085612 | CTTCTGAGATTCCAG[A/T]GTCCATGATATCACT | 90293 |
rs745338857 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013928 | TTCCTCAATCAATAC[C/T]CTTATAATTTCTTAT | 90293 |
rs745343568 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117949869 | TTCTTGGTAGAGAGG[G/T]TATGTGTGCCAATTC | 90293 |
rs745349687 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072436 | CAAGGACTTCATGTC[C/T]ACAACACCAAAAGCA | 90293 |
rs745350885 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991455 | TCTAATTCAAAATTT[A/G]GAATTCATTTTGCCA | 90293 |
rs745372805 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117930910 | TCTTAATCATTATGC[C/T]TGTTTCTTATGTTAA | 90293 |
rs745379373 | snp | A/C | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118097410 | GAGAACTACAAACCA[A/C]TGCTCAAGCAAATAA | 90293 |
rs745390605 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018358 | CATCATGCTTTTGCA[A/C]GTGACAATGTTTAGT | 90293 |
rs745391361 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117992436 | AACCATGTATATTAT[G/T]TGTCATGTCCAAACA | 90293 |
rs745396972 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066919 | ACGTGCCCATGAACA[C/G]AATGAGACAATTCTT | 90293 |
rs745398744 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941034 | GCCAGTTTTCAAAGA[G/T]AATGCTTCCAGCTTT | 90293 |
rs745410121 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117908291 | GGTACATGTGCAGAA[C/T]GTGCTGTTTTGTTAC | 90293 |
rs745415040 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015445 | TTTAGTCTGGGACTC[A/G]GAAAAAATTGAGACT | 90293 |
rs745415726 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118041293 | GTACTTTGGGGGACC[A/G]AGGTGGGTGGATCAC | 90293 |
rs745436604 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118064465 | CTGAAGAAGCCACTG[C/T]TATTTTAAAATATTG | 90293 |
rs745449872 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117962110 | CAGTTACTGAGGAGG[C/T]TGAGGCAGGAGGATC | 90293 |
rs745458273 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018812 | AGACAAAAGGTACTG[G/T]TTTTAAAAATTTTTA | 90293 |
rs745466285 | snp | C/T | 0.00115569 | 0.0240106 | utr-variant-5-prime, intron-variant | KLHL13 | GRCh38.p7 | X:117985292 | TCATTTGTCATGTTC[C/T]TGTGGATCCCTCTCT | 90293 |
rs745468891 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118088614 | TATTGACAAAGCAGC[A/G]AAATAGAATATAAAG | 90293 |
rs745470749 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118011866 | GCGCTTTCAGTGCAG[A/T]GGGATTATACTTTCC | 90293 |
rs745477941 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117992030 | ATGAGGTGGCTATCA[A/G]TTATTCACACATTGG | 90293 |
rs745478297 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915157 | TTGCCCTCAAAAGTG[-/A]AAAAAAAATCTTAAA | 90293 |
rs745485796 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118816 | GACTCAGAGTCAGAA[C/G]ACAATTTATGTGCTA | 90293 |
rs745488858 | snp | A/G | 2.29056e-05 | 0.00338412 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909464 | CGTTTTTCCTTTTGT[A/G]TCATAATTACTCTGT | 90293 |
rs745500019 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118033331 | GAAAAAATGTTAAGG[A/G]CAGCCAGAGAGAAAG | 90293 |
rs745508918 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117953534 | ATTGTGCACATGTAC[C/T]CTAAAACTTAAAGTA | 90293 |
rs745520149 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118053422 | GAATGTTCTCACTCA[C/T]AGGTGGGAATTGAAC | 90293 |
rs745535634 | snp | G/T | | | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897371 | AGATAAAGTAGAGAA[G/T]ATCACAATACGATGC | 90293 |
rs745545127 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118012667 | GGATTAAAATGTGGC[C/T]ATCCTGGGCGGGGGC | 90293 |
rs745556085 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118003765 | CCTTACCATGGTTGT[-/A]AGGAAAAAGGTGGCA | 90293 |
rs745565398 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030964 | CCTCCTACTGTGCCT[C/G]GATTTCTGAGTCTGG | 90293 |
rs745566508 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083668 | GTTCTATTGCATGGC[A/G]GGGTGACTACAGTTA | 90293 |
rs745567732 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092079 | GGATGGGGGTGGCAA[G/T]GGATAAAAGACTTCA | 90293 |
rs745569201 | in-del | -/CAATAAAACTCAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117987838 | TTGAGTGAAAAAACT[-/CAATAAAACTCAAA]GACCAGTTGCCTTTC | 90293 |
rs745569700 | snp | A/C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime, downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117898105 | TTCAGTATGTGCATA[A/C/T]TGAATTCCCATTTTA | 90293 |
rs745576475 | in-del | -/TTAGACCA | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118109227 | AACACATGTTTAGAT[-/TTAGACCA]TTAGACCAAGGGTAA | 90293 |
rs745595960 | snp | C/T | 4.56308e-05 | 0.00477633 | missense | KLHL13 | GRCh38.p7 | X:117899174 | TGGCAGCAATTGGGG[C/T]CCACTGGTCAAGGAT | 90293 |
rs745614833 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118033575 | AGGCCTGCCCTAAAA[C/G]AGATCCTGAAGGAAG | 90293 |
rs745628800 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046368 | ATGGAGACAGATGGT[A/G]GAATGATGGCTACCA | 90293 |
rs745641345 | snp | A/G | 0.0323082 | 0.122924 | intron-variant | KLHL13 | GRCh38.p7 | X:118096909 | actctcaataaatta[A/G]gtattgatgggacgt | 90293 |
rs745644074 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118004412 | CTAAAAGGAACCATG[A/G]TGCCTGATTCCAGAG | 90293 |
rs745650774 | snp | G/T | 0.00151719 | 0.0275008 | intron-variant | KLHL13 | GRCh38.p7 | X:117983450 | GAAAAAAAAAAAAAG[G/T]TGAGGAAAAATGTAG | 90293 |
rs745693464 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005077 | GAAGTTGAGCTTTCT[A/G]CTGTCAATAACACTT | 90293 |
rs745695793 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026173 | CCTACCTCAACCTTT[C/G]CTACGTTTTCTGTTC | 90293 |
rs745697902 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118021486 | TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTCTG | 90293 |
rs745702536 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954210 | TTGCTCCCTCTGCTT[A/G]CCATATTTCAAGACT | 90293 |
rs745710851 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029673 | GCAATTTAGTTTATT[A/C]ATAAAGTTATGTTGG | 90293 |
rs745721682 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118077243 | GCAATCAAACATCTA[C/T]ATGAGGCAATGCCAA | 90293 |
rs745722524 | snp | C/T | 6.96799e-05 | 0.00590213 | intron-variant | KLHL13 | GRCh38.p7 | X:117945424 | CTACCAAAGAGACAG[C/T]TTAAATTACCTGTAA | 90293 |
rs745722745 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904420 | GAGTAAGGGATGATG[A/C]AAGGCAAAGAGTTGG | 90293 |
rs745747540 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102118 | GGACAGGCAGGAGTC[A/C]AGTCATGATGGACTT | 90293 |
rs745748031 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117913717 | ACGTGGTGGCACACG[C/T]CTGTATTCCCAGCTA | 90293 |
rs745774153 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118095136 | CCAGTGTGCTGCATT[A/C]AGGAAATGCATCTCA | 90293 |
rs745794311 | snp | A/C | 2.32261e-05 | 0.00340771 | intron-variant | KLHL13 | GRCh38.p7 | X:117920422 | TAAAATGAGGTTACA[A/C]ATCTTCGTGTGCTAA | 90293 |
rs745802189 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114837 | TTTGAAGTGTGCTTA[G/T]AAAAATGGCAGATTG | 90293 |
rs745803009 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118037811 | AAGAGAGATAGACTA[C/G]ATATCTAGAGATCAG | 90293 |
rs745809638 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070229 | TCGTTAAGTGATGAA[C/G]GCTGTGTAAGCATTT | 90293 |
rs745815551 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117997839 | TTGTAAGTACCCCTG[A/G]AGGCACCCACAAAGC | 90293 |
rs745816431 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117925849 | CTAGCTTAAATTAGA[C/T]CTCCTTTGTTGTTGT | 90293 |
rs745831458 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117909050 | CCTTCAAGATGAAGA[C/T]CATATATACTGCACA | 90293 |
rs745867998 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118038346 | ACAACCAAAAATCAG[A/G]TGAATGATCACAATA | 90293 |
rs745872297 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905062 | AGAAAATCATTTAAA[C/T]AGTGATGGCTGTCAT | 90293 |
rs745873663 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016095 | TATGAAGTTAATCAC[A/G]TATGTGTTTCTTTAG | 90293 |
rs745884934 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045131 | GTAATCCCAGCACTT[C/T]GAGAGGCCAAGGCAG | 90293 |
rs745902120 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938721 | TAGTGAGGTATTTCT[A/T]ATTTTTCTTTAGCGA | 90293 |
rs745915715 | in-del | -/TTTAT | 0.0209675 | 0.10022 | intron-variant | KLHL13 | GRCh38.p7 | X:118070766 | TTATTTATTTATTTA[-/TTTAT]TTATTATACTTTAAG | 90293 |
rs745917725 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117927053 | TGGGACTATAGGCGC[A/C]TGCCGCCACGCCCGG | 90293 |
rs745931375 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117988984 | GATATACATGCCAGA[A/T]CATTAGGAAGTTTAA | 90293 |
rs745932728 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089098 | CTCTACTCCAGCTAA[A/C]CACTACAGAAAAAAA | 90293 |
rs745938943 | in-del | -/TTC | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117943 | GCTGTTTTTTTCTTC[-/TTC]TTCTTCTTCTTAAGG | 90293 |
rs745943175 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007660 | TATATCAGCTATGTC[A/G]TGCTGTGCTGATATA | 90293 |
rs745947299 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117979077 | CTGGGATTACAGGCA[G/T]GCGCCACCACGCCCG | 90293 |
rs745953313 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039871 | CACCTCTCCCTCAGC[A/T]CTAAACAACTCAGAA | 90293 |
rs745953870 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985971 | AAAAATAAAACTACA[C/T]ATGATGTAAAGTAAA | 90293 |
rs745970191 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117918590 | GGCAATATTTCTGTC[A/C]AATGTAGCCATTTAT | 90293 |
rs745974413 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118114940 | AGAAACTACTCTCAT[A/C]TCACTGCCATAAGAC | 90293 |
rs745982012 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987118 | TACCTCACAGCCCTG[C/G]TTCAAAAATTCCAGG | 90293 |
rs746006679 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967782 | TAAAACAAAATGTTA[A/C]CTTCATTTGCACATG | 90293 |
rs746010429 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001210 | AACCACTGCCATTAG[-/A]AAACTTTCTACTCAG | 90293 |
rs746012258 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117960044 | TAAATTTTAGTGCTC[C/T]AAAACACAATATTTT | 90293 |
rs746019687 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081217 | CTGCATATGTGTACA[C/T]CCTGTATCTAAAATA | 90293 |
rs746024734 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117936841 | AATATTTATTATGCA[A/C]CTTATTTCCATAAAT | 90293 |
rs746030108 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005866 | AAGACATGGGCCTAA[A/G]AATAGCTGGAAAGAA | 90293 |
rs746043146 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941830 | CCTCGTGTCTCTATC[C/T]CCTTCAGTTCTACTC | 90293 |
rs746046859 | in-del | -/AAGG | 0.293331 | 0.246216 | intron-variant | KLHL13 | GRCh38.p7 | X:118099919 | AAGAAGGAAGGAAGA[-/AAGG]AAGGAAGGAAGGAAG | 90293 |
rs746058863 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118026207 | TTACAACATGCCTGT[A/G]TTTTAAAATACCTCG | 90293 |
rs746062029 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118009278 | CATTTGTCAATTTTG[G/T]CTTTTGTTGCCATTG | 90293 |
rs746065564 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118079180 | TTGAAATTGTAAATT[A/C]GCAGAAAAAGAAATG | 90293 |
rs746067405 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951609 | AGATTTTATAAAATA[C/G]CTGCTATCTTTCCAA | 90293 |
rs746093049 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117918568 | CTCCAAGACCTCTGG[A/T]AGTCTTGGCAATATT | 90293 |
rs746110343 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081636 | TTTGAAATATTCAAT[A/G]AATTATTGTTAACTA | 90293 |
rs746111673 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118051953 | AGTGGATATTAAAAT[A/G]TAGTAAAAAATATAT | 90293 |
rs746117986 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938248 | TTTTGGTGCAACATA[C/T]TTCATGCAACGATTC | 90293 |
rs746119959 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073870 | ATCTGTCAGGGAGGT[C/G]ACTCTAGATCAAATC | 90293 |
rs746134971 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118058022 | CAGGCACTGGTACAC[A/G]TTTTCTAGGCTTTTT | 90293 |
rs746144210 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080448 | CCCCATTAAAAAAAC[A/G]GGCAAAGGACATGAA | 90293 |
rs746145209 | in-del | -/TT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099235 | TATTTATGCATTTCA[-/TT]TTACACCATCTGAAA | 90293 |
rs746162936 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019584 | TGCCTATGTTCTGAA[C/T]GGTATTGCCTAGGTT | 90293 |
rs746184093 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074750 | AAACTGTTTCACTAT[-/A]AAAATTTGATAAGAT | 90293 |
rs746185108 | snp | A/G | 0.0230396 | 0.104828 | intron-variant | KLHL13 | GRCh38.p7 | X:117963959 | AAAAAACCAAACACC[A/G]CATATTCTCACTCAT | 90293 |
rs746187962 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118043112 | CTACTATGAGCAAAT[A/G]CATGACAATAAATTG | 90293 |
rs746197575 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917408 | TAGGATGTCTGCAAA[-/G]GATGCAAAAAAAAAA | 90293 |
rs746205227 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994031 | GTGAGCCACCACGCC[C/T]GGCCTGCTGCATTTA | 90293 |
rs746207631 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942730 | ATGTGTGTCTTTGCA[C/T]GTGAGATGGGTCTCC | 90293 |
rs746218852 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093111 | TGAGTAATTTGCCTG[C/T]TAAAAGTGCCTCCAC | 90293 |
rs746223262 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117934101 | GGTACACATGGACAC[-/A]AAAAATGGAAATAAT | 90293 |
rs746225561 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117946628 | ATACAGACTGCTAAA[A/C]AGACTGCTAAAATAG | 90293 |
rs746227089 | snp | C/G | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118020206 | CTTGAAGAGGTCCTT[C/G]ACATCCCTTGTAAGT | 90293 |
rs746247043 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074520 | GCTGCTGCTTTCTGT[A/G]TGAGCTGGCTGGAGC | 90293 |
rs746260664 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048585 | CATGTTTGGAATTTT[C/G]TAATAAAGAAGAAAC | 90293 |
rs746278770 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948649 | TTTTGTTTCTAAAAA[C/T]TAAACCTCTCTTTTC | 90293 |
rs746280568 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928943 | AAACTCTAACAAGAC[A/G]GATTAGGTGAGAAAA | 90293 |
rs746296319 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117964427 | TAAGCTATTTAATTG[C/T]TTATGAATGAAGATA | 90293 |
rs746312801 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013817 | ATTTCATGGACATTT[A/G]TCAATTCCCAAAATT | 90293 |
rs746315648 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117901675 | ACACCCAGTTAATTT[C/T]TGTATTTTTAATAGA | 90293 |
rs746318889 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968715 | TTCTCTAATCACAAA[G/T]GATTATCAATTTAAT | 90293 |
rs746321899 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093807 | TGTTATACAAGCATA[A/G]GAAGTATGATGGGCT | 90293 |
rs746331710 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985464 | AAAAAAAAAAAAAAA[A/G]CCTATGTACTGCATA | 90293 |
rs746333691 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944816 | CTAAATAGCTCCAGA[A/T]TGCTGTGTTTCATGT | 90293 |
rs746343852 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936031 | TATTATTTTAAAAAC[C/T]GAAGGTGCTAGGAAA | 90293 |
rs746359259 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924746 | GTTTGATTTAAGAGG[A/G]GTTTGTCTGTCCTCA | 90293 |
rs746362551 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014713 | TCTTCTCTTTGTACT[-/C]TGTCTCTTTATTTCT | 90293 |
rs746369619 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118036292 | CATCACCAAGGCAAT[C/G]CCAAGCCAAAAGAAC | 90293 |
rs746370227 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117975930 | TAAGTTATTATTCTT[C/T]TATAAACAATCAACT | 90293 |
rs746412777 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117915258 | TGCAGGAAATCCTCA[A/G]TAATTTAGTAACAGA | 90293 |
rs746416035 | in-del | -/T | 0.0384368 | 0.133195 | intron-variant | KLHL13 | GRCh38.p7 | X:118085945 | ATGCATGAAGATGGA[-/T]TTTTTTTTTTGAGAC | 90293 |
rs746422922 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118091623 | ATAAACTGAAAAAAA[C/T]ATGAATACAGAATTA | 90293 |
rs746423148 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017146 | GTAAGCTTCAGTAGA[C/T]CTCTGCAGTCTGTGA | 90293 |
rs746430970 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111851 | GAGCCGGGATCATGC[C/T]ACTGCACTCCAGCCT | 90293 |
rs746435640 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082499 | CCTTACATATTCTGG[A/G]TATTATCTCCTTGTC | 90293 |
rs746436201 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040675 | GGGAACTTCCCAAAC[C/G]TAGAGAAAGATATCA | 90293 |
rs746443037 | snp | C/T | 2.45975e-05 | 0.00350687 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898883 | GCAAAGATAGAACTA[C/T]AGCATCTTAGTTGTA | 90293 |
rs746469156 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031187 | ATGGGAAGAATTAGT[C/T]GGTTTCTCTCAGAAG | 90293 |
rs746473312 | snp | C/T | 2.29132e-05 | 0.00338468 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909446 | GAAGACTGTATCAAC[C/T]GCCGTTTTTCCTTTT | 90293 |
rs746480805 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029657 | TAAAAATGCATAATA[C/T]GCAATTTAGTTTATT | 90293 |
rs746485802 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956981 | AATTTCAGAAATCTC[C/T]GATGTATCCTGATAT | 90293 |
rs746508480 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981341 | TTATCTCATGGTCTA[C/T]TACTAACCAAAGTAA | 90293 |
rs746518342 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977197 | TCCAATTATATGTTC[A/T]CTGAAAAATAGAAGT | 90293 |
rs746537845 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939875 | GATTGCAAAAATTTT[C/T]TCCCATTCTGTAGGA | 90293 |
rs746538997 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948301 | CATGAGGTAATGCTA[G/T]CAATATGAAACACAG | 90293 |
rs746559837 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959900 | GGTGAGAGACTTAAA[C/T]GTGGGAAGCAAGAAG | 90293 |
rs746561547 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023413 | AAGGGCTCTTTTCTA[C/T]TCTTAAAAGGAGCAT | 90293 |
rs746567286 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968015 | AGAATTGTCTTCTAT[G/T]TGGGCCCCATGTGGA | 90293 |
rs746568477 | in-del | -/T | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118000561 | GAAATTTCAAAAACA[-/T]TTTTGGGGTCCTACA | 90293 |
rs746569201 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048652 | GGGACTATGTAGATG[C/T]GCAGACGGGATATGA | 90293 |
rs746579793 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039505 | GGCTCCTCTGCTTCA[A/G]GAAAGGAGGGGGAAA | 90293 |
rs746590745 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096803 | AAACGTAATCCAGCA[C/T]ATAAACAGAACCAAC | 90293 |
rs746601458 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118065449 | CTTTGGGCCATGCTG[A/T]TTAGACCAGAAGTGG | 90293 |
rs746604124 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907559 | GTCACTACTTGCACC[C/T]TCTAGATATTTCCAG | 90293 |
rs746617391 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118116437 | ACTCCTCGCCGCGCA[C/G]CGCGCAGCGCCGGGT | 90293 |
rs746623475 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118024010 | TTAGAATCAGAATTA[C/T]ATTTCTTTCAAAGGG | 90293 |
rs746629038 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913510 | TCACTTAAAAACAGA[G/T]TTATAACAGAAGTTA | 90293 |
rs746630977 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117990437 | TTTGTTACCACCTAG[A/G]CCAGGGAATATTGAA | 90293 |
rs746652326 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914842 | TTGTGAGGTTGAAGA[C/G]GTTTGAGCCCAGGCT | 90293 |
rs746656304 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104688 | GTCTGTGTTAGACTG[A/C]GCATAAATCATGAAC | 90293 |
rs746661108 | snp | A/G | 1.64985e-05 | 0.0028721 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972880 | TTTCCATAACAGACT[A/G]CCAACTAAGACTTCC | 90293 |
rs746663734 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117929793 | CAAAAAAAAAAAAAA[A/C]AAAAAAAAAAACTTA | 90293 |
rs746664768 | in-del | -/A | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117968794 | TATTTACTAAATTAG[-/A]AAAAAAAAGACAATC | 90293 |
rs746674322 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071926 | AATTTACAGATTTAA[C/T]GCCATCCCCATCAAG | 90293 |
rs746682529 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961432 | TTGTGTTCAACTAGA[C/G]TATTGTAGATACAAC | 90293 |
rs746695229 | snp | G/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:117908099 | TATTTATTTATTTAT[G/T]TATTTATTTATTTAT | 90293 |
rs746695615 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118090557 | GGCCATCAGAGAAAT[G/T]CAAATCAAAACCACA | 90293 |
rs746703672 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117930707 | ATGCACAGTCAATTC[A/G]AAGAATAAGAATAAC | 90293 |
rs746707659 | snp | C/T | 3.41338e-05 | 0.00413107 | intron-variant | KLHL13 | GRCh38.p7 | X:117901995 | TAACTTCAAATTTAG[C/T]AATTAATTATTTTTC | 90293 |
rs746713856 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118033080 | AAGCCTCCAAGAAAT[A/G]TAGGACTATGTGAAA | 90293 |
rs746728611 | in-del | -/AAATAAAT | 0.0105901 | 0.0719924 | intron-variant | KLHL13 | GRCh38.p7 | X:118011074 | TGAGACACTGTCTCA[-/AAATAAAT]AAATAAATAAATAAA | 90293 |
rs746728676 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118018331 | CAATGAGTAGAAGAA[C/G]TCATCACTTTTCATC | 90293 |
rs746733990 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114592 | GAGAATAGTTTGCTA[A/G]GAAAATTACAGACTT | 90293 |
rs746739613 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:117952575 | TAATTAAACTAAAGA[A/G]CTTCTGCACAGCAAA | 90293 |
rs746741326 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117618 | AGGATCCCAAGCGGT[A/G]TGATTCTGGTACCCA | 90293 |
rs746754106 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118043197 | ACCCATGAAAAAATC[C/T]AAAACCTGAACAGAC | 90293 |
rs746756714 | snp | A/T | 1.6473e-05 | 0.00286988 | intron-variant | KLHL13 | GRCh38.p7 | X:117920206 | TTTCATATTGTTTTA[A/T]TGTGGTTTCAGAGTT | 90293 |
rs746764170 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118064410 | AATTTAGCATGCATT[A/T]AGGTTTAGAATATAA | 90293 |
rs746778908 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117981779 | AAGCACAGAACAACA[-/T]TAACATGTATTCCAA | 90293 |
rs746780953 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022749 | TAACCCTCATCACAT[A/G]TATGGTTTGCAAATA | 90293 |
rs746783643 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118091350 | ACAAAGATTTTAAAG[G/T]AGCCATCATAAAAAT | 90293 |
rs746791215 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117921482 | GATACAAAAAATGAA[C/T]ATTTTGGCAAGATTG | 90293 |
rs746793607 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117992207 | CCTTGAGGGATAGAG[A/C]AACTTTCTCTTAGAG | 90293 |
rs746813370 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044854 | TGAGCAATACCTGAT[A/G]AGCACAGACAACCAA | 90293 |
rs746814367 | in-del | -/TGGGG | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118011795 | TCATGTTTACAATAC[-/TGGGG]AATCTTTGTGTTGAA | 90293 |
rs746817066 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991909 | TGTAACCCTCACCCC[C/G]CTCCCACATTGTTTG | 90293 |
rs746824125 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117972499 | TATGCCTTTGTACTT[C/T]CACACTGGTAATTAG | 90293 |
rs746829467 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118028160 | ATTCAAATAAATATC[G/T]CCACTGATTGTATTC | 90293 |
rs746843361 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118033300 | AATTGTCACATTCAC[C/G]AAAGTTGAAATGAAG | 90293 |
rs746863983 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118053374 | AAACCATCATTCTCA[A/G]CAAACTATTGCAAGG | 90293 |
rs746869567 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906597 | GACTCTTTTTGGCCT[G/T]TTTTCTCCTGAAATC | 90293 |
rs746873674 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118083702 | ATAATGTATTTTAAA[A/G]TAGAAGAGAGGATTT | 90293 |
rs746873937 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117982746 | ACTAAACTATTAGAG[-/A]AAACACTGCTTTAAA | 90293 |
rs746894716 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075679 | AGAGGAAGGGGGAGA[C/G]GAAAAAGAAAATCAT | 90293 |
rs746911050 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117941368 | AAAGAGTTAGGGAAT[A/G]TTCCATCTTTTTCTA | 90293 |
rs746911910 | in-del | -/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118054313 | ATGAGATTCACAAAC[-/T]TATCTTAAAACAAAA | 90293 |
rs746914171 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912056 | GAGGAGCTGCAGGTC[A/G]GTGGTTCAAAAATTT | 90293 |
rs746919382 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029037 | CAAAAAAACATAGTA[C/T]ATATAGGGTTCGGTA | 90293 |
rs746927027 | in-del | -/G | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118003673 | ATAATTTTAAAATGT[-/G]GATGTTGACTACAGG | 90293 |
rs746931275 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944555 | TTCTATATACAGCTT[C/T]ACTATAATGGTTCTT | 90293 |
rs746933008 | in-del | -/ATCT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045000 | ACATGTAAACCATCC[-/ATCT]GACAAGTGATTAATA | 90293 |
rs746958504 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922387 | CAGCTGAAACAGTTG[A/G]GAGACTAGCATCTTT | 90293 |
rs746972845 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113240 | ATACTGATCATAGAG[A/T]TTTTTTTATTCTCAG | 90293 |
rs746983066 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923677 | CCTCTGAAAAGAGGA[C/G]TAGCTTGTGCATCAT | 90293 |
rs746994671 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101516 | ACATGAAAGAAACAC[A/G]TAACAGGGGTGTGAG | 90293 |
rs746994682 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118094448 | CAGGGAGAATGGAAC[C/G]AAGTTGGAAAACACT | 90293 |
rs747008959 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021341 | GTTTGCTGCACCCAT[C/G]AACTCGTCATTTACA | 90293 |
rs747018822 | in-del | -/A | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118036723 | AAAAGCAATGGCAAC[-/A]AAAGCCAAAATTGAC | 90293 |
rs747024639 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117965549 | ATCCTCCCTAACTCA[C/T]TTGATGAGGCCAGCA | 90293 |
rs747026518 | in-del | -/C | 0.0287145 | 0.11633 | intron-variant | KLHL13 | GRCh38.p7 | X:118069441 | AAAAAAAAAAAAAAA[-/C]AATTTTAAAAATAGA | 90293 |
rs747038789 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926898 | CTTCTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTT]TTTTTTGAGATGGAG | 90293 |
rs747059951 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987197 | TGACCTTTGGAAAAA[C/T]AGAGCTGTAAGTGGA | 90293 |
rs747060880 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938015 | AAATCACATAAAACA[C/T]GGACTTTGGTGATTA | 90293 |
rs747064918 | in-del | -/AGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998092 | AAGGCAAATAGATGG[-/AGA]AGGAGAGAAGAGTGA | 90293 |
rs747076755 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004881 | CCTGCTGAAGAAGCA[A/G]AACCTCAATAATATC | 90293 |
rs747077650 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005691 | AGGTGGCCTCTGGAC[A/G]CTGGGAAAGGCAAGG | 90293 |
rs747084431 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118095043 | TCACACATAACAATA[C/T]TAACCTTAAAGGTAA | 90293 |
rs747096891 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021782 | TGGGTCAAATGGCAT[C/T]TCTGGTTCTAGATCC | 90293 |
rs747106374 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113024 | CCATGAGAAAATAAG[A/G]TATCATTCTTTGAAA | 90293 |
rs747110536 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118037762 | TAATTAAAAAAAAGA[A/G]AAGAAAATTAGCACA | 90293 |
rs747120560 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958329 | TATAACAATATACTT[C/T]AATAAAAGTTATGTG | 90293 |
rs747121421 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904258 | CTCCATGCAGAGTTG[C/T]TATTGTTATCAGTAA | 90293 |
rs747149638 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117965961 | TCATACTGAATGAAC[A/C]AAAACTGGAAGCATT | 90293 |
rs747153142 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007997 | TCGAATGGAGGGAAG[A/G]GGTCAAAATATCACA | 90293 |
rs747156941 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950998 | TTAAGATGGTAGAAG[C/T]CATTTTCCATTGGCT | 90293 |
rs747200418 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113681 | GCCTTTTCTGACTTC[C/T]CACACTAAAGTAGGC | 90293 |
rs747200660 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908649 | TACATCAAAGTACAT[C/T]TATGACCAATTTTAT | 90293 |
rs747202545 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104935 | GTTAAATATTTTTTT[C/T]GACACAGGATTGTGA | 90293 |
rs747202803 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032174 | GGGGGAGGGGCGCCC[A/G]CCATTGCCCAGGCTT | 90293 |
rs747220040 | snp | C/T | 2.48945e-05 | 0.00352798 | intron-variant | KLHL13 | GRCh38.p7 | X:117899424 | ACAATAGTTTTGAAG[C/T]AAATAATTATAGAAA | 90293 |
rs747222574 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089017 | AGAAGAAAAGTCTGC[C/T]CTCTCTAGCCAGAGG | 90293 |
rs747233474 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117926999 | CAACCTCCGCCTCCC[A/G]GGTTCACGCCCTTCT | 90293 |
rs747245989 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050138 | CAGTCCTCCTGTCTC[A/G]GCCTCCCAAAGTGTT | 90293 |
rs747248023 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118060507 | AGCAGATGAAAAAAG[A/G]AGTATTATTTATAGA | 90293 |
rs747266927 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117953961 | AGAAAATAACTCAGA[A/T]GAAATTTGGGGAGAA | 90293 |
rs747282368 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118077279 | ATCAATTCTATAAGA[A/G]AAAGTTAAGCAGTAT | 90293 |
rs747286462 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117918187 | CATGCTGCCATAAAA[A/C]CCCTTAAAAGTAGCA | 90293 |
rs747289429 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080555 | CAAATCAAGACCACA[A/G]TGAGATACCCTCTTA | 90293 |
rs747294471 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100807 | TTATTTATACATTGC[C/G]TATATCTTGAATGTC | 90293 |
rs747310455 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081158 | AAAGCTACCTATTGG[A/G]TATTGTGCATGCTAC | 90293 |
rs747330254 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088127 | TTTAAGAGTAATACA[A/G]CAGACAGGGCAAAGT | 90293 |
rs747334457 | snp | A/G | 2.33762e-05 | 0.00341871 | intron-variant | KLHL13 | GRCh38.p7 | X:117901949 | CATTCTACTGTGGCT[A/G]TTAAAAAAAAAAAGA | 90293 |
rs747337922 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118051141 | CCACCAATATCATAT[G/T]CTATAAGTACTGGAA | 90293 |
rs747353860 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001131 | TGTTGTTTCTCATAC[A/G]TCACTGCAGACCTGT | 90293 |
rs747357801 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073106 | CTCAAAAAAAAAAAA[A/C]CCCCACAAATGAAGA | 90293 |
rs747358952 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950833 | AGAAGTGTCTGCTAG[A/C]AGCAGCATTTGCTAA | 90293 |
rs747364314 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967669 | TCTGAAAGTGACAGG[A/T]ACACTAGCTCTTTGT | 90293 |
rs747364501 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117979737 | ATGAAAAAATATGTA[A/G]AAACATACTATCTTA | 90293 |
rs747373543 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039594 | ACCAGGTAGATTCCT[A/G]AGGTTTCCGACTCTA | 90293 |
rs747376809 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019078 | ACATCTAAAATCTAC[C/T]TCCTTGGAAAATTTT | 90293 |
rs747382084 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118042180 | AACATATATGCACCC[A/G]ACACTGGAGCACCTA | 90293 |
rs747384960 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117941818 | TATTGAAGTGTTCCT[C/T]GTGTCTCTATCTCCT | 90293 |
rs747409646 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118016968 | TTCATTCATTCCCAC[C/T]GCCATCACCTTTGTT | 90293 |
rs747425865 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118051789 | TTGTGGAGAAGGTGG[A/T]CATTTTGTACGTTGA | 90293 |
rs747442024 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073764 | GTCCAGCTTACTTTT[G/T]TAACTTTTACTCACT | 90293 |
rs747452041 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117962612 | AACTTCACCACTTGA[C/T]AGTAAGCAAGTAAAG | 90293 |
rs747467884 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033696 | ACTAACGAGCAAAAT[A/C]ACCAGCTAACATCAT | 90293 |
rs747485791 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917867 | CAGTGTAAAGCAATG[G/T]TAAGAGTCTATAAGT | 90293 |
rs747491528 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898396 | ACAGATATGTCAAAA[A/G]TACTTTATGAAAAGA | 90293 |
rs747497318 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117965208 | CAGTCCCACCAACAG[C/T]GTAAAAGTGTTCCTA | 90293 |
rs747497337 | in-del | -/A | 0.224728 | 0.248719 | intron-variant | KLHL13 | GRCh38.p7 | X:118099122 | ATAATAATAAAATTT[-/A]AAAAAAATTATACTT | 90293 |
rs747504092 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117933444 | ATAAATGGTGCCAGG[A/G]AAACTGGATATCCAC | 90293 |
rs747508078 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942701 | ATATTCTTCCATCCC[G/T]TTATTTTGAGCCTAT | 90293 |
rs747514377 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108209 | TTTACTGAATAGACT[C/G]TAAAAGCACTTCACC | 90293 |
rs747527168 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117900219 | AGAAGTAAGCTAATC[A/T]TTAGTCAAATCATTC | 90293 |
rs747530851 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109915 | ACAGTGGCTCATGCC[C/T]GTAATCCCAATACTT | 90293 |
rs747540787 | snp | C/T | 2.30041e-05 | 0.00339139 | intron-variant | KLHL13 | GRCh38.p7 | X:117919486 | GGCTACATCAGAGTC[C/T]ACCACAGGAAAAATC | 90293 |
rs747551641 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118058335 | ACACACTAATTAATT[-/A]AAGTATGCCACACTA | 90293 |
rs747557399 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084463 | AAGATTCAAAAGATT[G/T]TAAGAAAGGTTGTGA | 90293 |
rs747566163 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118102961 | CTAAATTATGTGATA[C/T]TTTCTCATTCAGCAT | 90293 |
rs747583987 | in-del | -/TATC | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013188 | AATAAAGAAGGAAAA[-/TATC]TAATAGTTGGAATGA | 90293 |
rs747604791 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117977325 | ATTTAAGCAGTCACA[A/G]TATAAGAGAAAACGT | 90293 |
rs747609371 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048349 | ACATACACACAGATA[C/T]AGAAAAAGGACAAAA | 90293 |
rs747621170 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111357 | ACTATAAATACCCTA[C/T]GTCAGTTTAAGTCAG | 90293 |
rs747646634 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056306 | TTGCTGAAAAACAGA[A/G]TAAGATCTAAATAAA | 90293 |
rs747649034 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000218 | CAAACAAATGCAGCC[G/T]GGAGGACTTGTCAAG | 90293 |
rs747664399 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118028397 | AGGAAAGACGTTATA[C/T]AAGTTAAACTATTTC | 90293 |
rs747675672 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013756 | GAAGTCAGAGACCCC[A/G]AACGGAGAGACCGGC | 90293 |
rs747684122 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913085 | GAAATTAAAGAAGCA[A/C]AGTCTACAGTAATAA | 90293 |
rs747685277 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985445 | AACAGGCTTTATATA[G/T]TTAAAAAAAAAAAAA | 90293 |
rs747690722 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030397 | TGTTGAAAAGGGAAA[A/T]ATCTATATCTAGATT | 90293 |
rs747705600 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102307 | GTTCTTCCCGGCTCA[C/T]ATAGTAATAATTATT | 90293 |
rs747714786 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118103114 | ATACATATATGCCAG[A/G]ATTTCTAAATCGAGC | 90293 |
rs747715127 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956208 | GGATTCATTTGGGCA[A/G]AATATTTATGTGTCA | 90293 |
rs747734771 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118078199 | TATTTCATAATCACA[A/G]ATGGTGGTCCAATTT | 90293 |
rs747735991 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118047057 | ACTCTGGGGTAAAGA[C/T]GGCCTTTCAAACAAG | 90293 |
rs747738318 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975542 | ATTACATGCACCTGC[C/G]ACCATGCCTGGCTAA | 90293 |
rs747738439 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117997567 | TAAGAATATAAGGAT[A/G]AATGTAAAGATTCAA | 90293 |
rs747743400 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118047780 | GGGAGAGATGTTTAC[C/T]TTTAATCCTGTATTT | 90293 |
rs747750158 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117946387 | ATAAGTAAGAATAGG[A/G]GAACCTTAGTCAGTA | 90293 |
rs747770950 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117914993 | ATGGATGGCCGACCA[C/T]AAGCAACGGGGATGG | 90293 |
rs747771981 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928727 | ATCAGTCAATGACTA[C/T]ATTAAAAAAGAAGAA | 90293 |
rs747778518 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118022702 | TTGGTGTGTTTCTTT[C/T]CTACTGAGTTATGTA | 90293 |
rs747784027 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977022 | AAGAGAAACTAGAAA[C/T]CAAATTTCAATCTCC | 90293 |
rs747799321 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926426 | CCTCAAGGATTCCAG[C/G]GAGTAATGATAAACA | 90293 |
rs747803777 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938902 | TATAACAAACAAAAA[G/T]AGCCGAAGACTCGTT | 90293 |
rs747810594 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998758 | CTCTGGGGGCACCAT[A/G]AGAAGCTACTGACCA | 90293 |
rs747812365 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911116 | TATACAAACAGACAC[A/T]GATCACAGGCAAAAG | 90293 |
rs747823043 | snp | A/T | 9.2953e-05 | 0.00681673 | missense | KLHL13 | GRCh38.p7 | X:117945543 | CCTCCAAGGGACAAT[A/T]TCATGTGTTGGTCTT | 90293 |
rs747832787 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967272 | ACCGCCTTTCTCAAA[G/T]TCTTGAGGATATAAA | 90293 |
rs747847328 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117939392 | GTGAACAGTGCTGCA[A/G]TAAACATACCTGTGC | 90293 |
rs747850281 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096365 | ACACATACACCCTCC[C/T]ACGACTAAACCAGGA | 90293 |
rs747863215 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049592 | GAGTGGTGATTCTTC[-/A]CTACAGTAAATCTAA | 90293 |
rs747865766 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118062067 | TATTTCTCATCACCT[A/G]GAGAAGAATTTGGTC | 90293 |
rs747875698 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118039436 | TTGAGTGAACATCAC[C/T]GGTAGCTAGATAGTA | 90293 |
rs747885656 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967934 | GGACAGTGTGAATCC[C/T]ATAATTAAAAAAAAT | 90293 |
rs747894190 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118061634 | GCATTTCTAATTATA[C/T]ATTTGTTGAAAAGAG | 90293 |
rs747895855 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083287 | ACCTATGCCCTCGTG[C/T]TTACTGCAGCACTAT | 90293 |
rs747908849 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040956 | TTACACTAGAGTAGT[A/G]TATCTGGCAAAAATA | 90293 |
rs747910721 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117929725 | GGCAGGAGGATTGCT[C/T]GAGCCCAGCTGTTTG | 90293 |
rs747921676 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907400 | TTAACAGGGGTGATA[A/C]TATCAACAAGCAAGG | 90293 |
rs747931845 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089636 | AGAAAGAAAGAAAGA[-/AA]GAAAGAAAGAAAGAA | 90293 |
rs747948925 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118096781 | GGTTCAATATACGCA[A/G]ATCAATAAACGTAAT | 90293 |
rs748000745 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961334 | GATTAATAAATATGG[C/T]TTAGTTACAGGAATG | 90293 |
rs748001127 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117399 | CAACATTAAGAAAGA[A/G]GAAGGATAAAAACTA | 90293 |
rs748040000 | in-del | -/TA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064176 | ATTACATAAAGCATT[-/TA]TGTTACAAAATTTGT | 90293 |
rs748042882 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118090442 | AGAAAAAACAAACAA[A/C]CAACCCCATCAAAAA | 90293 |
rs748043860 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107551 | AATAATAAGTATAGT[C/T]ATATTTCATATGTGG | 90293 |
rs748047906 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033031 | TGAAGTGAGAAGGGA[A/C]GTTTAGAGAAAAAAG | 90293 |
rs748069565 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991334 | GCCAAGGAGAGAGAT[A/G]CTAACAATTAAAGGT | 90293 |
rs748078141 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957877 | AACAGCATGCAAAAA[C/T]AAGTCAAATAACTCT | 90293 |
rs748090372 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104456 | CACTCATACTAGTGG[A/G]TTTAGCAGTTTTGTT | 90293 |
rs748093167 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118028035 | GATTTTTAAATAATA[A/T]AAATATATACAATCA | 90293 |
rs748094869 | snp | C/T | 2.29808e-05 | 0.00338967 | missense | KLHL13 | GRCh38.p7 | X:117909417 | ATCCATTTATTGTAT[C/T]GAGGATCAAATCTGA | 90293 |
rs748098319 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981740 | GGGTTTCTAGAAATA[C/T]CAATTTTTCAGATTC | 90293 |
rs748110323 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052697 | AAAAAATTAGCTGGG[C/T]GCACCTGTAATCGCA | 90293 |
rs748114970 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117930660 | CCTAAAAAGGGAAAG[C/T]GGCAGACAGTCTTCC | 90293 |
rs748135846 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911143 | AAAGACTTAAATGTT[C/T]GGTTGTTTTTAAAAT | 90293 |
rs748150879 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029491 | ACTATATCTAAAATA[C/T]CTACATTTTAGTAAT | 90293 |
rs748170074 | snp | A/C | | | missense | KLHL13 | GRCh38.p7 | X:117910072 | TGGCAATCCGTCCAA[A/C]TTCAACACAGTTGTC | 90293 |
rs748181182 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093978 | TAATTTCTGCATTTC[C/G]AACTGAGGAACGCAG | 90293 |
rs748198305 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118053291 | GTGGCACATATACAC[C/T]ACGGAATACTATGCA | 90293 |
rs748202266 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094271 | TAGCCGATGCGATCA[A/C]ATGGAAGAAAGGGTA | 90293 |
rs748203811 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023866 | TGTGAGCCTTTTCCT[A/G]TGTTTTACTGTATTT | 90293 |
rs748211470 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117972239 | TCAAACATATTAATA[C/T]TCATACACAACTAAA | 90293 |
rs748213585 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117949210 | ACAAGATATACTCTC[A/C]AAATTGCTAGTGCAA | 90293 |
rs748218788 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117943609 | ATCCTTTCTTCTGCT[A/T]GATTGATTTGGCTAT | 90293 |
rs748243148 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117936347 | GTATCAAATGACTTT[A/C]TAGGAATTTTCTTTG | 90293 |
rs748258444 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911905 | ATATTTTTAAAATAC[C/G]TAACACATAACTGTA | 90293 |
rs748261153 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902970 | CTTTGGTCCACCATA[A/T]GATATAGTTCTGGGC | 90293 |
rs748273522 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118003165 | GTTCCTAACCCTAAA[A/T]AACCAGGAATAGGTT | 90293 |
rs748288121 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044860 | ATACCTGATAAGCAC[A/G]GACAACCAAAGCAAA | 90293 |
rs748305341 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970577 | AGTGGAATTATGCTA[C/T]ACTTAAGTATCATTT | 90293 |
rs748327565 | in-del | -/TT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076332 | TCACAAGATAAATTA[-/TT]ATACACAATTGGGAT | 90293 |
rs748327768 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117995851 | TACTTCTAATATACT[A/G]TATGGCTGAGTATTC | 90293 |
rs748351665 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021296 | GCACAATGTGCAGGT[C/T]AGTTACATATGTATA | 90293 |
rs748353220 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923199 | ACTTAGCTGTCTAAG[C/T]ATATCTGTGGGAGAT | 90293 |
rs748357024 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118094866 | GTCACCACCAGGCCT[A/G]CCCTAAAAGAGCTCC | 90293 |
rs748359839 | snp | A/C | 2.29877e-05 | 0.00339018 | intron-variant | KLHL13 | GRCh38.p7 | X:117920403 | GTTGAGTCACTAATC[A/C]AGGTAAAATGAGGTT | 90293 |
rs748372822 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118058554 | CTGGGTCAATAACTA[C/T]AGCTCAGTTATGCAA | 90293 |
rs748374557 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111954 | TAGCTAATTCATGTA[A/G]TCTTTGCAAGTACCA | 90293 |
rs748379537 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118112807 | CAAGGAAGGGCTTAG[A/G]GCAATAAATTCATTT | 90293 |
rs748398229 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114445 | CTGGCAAATATAAAT[A/G]GTCTTACTATGCAAT | 90293 |
rs748407451 | in-del | -/AAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013173 | AGGGGATAGAAAATA[-/AAT]AAAGAAGGAAAATAT | 90293 |
rs748407889 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118037638 | TTGGGAGATACACCT[A/C]ATGCTAGATGACGAG | 90293 |
rs748418745 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007225 | AGCCAGCCTGGTGAA[C/T]ATAGCGAGACCCCAT | 90293 |
rs748429433 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906413 | ATTCTTTGGGAGCAA[C/T]AGTAATCAAGGCAGG | 90293 |
rs748435009 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092977 | CAGGCTACTTCCTAA[G/T]AGTGAAAAAATTTTA | 90293 |
rs748443100 | snp | A/G | 2.28191e-05 | 0.00337772 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899142 | AGCGACCCCAACATC[A/G]CTCTGCCCTCTTAAC | 90293 |
rs748449170 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118087803 | TGATTCTTCCCTCAC[C/T]GTACCAGCTAATGGA | 90293 |
rs748462796 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118059394 | TCACTTTTCTTCTCA[C/T]GCTGTTTCCACTACA | 90293 |
rs748482537 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958228 | TTCCATATACACTAC[A/G]TTTTATTCCTATACA | 90293 |
rs748490827 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118031900 | CACCGTGCGCGAGCC[A/G]AAGCAGGGCAAGACA | 90293 |
rs748492805 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057546 | TGAAAAATCGGCCGG[A/G]GCCGTGGCTCATGCT | 90293 |
rs748500103 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118049946 | AGCAATCTGCCCATG[C/T]CACCACCATGTGGTC | 90293 |
rs748503668 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117988224 | TTGCAAAGGCAGAAA[A/G]GGAGGAGGGGTAACT | 90293 |
rs748506396 | in-del | -/A | 0.182749 | 0.240785 | intron-variant | KLHL13 | GRCh38.p7 | X:117978845 | TATTCCCATCTGTTT[-/A]AAAAAAAAAATGCTT | 90293 |
rs748506728 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007912 | GTAGATCTTCCAGGG[A/G]AAAAAGGTATTAATC | 90293 |
rs748510892 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118079752 | ACGTTATTCTTATGA[A/C]ACTACCAACATTATT | 90293 |
rs748515994 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038516 | AGATTGCAGTAATGG[C/G]GACTTTCCATTGGAA | 90293 |
rs748517965 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014038 | AAATTGATTGTAAAA[C/T]ATGTGTGTTTGAACA | 90293 |
rs748521224 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117984011 | ATATTACAAGCTTTC[A/G]GAGAACAGATGGCTA | 90293 |
rs748536886 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117917670 | TTTTTTGTATTGTGT[A/T]TTATCCAGTTTGGTC | 90293 |
rs748538812 | in-del | -/TCA | 2.28227e-05 | 0.00337799 | cds-indel | KLHL13 | GRCh38.p7 | X:117909576 | CACTCATGGGCCTTT[-/TCA]TCATACATGCGCAAT | 90293 |
rs748540527 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118024329 | TTTTGGAAGAAAACC[C/T]CAAATTTGGAAGAGC | 90293 |
rs748547423 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926975 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAACCTC | 90293 |
rs748563592 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117934055 | ACTAAAATATCTATA[A/T]GTTCTCACTTATAAG | 90293 |
rs748570248 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969347 | ATTTGCCTGAAGGAA[A/C/T]CATTTGCTGTTTTAA | 90293 |
rs748572423 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117916958 | TCCTTTAAAAAATAT[A/G]GTATCTTGAGATGTT | 90293 |
rs748587867 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041405 | GGTGGTGCATGCCTA[C/T]AGTCCCAGCTACTAG | 90293 |
rs748595936 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955321 | TTAAGAGAATGTTTA[-/T]TTATCTTTTAAGGGG | 90293 |
rs748602883 | in-del | -/A | 0.0804534 | 0.183722 | intron-variant | KLHL13 | GRCh38.p7 | X:118080407 | ATCTATAAGTAACTT[-/A]AAACAAATCAACCAG | 90293 |
rs748605929 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097569 | TCTTCACAGAATGGG[-/A]AAAAAACTACTTTAA | 90293 |
rs748612790 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004347 | AGCAATACTGGAATA[C/G]CAATGAGCACTCCTA | 90293 |
rs748612851 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117982369 | TAGACACAAACCTTT[A/C]TAAAATACGTCAAAG | 90293 |
rs748613511 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917751 | GTACTAAACTTCTGC[A/C]TTAGAGGATAGGCCA | 90293 |
rs748618657 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916388 | ATCCTTCTGTATTCA[C/T]TTCATTGTCCTCTTT | 90293 |
rs748623911 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117908380 | GTATTTCTCCTAATG[C/T]TATCCCTCCCCTAGC | 90293 |
rs748624165 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941124 | ATACTTTACATCAAT[A/G]CCTAGTTTATTGAGA | 90293 |
rs748630426 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025278 | GGTTTCAGTTACCCA[A/T]GGTCAACCACATTCT | 90293 |
rs748641271 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118055783 | AATAATAATTTAATG[C/T]AATATTTTTAAAAGT | 90293 |
rs748663349 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117908929 | TTGTAACCTGTTCAG[C/T]AAAATATCATATGGC | 90293 |
rs748676915 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118051089 | AGAGGCCCATTACAA[A/G]AATGTCAGGTCCATG | 90293 |
rs748688477 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073062 | CTGTGCCACTGCACT[A/G]TCACCTGGGTTACAG | 90293 |
rs748693806 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118091545 | ATGGAAAAGACAGAG[A/G]AAAAATCAGTGAACT | 90293 |
rs748737544 | in-del | -/CT | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118033404 | ATCTCTCGGCAGAAA[-/CT]CTACAAGCCAGGAGA | 90293 |
rs748746809 | snp | C/G | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117631 | GTGTGATTCTGGTAC[C/G]CAGGCTCTTAACCAC | 90293 |
rs748752208 | snp | C/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:117962982 | AAATAAATTGTATTA[C/T]ATTTAACTATGCTAA | 90293 |
rs748758781 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118853 | ATTAAGTTAGTGCTC[C/T]GAGAGTGTTTTCCCA | 90293 |
rs748759716 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922568 | ACTGGAAACCAGGAA[C/T]TTATTTGTGAAACCT | 90293 |
rs748768760 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118042032 | GATATTCCATGCAAA[C/T]GGAAACCAAAAAAAG | 90293 |
rs748771687 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974467 | TTTCCAAATTATTCC[C/T]AGTTTTTAAAGATTG | 90293 |
rs748776614 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073700 | AGGGATGTTTGGAAA[A/G]GAATGGTTAAACTTT | 90293 |
rs748791783 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092253 | ATTGACTCTAAACCA[C/T]ATCATAATCAAACTT | 90293 |
rs748793994 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117982903 | ATCCATTATCTTGCC[C/T]TCCCACACTCCAGAT | 90293 |
rs748803353 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118065444 | ACTACCTTTGGGCCA[C/T]GCTGATTAGACCAGA | 90293 |
rs748808498 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118066373 | ACTAACAATCCCATG[A/C]TTCCAAAATACCAAC | 90293 |
rs748819249 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046488 | TTGATAGCACAACAG[C/G]AGCAACTATAGTTAA | 90293 |
rs748835128 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084357 | GATTTTATTAGCTGA[A/C]TAATAGTGACAAACT | 90293 |
rs748840511 | in-del | -/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118012671 | AAAATGTGGCCATCC[-/G]TGGGCGGGGGCGGGG | 90293 |
rs748849648 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013104 | GTGCTGCGATTAAAG[A/C]AGTAAACAAGTTGAA | 90293 |
rs748851390 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967415 | CTTTCTCATCGCTCC[A/G]TCTCCCCAAGTTTGG | 90293 |
rs748854875 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117997075 | TTTCGGGAAGACTCA[C/T]ACTCACTTGCACTTT | 90293 |
rs748865711 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109332 | ATCATGGGAATTTAC[A/G]GCTATGAAAATGTTT | 90293 |
rs748876653 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117963820 | TCTCTGATGGCCAGT[A/G]ATGATGAGCATTACA | 90293 |
rs748889831 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117983681 | CCTGAACAGTTAAAA[C/T]CACACATAACAATTT | 90293 |
rs748891942 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117899704 | TATATTTTGATCACT[G/T]ATAGAGTTGGGTCTG | 90293 |
rs748906652 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056097 | TGATGGAAGACTATT[A/G]GAAGTAAAAAAATGA | 90293 |
rs748924578 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060625 | ACAGATTAAAAAAAA[-/G]CAGAGGCTTCTCAGA | 90293 |
rs748925369 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077310 | GCAGTGGGAATCTAC[-/A]AAAAGTAATTACTTC | 90293 |
rs748929801 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955477 | TACCAAATCTCAGTC[C/T]TGATTTTTGTAATGG | 90293 |
rs748932228 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942989 | TTTCCATATTTAGTG[C/T]TTCCTTCAGGAGCTC | 90293 |
rs748937699 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087592 | TAAAAGAGTCTGGAA[A/G]TAAGATTTCTGACTT | 90293 |
rs748943184 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975024 | AAATATATTTAAAAG[C/T]TTTTTTTAACCTGCC | 90293 |
rs748949594 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118021917 | GTTTCCTGACTTTAA[A/T]GATCGCCATTCTAAC | 90293 |
rs748991105 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118067224 | GTATTTGTGTATCTA[A/G]GCATATCTAAACTTA | 90293 |
rs748996204 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015728 | TTATAGGAACAAATA[C/T]GGTGATAAATTTCAT | 90293 |
rs748998851 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080691 | CTCAGCCACTGTGGA[A/C]AGCAGTTTGGAGATT | 90293 |
rs749001230 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913884 | CAAAAAAGGATAAAA[C/T]TCTTCAAGCACCTGT | 90293 |
rs749003544 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030256 | GGTTAAATGAAATTA[A/G]TATTTTACACACTCT | 90293 |
rs749008249 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117958054 | TCATGGTATTTCTCA[-/G]CAACAATGAACAGAA | 90293 |
rs749041172 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118046941 | CCAAGAGCAGTTTCA[A/G]TATCAGTGGGGAGAA | 90293 |
rs749051853 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938864 | GCTTTTTTTTGAGCA[C/T]CTTAAAAATCTATCC | 90293 |
rs749054006 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059906 | GAACTGTGTTACCGT[A/G]AGCACTTAACTACCG | 90293 |
rs749061648 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118006139 | ATCAATACTTACTTT[A/C]TATCCAACCCACAGA | 90293 |
rs749067854 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975390 | CAGCTTATGAATCTT[C/T]TTGTTTGTTTGCTTT | 90293 |
rs749070260 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008110 | TTATTTCATGGGTCC[A/G]TATTCCTGGTCACAT | 90293 |
rs749082000 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117956680 | TCACACCCCAAACTA[C/T]AATTTCTGACTCTCA | 90293 |
rs749088534 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078108 | TGAACCTCATTCAAA[A/G]TATTTAATTAGTAGA | 90293 |
rs749105050 | snp | G/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118095787 | AACCTGCTCCTGAAT[G/T]ACTACTGGGTACATA | 90293 |
rs749125452 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081899 | TCCATGATACTACAA[A/G]TGACAGGATTTAATT | 90293 |
rs749130623 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118096298 | AGAGAATACTATAAA[A/C]ACCTCTACACAAATA | 90293 |
rs749131042 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117914796 | AATGCAGTTCCTTTA[C/T]TGAATGCAATGTTAG | 90293 |
rs749137095 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938414 | CTTAAAACTATGTTC[C/T]TTGATCTGCAGCATC | 90293 |
rs749157840 | in-del | -/TTAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908067 | TCAACTACAAGGACA[-/TTAT]TTATTTATTTATTTA | 90293 |
rs749165926 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070841 | TACATGTGACATGCT[A/G]GTGCACTGCACCCAC | 90293 |
rs749171664 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954345 | TTATTTCTCATTCTC[C/T]ACATTTCTTATATTT | 90293 |
rs749183593 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117906300 | GCAAAAACAATGGGT[A/C]CAAGAAAACTGGAAA | 90293 |
rs749186357 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117976890 | TAAAAGGAGAAGATT[G/T]GTTGAAATTTTAGGA | 90293 |
rs749191970 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117989079 | CAGACATAGAGGGTT[-/A]ATGAGGAAGTAAGAA | 90293 |
rs749195307 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910767 | TATATCTACAACAAA[A/T]CTCTCATGTAAATGA | 90293 |
rs749200544 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016934 | ATTCATCCCTAAGTA[C/T]TTCACAAATGCATTC | 90293 |
rs749209852 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117928383 | ACAGAATACTTCACC[A/G/T]AAGAACAGTAGGATG | 90293 |
rs749222060 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039385 | GACTCAGGACAGGCA[G/T]CATTCACCACAAGCT | 90293 |
rs749223809 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089796 | AAAAAAGTATCAATA[C/G]GGCTGGGTGTGGTGG | 90293 |
rs749241392 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032443 | TGACCCCTGACCCCC[A/G]AGCAGCCTAACTGGG | 90293 |
rs749243697 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939195 | AACATCTGGTGTTTG[G/T]TTTTCTTTTCTTGTG | 90293 |
rs749245693 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117990319 | GACTGCTGAACTGAA[-/C]TGAGTAAGGAAAACA | 90293 |
rs749246655 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117912788 | TAGTTGGTATATATA[C/T]TTATGGGGTACCCAA | 90293 |
rs749255675 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117980031 | AAGAATATGGCTCTA[C/T]TGAATGAAAATACAT | 90293 |
rs749268598 | snp | A/G | 2.4335e-05 | 0.00348811 | missense | KLHL13 | GRCh38.p7 | X:117898913 | AGAGATGATCTTAAG[A/G]TGCAGAAAGAGGGGA | 90293 |
rs749272816 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118032737 | CGGAACAAAGCTGGA[C/T]GGAGAATGACTTTGA | 90293 |
rs749274893 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118052084 | TCATGAATGTGGCAA[C/T]TGAAATCAGTAGGAA | 90293 |
rs749277532 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118102763 | GATGGACCTAACCTA[C/T]ATGCAGAGTCATTCT | 90293 |
rs749284846 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112594 | AAAATCAGTTTAAAC[C/T]AATAGAGATTTGTGA | 90293 |
rs749289352 | snp | A/G | 2.50991e-05 | 0.00354245 | intron-variant | KLHL13 | GRCh38.p7 | X:117899435 | GAAGTAAATAATTAT[A/G]GAAATGCAAAAGTAA | 90293 |
rs749304366 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048206 | GTTAATGTTTTGTTT[A/T]ATTTTGTTTTCATAA | 90293 |
rs749313132 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026588 | TGCCCCCAAAGAAAT[A/C]AGCAGTTTACAAATG | 90293 |
rs749318671 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117951712 | TTTAAAATAGAACAG[C/T]ATTAATAAATAGCTT | 90293 |
rs749321959 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117980812 | GACCAAATAATGAAT[A/G]AGAAAATCTTACACT | 90293 |
rs749325229 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118091961 | TAACTCAGGAATGGA[A/G]AACCACCAAACATCA | 90293 |
rs749336141 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099326 | ATAACTTAAAACTTC[A/C]TTAAACTGAAAATTT | 90293 |
rs749358148 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040769 | GGCATTTAATTATCA[A/G]ACTCCCAAAGGTCAA | 90293 |
rs749363546 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043231 | TAACAAGTAATGAGA[C/T]TGCAACTGTAATAAA | 90293 |
rs749368875 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968965 | ACATTACAGAGGCAA[C/T]TGCTATAGAATGTTG | 90293 |
rs749417446 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052644 | CAGCCTGGCCAACAT[C/G]GTGAAACCCCGTCTC | 90293 |
rs749419678 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970288 | CAATACTGATGCTAC[A/G]CAAGCATACGTACAA | 90293 |
rs749437815 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117952169 | TACTACAAGACTACA[A/G]TAATCAAAACAGCAT | 90293 |
rs749439875 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942777 | ATGGGCCTTGTCTAT[C/T]CAATTTGCCAGTCTG | 90293 |
rs749446326 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118082812 | TTTCATTTTTCTGCA[C/T]ATGGATATCCTATTT | 90293 |
rs749454592 | snp | A/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987357 | ATAGAAGGTTTAGAA[A/T]CTCCAAGGGTGAGCT | 90293 |
rs749472723 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939404 | GCAATAAACATACCT[A/G]TGCATGTGTCTTAAC | 90293 |
rs749475068 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118002594 | GTGAAACTCTGTCTC[A/G]AAAATAAATAAATAA | 90293 |
rs749477669 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099679 | AAAAATTAGCTGGGC[A/T]TGGTGGCACACACTT | 90293 |
rs749496819 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020365 | TGAGACTTTGCTGAA[C/G]TTGCGTATCAGCTTA | 90293 |
rs749512295 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043810 | GGGAAAAAACTGAAA[G/T]CCTTTCTTCTAAGAT | 90293 |
rs749535242 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117901736 | TCTCAAACTCCTGAC[A/G]CCTGAATTATTATTA | 90293 |
rs749537115 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921497 | CATTTTGGCAAGATT[A/G]AGTCTGTAGTTTCAA | 90293 |
rs749542959 | in-del | -/ATAAAAA | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:117994891 | TGAGACTTCATCTGT[-/ATAAAAA]ATAAAAAATAAAAAT | 90293 |
rs749544552 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117964634 | GGTACATGTGCACAA[C/T]GTGCAGCTTTGTTAC | 90293 |
rs749558619 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916179 | ACAAAACAAACAAAC[-/A]AAAAAAAAAACACTA | 90293 |
rs749562686 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093942 | TCTACAGCTCCCAAC[A/G]TGAGCGACACAGAAG | 90293 |
rs749586101 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911800 | TATCCAGTCTATCAT[C/T]GATTTATTACTCAAA | 90293 |
rs749588289 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118068336 | GCAAAACAACAAATA[A/C]ACAGCTATATTTTAA | 90293 |
rs749591057 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039926 | GTTTGGGGGAAATTA[A/G]GGGAAGAGAACAAGG | 90293 |
rs749597951 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117964978 | ACATTTTCTTAATCC[A/G]GTCTATCATTGATGG | 90293 |
rs749607984 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076621 | ACCATTATTCTAGAC[A/G]TTTCTGAGTAAAGCA | 90293 |
rs749608256 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013727 | CTACTACAACTAATA[-/C]CCCCATGTTGCAGGA | 90293 |
rs749623372 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936112 | GACAACCTGGAATAA[C/T]AGGGAGAAGTGAAAG | 90293 |
rs749628023 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118111890 | GAGTGAGAGAGCGAG[-/A]CTCCGTCTAAAAAAA | 90293 |
rs749631677 | in-del | -/A | 0.00281987 | 0.0374431 | intron-variant | KLHL13 | GRCh38.p7 | X:117901952 | TCTACTGTGGCTGTT[-/A]AAAAAAAAAAGAAAA | 90293 |
rs749633601 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118002330 | GGCCAGGCGCGGTGG[C/T]TCACACCTGTAATCC | 90293 |
rs749633985 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036579 | CTTCCTTATACCTTA[C/T]ACAAAAATCAATTCA | 90293 |
rs749666267 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987037 | AGGAACAAACATGAA[C/T]TGTGAAGAGAGATGG | 90293 |
rs749670586 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029756 | AGCAGATTGCTTCAG[C/T]CCAGGAGTTTGAGAC | 90293 |
rs749676853 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117925236 | CATTGATACTGTCAG[G/T]TATTTAAAAGGAATT | 90293 |
rs749683883 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014482 | AGACAATGCATGCAC[A/G]GCGGCACACAGACCC | 90293 |
rs749687128 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981737 | TAGGGGTTTCTAGAA[A/G]TATCAATTTTTCAGA | 90293 |
rs749717068 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118007079 | TTCTAAGTGACCTCC[C/T]ACTGATTTGAGTAGC | 90293 |
rs749717984 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933940 | TCATATACACCATGG[A/T]ATACTATACAGCCAT | 90293 |
rs749720374 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117957063 | GCTCTCACCAAAATT[A/G]TTTGACCACCTTTGA | 90293 |
rs749721084 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117977362 | TTGCCAATACTCTGA[-/T]TTTTTTTTCTCAATG | 90293 |
rs749728849 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915274 | TAATTTAGTAACAGA[A/G]GCAAAGCAAAAGGAA | 90293 |
rs749731691 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023499 | CATTCTATGAATAAC[C/T]TTCACGATCTTAAAC | 90293 |
rs749739999 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117948495 | CTCATGTAAGAATAA[C/T]AATTTCCTAAATCTG | 90293 |
rs749745245 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086570 | ATAAGGTAGGTATTT[A/G]TGTCCTGATATAGAA | 90293 |
rs749747965 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092861 | TGGGGAAACTGGGTG[A/G]CAGGTACCCAGGACC | 90293 |
rs749752225 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117925939 | ACCGCCACCTGTCTC[A/G]GCCTCCCAAAATGCT | 90293 |
rs749759139 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118104087 | AAATGCCAGGCATGG[G/T]GATGTGCGCCTGTGT | 90293 |
rs749762064 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117932132 | AATGAACAAATCAGG[G/T]TAATTATTATATCCA | 90293 |
rs749787767 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117916280 | GGTATGACTAAACAA[A/T]GGCAATTTTCCATTA | 90293 |
rs749818662 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000751 | TGACCTGAACTGACA[C/T]GAGGCTATTCACAGG | 90293 |
rs749822843 | in-del | -/A | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:118048707 | AAAGAGCTTTCAAAG[-/A]AATAAAACCAGACAG | 90293 |
rs749839743 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907691 | ACTGCTTTTAAAAGT[C/T]CAATTATTAAAATAT | 90293 |
rs749843391 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117968206 | GGCTGCATTGGGAAC[A/G]GGAGAGAAAAGATAC | 90293 |
rs749843871 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104846 | TCAGCTCTGTGAGTA[C/T]ACTAAACATTACTGA | 90293 |
rs749845504 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117978277 | ACACTCATGTATATG[C/G]GTAGAGAATTCCTCA | 90293 |
rs749846027 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096866 | AGAAAAGGCCTTTGA[C/T]AAAATTCAGCAACGC | 90293 |
rs749846692 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007811 | AGAATCATAGTATGC[C/T]TATCTGTGGATCACA | 90293 |
rs749859382 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060106 | AAAACAGACATAACA[C/G]AGCATATAAATGCTA | 90293 |
rs749867842 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022530 | CTGATAATGGCCAAC[C/G]TAATAGGTGCAAGGT | 90293 |
rs749874687 | snp | C/T | 0.000316932 | 0.0125843 | missense, intron-variant | KLHL13 | GRCh38.p7 | X:118028424 | TTTCCATAAATATAC[C/T]GGTTACGAAGTATTG | 90293 |
rs749879869 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080272 | ACAAAATTTGACAAA[C/T]GAGACCTAATTAAAC | 90293 |
rs749882496 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109215 | CTGTAAGAACTCAAC[A/C]CATGTTTAGATTTAG | 90293 |
rs749899622 | snp | A/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:117959087 | GTACTGCACATCATT[A/T]AAAAAAAACACTCTA | 90293 |
rs749934420 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118105140 | AAATATTCAGAAATA[C/T]GTTCCTTGCTTTTCA | 90293 |
rs749934999 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927271 | CTCGCCTCGCCCCGC[C/T]CCGCCCCTCCCGGCC | 90293 |
rs749936291 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025220 | ACCCTAGCCCAGATG[A/T]TAGTACAGTAGTCCC | 90293 |
rs749937742 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978749 | TTCTTGCCCTTCCTT[A/C]TTCATTTTGTTTTCT | 90293 |
rs749939895 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985586 | TATATCTTGAACTTA[A/G]TTCTGGTAAACTGAA | 90293 |
rs749948304 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118114192 | CAAACAATTTGAAAA[C/T]TGGTCAGTCTCATTT | 90293 |
rs749972130 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118110791 | TAACTGAATTTCTTA[C/T]CCCCACCCCCACAAA | 90293 |
rs749977702 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117983631 | CATACCCTGACAGCA[A/T]TTTAGCTGTAAATTA | 90293 |
rs749987869 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117918818 | GTATTAGTTCTTCTT[A/C]AGATCTAGCTCCCTT | 90293 |
rs749990971 | snp | A/C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118061281 | TGGGGTACTTTTACC[A/C/G]CTCAAAATTATTGAG | 90293 |
rs750012643 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935971 | CATTGATTTGCACAA[C/T]AAATGGGTGAATTAT | 90293 |
rs750020215 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118097879 | CTGGCTAGCCATATG[G/T]AGAAAGCTGAAACTG | 90293 |
rs750030210 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008948 | AGTACAAAGTAACGC[C/T]ATTTAAGTGTTAGCT | 90293 |
rs750031705 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005403 | TAGTTGACATAGATA[G/T]AGGGTGTGGTAGGCA | 90293 |
rs750041278 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941643 | GTGTTTGTAGTATTC[C/T]CTGATGGTAGTTTCT | 90293 |
rs750073989 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117951229 | GTAAACTAATGTATA[C/T]AAAATAAGCCTGGCA | 90293 |
rs750083941 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117992793 | TCTTTCAGCAGTTAC[C/T]ATACAATGTTCATAG | 90293 |
rs750092865 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041880 | ACAACATTGAATCTA[C/T]GTGACTAAATCCTAC | 90293 |
rs750099373 | in-del | -/AAATCCTG | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001530 | TGAGTATACAAGGCT[-/AAATCCTG]ATTGTCAGAACACTG | 90293 |
rs750107628 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073355 | GCAGGGAAACTCCCC[-/T]TTATATAACATCAGA | 90293 |
rs750108645 | snp | G/T | 0.0860103 | 0.188699 | intron-variant | KLHL13 | GRCh38.p7 | X:118098440 | ACAGGTGCTGGAGAG[G/T]ATGTGGAGAAATAGG | 90293 |
rs750121797 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117937628 | TCCCTAGTGTTTCCA[C/T]ACCATTTGCTATGCA | 90293 |
rs750123593 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917495 | AATTGTTAAACAATT[A/C]TAATAAATGTTTCAA | 90293 |
rs750147411 | snp | C/T | 2.28185e-05 | 0.00337768 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909635 | CAGCACTCCTCCTAG[C/T]GTAACCAAGTGAGTG | 90293 |
rs750171473 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118019916 | TAGTATAGTTTGAAG[-/T]CAGGTAGTGTGATGC | 90293 |
rs750174381 | in-del | -/A | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117971459 | GACAAACAGTTTTTG[-/A]AAAACAAATATAGCT | 90293 |
rs750182307 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118066021 | AAAAACCAAGTAGAA[C/T]TGTTACAAAGCAGAC | 90293 |
rs750198396 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117910225 | AGATACAAATAGGAT[C/T]CTTATCTAAATGTAT | 90293 |
rs750208881 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117993672 | GGACTTCCAAGTTAC[C/T]GAGAGAGAAAAAGGT | 90293 |
rs750219853 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012960 | ATTAGTATTGACTCA[C/T]GGATAAAAATCAGAG | 90293 |
rs750245388 | snp | A/G | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117964099 | CTAATGCTAGATGAC[A/G]CGTTAGTGGGTGCAG | 90293 |
rs750251227 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085153 | CAACCGATAAATGAA[A/T]AAACATAAGTAGTAG | 90293 |
rs750257443 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118013672 | GCAAAAATCAATAAA[C/T]AGAAGGAAAAAAGAT | 90293 |
rs750264717 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117934093 | TAAACATTGGGTACA[A/C]ATGGACACAAAAATG | 90293 |
rs750265190 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047714 | GTGCATGCACATGCA[C/T]AACACATAAAGCCTG | 90293 |
rs750269931 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118066954 | CTTCCCATTGGTATA[C/T]ACATAGAGAGTTTCC | 90293 |
rs750280029 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968205 | AGGCTGCATTGGGAA[C/T]GGGAGAGAAAAGATA | 90293 |
rs750283302 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998505 | ACAAGAATCAAAGAA[A/T]CACAGATATCAGGAG | 90293 |
rs750284485 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928660 | AACTAAATGAAAATA[C/T]AACATCAAAAATTGT | 90293 |
rs750291470 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955245 | GTGGTGAAAATCCTA[C/T]CCTTTCCTGAATTTC | 90293 |
rs750293221 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117976712 | GTACAATTGCATAAA[A/G]CAGGAGAGAAAGACA | 90293 |
rs750302121 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956001 | CTGGTTTTTCACCTA[A/G]AATGTTTTAGGGTCC | 90293 |
rs750307875 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093293 | AAATAATAACTAACA[C/T]TTATTAAATCTTATC | 90293 |
rs750313039 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944139 | AGACCCTGTTTGCCC[A/G]GGTATCACCAGTGGG | 90293 |
rs750333542 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117946525 | AGATCTTGTGTTTCT[C/T]CATAGGTATACATTG | 90293 |
rs750345670 | in-del | -/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118057023 | CCTGTTCCTTGGGAC[-/T]TTTTTTTCAGCAAAG | 90293 |
rs750365999 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117945632 | TTGTACAATTTACAA[C/T]GAGATTATTTAGAAA | 90293 |
rs750366692 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036018 | AGAGAATAAAATACC[G/T]AGGAGTCCAACTTAC | 90293 |
rs750376753 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900814 | CAAATGATAATAACC[A/T]GACTAACAAAGTTAA | 90293 |
rs750382286 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117914649 | TTTGGTAAGAACAAA[A/G]GGATAATTGAATAAT | 90293 |
rs750390676 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985745 | CTATTTGTTGTATTA[A/T]CTTTATTTTTTATTA | 90293 |
rs750397810 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085647 | ATGCTTTTGAATACC[C/T]CTAGCTTAGCTCCCA | 90293 |
rs750398532 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118068442 | GAGTCACATAAAGAA[C/T]GGAAGGAAATACTAG | 90293 |
rs750454283 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947534 | AGTAAACTACAAGTA[A/G]CAACTTATTTACTTT | 90293 |
rs750457050 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118105077 | CACATATACCAACAC[A/G]CACCTGTGCACACAC | 90293 |
rs750459266 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117976749 | ATAAAAGCTCTTCGA[C/T]GCATTTTATGAACAT | 90293 |
rs750470073 | snp | G/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029064 | GGTACTCTCCACGTT[G/T]TCAGGCATCCACTGG | 90293 |
rs750489836 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048462 | ATACTCTAGGAGCTT[C/T]ACCTGTATCTTTTTT | 90293 |
rs750501479 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118078451 | GCAAGCACTAACTTG[-/T]TTTCTGTCCCTATAA | 90293 |
rs750508653 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948076 | ACCCCCATGATTCAT[A/C]ATGTCTGCAGACATT | 90293 |
rs750508706 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939103 | CTAGCCCCCCACCCC[C/G]TGAAAGGCCCTGGTG | 90293 |
rs750523616 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083020 | GTGATTCCTCCAGTT[C/T]TGTTCTTTTTGCTAA | 90293 |
rs750523915 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963218 | ATGTGGGGGGGAAAT[-/G]GGTAAAAACAACAGA | 90293 |
rs750535683 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039286 | CAAGCAGGCTCCTAC[A/C/T]GTCCCCAATTCTAGG | 90293 |
rs750537006 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939179 | CCCACTTATGAGTGA[A/G]AACATCTGGTGTTTG | 90293 |
rs750579399 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036524 | ATAAATGATGCTGGG[-/A]AAACTGGCTAGCCAT | 90293 |
rs750583560 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999114 | TCAAAAGGTTCAAAA[C/T]AAAAAAAAGATAAAA | 90293 |
rs750584807 | in-del | -/A | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117967753 | GTCTTTTTAAAAAAT[-/A]ACACAATAGGCTTTA | 90293 |
rs750586697 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027686 | ACTTTCATACATGCC[C/T]CACCTTTCACACTTA | 90293 |
rs750591545 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118071199 | CTTTGCTATTGTGAA[C/T]AATGCCGCAATAAAC | 90293 |
rs750613613 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117906964 | ACCTATATTTACCAT[C/T]AGAGGGGAAATTTTT | 90293 |
rs750618633 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118062947 | GAAACTGTAGCCAAG[A/G]AATTGGAAGCAAAGA | 90293 |
rs750623028 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930587 | TCTATCACTTCGACA[C/T]TAGCAAATAACCAAA | 90293 |
rs750631400 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117939783 | ACACACTTTTTGATG[A/G]GGTGGTTTGTTTTTT | 90293 |
rs750660770 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107331 | TAAACTTTCTTGTCT[C/G]CCAGAAAACTAGTGT | 90293 |
rs750666950 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049596 | GGTGATTCTTCACTA[A/C]AGTAAATCTAAAAAT | 90293 |
rs750675077 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103697 | ATAACACTGACTGTA[A/G]CTTATTACTTTAATG | 90293 |
rs750681662 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071319 | TAGTTCTAGATCCCT[C/G]AGGAATCGCCACACT | 90293 |
rs750687005 | snp | A/T | 2.28279e-05 | 0.00337838 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899088 | ACAACGATTATTCCA[A/T]GAATACCCCCCAACC | 90293 |
rs750690406 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118010400 | ATACACCATGGAATA[C/G]TATGCAGCCATAAAA | 90293 |
rs750694147 | snp | A/G | 2.28504e-05 | 0.00338004 | missense | KLHL13 | GRCh38.p7 | X:117909546 | CTTGGGGCATCCATG[A/G]GGGCTAACGATTTCC | 90293 |
rs750697465 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981389 | ACAGAATTCATCTTC[C/T]AGGTTGAATCTAGAT | 90293 |
rs750711594 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118052556 | GTAGAGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 90293 |
rs750718711 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906188 | TCTATTTTTAAAAAG[C/T]GCTTGTAGGGTAGGG | 90293 |
rs750719440 | in-del | -/GGTGT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951467 | ATATCTTCTTAATGA[-/GGTGT]TTGCCTGAAAGGAAT | 90293 |
rs750753525 | in-del | -/TCTG | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118082617 | TTTGATGTAATCCCA[-/TCTG]TCTATTTTTGCTTAT | 90293 |
rs750753867 | in-del | -/TA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063925 | AGAGACAAAAATTAT[-/TA]TAGTTATTTTAGCAA | 90293 |
rs750755409 | in-del | -/AAAAAAAA/AAAAAAAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991137 | TTTTCATTAAAAAGT[-/AAAAAAAA/AAAAAAAAA]AAAAAAAAAAAAGTC | 90293 |
rs750769611 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045372 | GAGCAAGACTCCATC[-/AA]AAAAAAAAAAAAAAA | 90293 |
rs750776843 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022426 | CTATACTGTTTACCA[G/T]AATGGCTGTATCATT | 90293 |
rs750777720 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117961716 | CTGGAATGCAAGCAA[C/T]CTCTAGAAGCTGAAA | 90293 |
rs750781443 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117952144 | CATCACGCTACCTGA[C/T]TTCAAACTGTACTAC | 90293 |
rs750783177 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117920848 | GTATTAAGTACACGA[A/T]AGTTCTTTCTACTAA | 90293 |
rs750787834 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118042160 | CCAGAGGATATAAAA[C/T]TGTAAACATATATGC | 90293 |
rs750790651 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970133 | CCCACACATGCTCAA[C/T]CACTATAACACATTT | 90293 |
rs750795218 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108094 | GTGGAACAGAAAACT[C/T]TGTTGAAATGAAGTG | 90293 |
rs750797454 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971501 | ACAAACTAGCCTATT[G/T]TTTTTTTTACTTCAT | 90293 |
rs750802429 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093934 | AGCTCCAGTCTACAG[C/T]TCCCAACGTGAGCGA | 90293 |
rs750821595 | snp | G/T | 2.28141e-05 | 0.00337736 | missense | KLHL13 | GRCh38.p7 | X:117899288 | CTCCCACTGTACACA[G/T]GCAATGCAGACCTCT | 90293 |
rs750824804 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056856 | AGTTTGTTGTGAGGA[-/T]TATATGAACAGCTGA | 90293 |
rs750837957 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982165 | TAGATATACACATAG[A/G]AAACACAAATTAGTG | 90293 |
rs750841167 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044243 | AGTGGACACAACAAA[A/C]TGGAAAGATATTTCA | 90293 |
rs750845950 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118053085 | TATTCATTATACATA[A/C]AATATTCTAAAAACA | 90293 |
rs750855597 | in-del | -/CT | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117972300 | TCTGATCAATGTTAA[-/CT]CTGTTTTTAATTCAT | 90293 |
rs750855640 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118083454 | GAACTTAGAGGACAT[C/T]ATGCTAAGTGAAATA | 90293 |
rs750876954 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117988523 | TTATATTGGAAGCAA[C/T]TGCTCATGCTCCTAT | 90293 |
rs750886864 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117921923 | TAAAACAAGATTATA[G/T]ATCATATTTTTCTTT | 90293 |
rs750896870 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921436 | AGGCTACTAAAGTAC[A/G]CCAAAAGGGAACAAT | 90293 |
rs750897113 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118020596 | TGGCGATTCCTCAGG[A/G]ATCTAGAACTAGAAA | 90293 |
rs750900011 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911560 | CTCTAGCCTCCCAGC[C/T]TCCAACAGGCTCTGG | 90293 |
rs750905109 | snp | G/T | 2.36139e-05 | 0.00343604 | missense | KLHL13 | GRCh38.p7 | X:117919703 | TGCACATTAAATCTT[G/T]TTCTTTCATTCCACC | 90293 |
rs750906796 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117964957 | ATTCCATGGTGTATA[C/T]GTGCCACATTTTCTT | 90293 |
rs750907985 | snp | C/G | 2.28977e-05 | 0.00338354 | intron-variant | KLHL13 | GRCh38.p7 | X:117920380 | AAAGCCCTACAACAA[C/G]AACATGAGTTGAGTC | 90293 |
rs750908162 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028531 | AGCCAATATTTACTA[C/T]GAAGATTAACACTGG | 90293 |
rs750930459 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118021074 | TGCAGTGCACCAGCA[C/T]GGCACATGTATACAT | 90293 |
rs750938811 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944116 | TAGAGGTGCTAGAGG[C/T]CCACTCCAGACCCTG | 90293 |
rs750941893 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118068229 | TTCTGTTGGATCCAG[C/T]CTTCAGAACAGTATC | 90293 |
rs750949819 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973404 | TAGCCTTAGGCTACC[A/G]CTAATAGAGATCAGT | 90293 |
rs750960589 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922658 | TGTGGTAGTGGTAAA[C/G]GTTAAGGTAAGAGAA | 90293 |
rs750976544 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936780 | TGATCAGCTCTATTC[C/G]CTGTGAGACCTTCTC | 90293 |
rs750996769 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112505 | AGAAAGGCATGGCAT[C/T]CATTTGACAAGCACC | 90293 |
rs750997725 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069220 | CTGAGCAGCTGCACA[C/T]CCCTTCAGGAGGTAT | 90293 |
rs751008815 | snp | A/G | 0.123679 | 0.215738 | intron-variant | KLHL13 | GRCh38.p7 | X:118036475 | TTTGACTAACCGGAG[A/G]AAAACAAGAAATGGG | 90293 |
rs751010007 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086518 | TATGGTATGTGAATT[A/G]TATCTCAATTTTTTT | 90293 |
rs751033387 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118063163 | TAAGCTGGATTTCAC[C/T]AATAGGTCAATTAAT | 90293 |
rs751033584 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902560 | CCTGAAGATGGTTGG[C/T]GGCATAATATGAAGA | 90293 |
rs751036770 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994427 | CCCACTAATTTTTTT[-/A]TTTTTTTAGAGATGG | 90293 |
rs751050321 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118077892 | AATTCAAAATGAGAT[A/G]GCATATATAAAAGTA | 90293 |
rs751059831 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118031768 | AGGAACAGCTCCGGT[C/T]TACAGCTCCCAGCGT | 90293 |
rs751063071 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118054781 | TTTATCATATTCCTC[A/T]ATATTACATTAAAAA | 90293 |
rs751065887 | snp | A/G | 2.28219e-05 | 0.00337794 | missense | KLHL13 | GRCh38.p7 | X:117909589 | TTTCATCATACATGC[A/G]CAATTCCTTACTGAC | 90293 |
rs751075095 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118112462 | TGGGGAATAGTGTAA[C/T]AGGACCTGGAATTTG | 90293 |
rs751077399 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004147 | TGAGAAGTGAAATCA[C/T]GAAAAGGGAGAAAAC | 90293 |
rs751091212 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925808 | AAAATTTTTTTTCAC[C/G]TGGAATATCCTTCCT | 90293 |
rs751093051 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118094765 | AAAAGAATTTTCAAC[A/C]CAGAATTTCATATCC | 90293 |
rs751096891 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117903394 | TTCTCATTTTTACCT[A/G]CTGCTTTGTTGGCTT | 90293 |
rs751097053 | snp | G/T | 0.000356983 | 0.0133553 | intron-variant | KLHL13 | GRCh38.p7 | X:117985196 | GCTTGCTATTTTAAT[G/T]AGTAAGTAACAGCAG | 90293 |
rs751097317 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036932 | TCAAAAAGTGGGCAA[A/T]GGACATGAACAGACA | 90293 |
rs751104882 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118002168 | TTTGCCTAAATCACC[A/G]GGTTAGATGCACGAA | 90293 |
rs751105253 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986680 | CTCTTGCATGAAATC[G/T]CTTCCAAACTCCACT | 90293 |
rs751120154 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117983305 | ACAATACAATGATGC[A/G]TGGCATTTTTAACAG | 90293 |
rs751132682 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069730 | AAATTAAAAAGTGTA[A/C]AAAGTAAAAAGTTAC | 90293 |
rs751143405 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117949759 | CATGTTATACAGAAA[C/T]CCAGGTGTGGTCAAA | 90293 |
rs751146327 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926547 | TGAGTGGAAACCTTA[A/C]AAGGCTGGGGTTTTA | 90293 |
rs751151998 | in-del | -/GGCAT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118059055 | AGGAAGGCACACTAA[-/GGCAT]GACATAGAAGAAAAT | 90293 |
rs751155388 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015613 | TTCTCCCCAAGAACA[C/G]ATATACTTTCTATGA | 90293 |
rs751157317 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023695 | TGCCTCAGCCTCCCA[A/G]ATAGCTGGAATTACA | 90293 |
rs751158354 | in-del | -/AATAAAACTCAAAA | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117987839 | TGAGTGAAAAAACTG[-/AATAAAACTCAAAA]ACCAGTTGCCTTTCC | 90293 |
rs751166732 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113362 | AATGACCTTCCCCAG[G/T]AAAGACTCTTCAGTG | 90293 |
rs751193898 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958978 | CAGGCTATCTGCAGG[A/G]CTGGATCAGCAATCA | 90293 |
rs751197779 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907212 | TTCTAGTTCCTAGAT[G/T]GGTATACCATAGGAG | 90293 |
rs751211309 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950193 | AGTCCCAGGCTGGGC[A/G]TGGTGGCTCACGCCT | 90293 |
rs751226458 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000304 | TTCAGGCTGCAACCT[C/T]CTCTCCTGCCCCAGC | 90293 |
rs751241856 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118049705 | AGCCTATTTCAGAAC[A/G]CTCATTTTAAGTACA | 90293 |
rs751245031 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118008342 | AGTACTTAACCTATC[A/G]GCGTAAATGTATGCA | 90293 |
rs751258852 | snp | A/T | 2.28274e-05 | 0.00337834 | missense | KLHL13 | GRCh38.p7 | X:117899053 | TTATCTGGATCATAT[A/T]TCTGCACTATCTCTA | 90293 |
rs751262663 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951482 | GGTGTTTGCCTGAAA[C/G]GAATCAAGAAAGATA | 90293 |
rs751267237 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117917326 | TCTAAAACTGAGAGG[C/T]AGGAGTAAACTCTAT | 90293 |
rs751269682 | in-del | -/ACAA | 0.0743594 | 0.177906 | intron-variant | KLHL13 | GRCh38.p7 | X:118097289 | ATACACCTATAACAG[-/ACAA]ACAGAGAACCAGATC | 90293 |
rs751279640 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076210 | TTTAGAAAGAGGAGC[A/T]TAAGAAGAGAATGTT | 90293 |
rs751292693 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094121 | TCCTTTAGTTCAAGG[A/C]AAAGAAGTTAAAAAC | 90293 |
rs751300285 | in-del | -/TGAGGAAT | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118041020 | TTGACAAACAAAAGC[-/TGAGGAAT]TGAGGAATTTCATCA | 90293 |
rs751302935 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118097796 | TACAACTATCTGATC[G/T]TTGACAAACTGGAGG | 90293 |
rs751320959 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118086858 | GAAATATGTAGATTG[A/G]AATTCTTCCAGTCTA | 90293 |
rs751323072 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950501 | AAAGAAAGTCTCTTG[C/T]ATTAGTGTCAAAAGT | 90293 |
rs751328151 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050623 | TTTACTTTTTCCTTA[G/T]TCACCTAATTAAGGA | 90293 |
rs751329286 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025740 | CCCAGAACTTAAAAC[A/T]AAATTAATTTTTAAA | 90293 |
rs751352940 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118000625 | CATTTTAAAAGGCAA[C/G]CCCTTATCCACAATT | 90293 |
rs751367686 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039081 | GCCTTGAAGGGAAGG[A/T]CCCAGTCCTAAGCAG | 90293 |
rs751368464 | in-del | -/TAAG | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117970581 | GAATTATGCTATACT[-/TAAG]TATCATTTTGTGTGT | 90293 |
rs751374079 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118068230 | TCTGTTGGATCCAGC[C/G]TTCAGAACAGTATCA | 90293 |
rs751388824 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092036 | GGCATAAGAATGATA[C/T]ATTAGACTTTGGACA | 90293 |
rs751397354 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015247 | AACCTTAGTTACATT[A/T]AAAAATGTATCAGAA | 90293 |
rs751401020 | snp | C/G | 0.00240098 | 0.0345648 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909494 | TCCGCCAACCACATA[C/G]AGAAAATTTCCAATG | 90293 |
rs751401845 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065038 | TTCTTTAGCCTATAA[C/T]ACCTTCAACTGCTGG | 90293 |
rs751402015 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073231 | AAAATAAGGAGGTTT[A/C]ATGGACTTACAGTTC | 90293 |
rs751407487 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941569 | TTTAGTCTTGGGAGG[A/G]TGTATGTGTCTAGGA | 90293 |
rs751419621 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117963517 | ATTGTGAATAGTGCC[A/G]CAATAAACATACGTG | 90293 |
rs751429519 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917089 | GTTTAACTAAAAAAA[C/T]AGAATGCATGAAAGA | 90293 |
rs751441295 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943978 | ATTTATCTACCTTTG[G/T]TCTTTAATGTTGGTG | 90293 |
rs751447667 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | KLHL13 | GRCh38.p7 | X:118098382 | ACAATGAGATACCAA[C/T]TCACACCAGTTAGAA | 90293 |
rs751448627 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994135 | TCTTTCCATCAACCA[C/T]GAATGCCAATATTAA | 90293 |
rs751450374 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118016370 | ACTAAATTCAGTTAG[A/C]CTACTTTACAGTCTT | 90293 |
rs751461101 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985474 | AAAAAACCTATGTAC[C/T]GCATACCTTCCCTTG | 90293 |
rs751465629 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117954183 | TGTCCTTAAAGAACT[G/T]CAAAATAATATTTGC | 90293 |
rs751470356 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942629 | GTTTAAAGTCTGTTT[C/T]ATCAGAAACTAGGAT | 90293 |
rs751474052 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118119304 | CCAGCTAGAGTATCC[A/G]CTGACTTAGTTATTG | 90293 |
rs751478895 | snp | C/T | | | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898526 | CTTTTTACTTGAAGC[C/T]TAGTGAGCACAGTTG | 90293 |
rs751486955 | in-del | -/A/AA | 0.0613773 | 0.164171 | intron-variant | KLHL13 | GRCh38.p7 | X:117983435 | AACCAATTCGCACTG[-/A/AA]AAAAAAAAAAAAAGG | 90293 |
rs751490019 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065892 | TAAAATTCTACAGTA[C/T]CACAATAAGTTCCTT | 90293 |
rs751491199 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085351 | CATAGAAACAGAAAG[C/T]AGAATCATAATTGCC | 90293 |
rs751503953 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118012443 | TTGTGGCACCTTCCT[A/G]TATCTTCAAAGAGCA | 90293 |
rs751505638 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118019305 | CTTTTGAGAAGTGTC[C/T]GTTCATATCCTTCGC | 90293 |
rs751519988 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107842 | AGGCAGGAGGATTGC[C/T]TGAGCTCAGGACCAG | 90293 |
rs751532796 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117993459 | AAGCCTTATAATGCA[A/G]TTACTATTAACATCC | 90293 |
rs751533271 | snp | A/G | 2.28553e-05 | 0.0033804 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909868 | TCCGAGGCTCTTCCA[A/G]GCGAAGCCAACGACA | 90293 |
rs751539577 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118092663 | AAATTTTCTTTCCTT[C/G]CCCCTCCTCTTGAGT | 90293 |
rs751551407 | in-del | -/ATA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117929035 | ATAAGTATTAAAAGG[-/ATA]ATAAGGAAATATGAA | 90293 |
rs751557462 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029508 | TACATTTTAGTAATG[A/C]CGATGTATAACACTG | 90293 |
rs751561021 | in-del | -/AAA | 0.00117371 | 0.0241966 | intron-variant | KLHL13 | GRCh38.p7 | X:118084156 | AAACTCTGTCTCTAC[-/AAA]AAAAAAAAAAAAAAT | 90293 |
rs751566172 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118110036 | GAAAATACACCAATT[-/A]GTGTATTGGTAAAGA | 90293 |
rs751569328 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118035173 | GAGGTACAAGGAGGA[A/G]CTGGTACCATTCCTT | 90293 |
rs751587778 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118110761 | ATAAGTGTCTAATCA[C/T]ATTAAATAAGTTCTT | 90293 |
rs751589007 | snp | G/T | 2.49981e-05 | 0.00353531 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909332 | ATTTCGCCCACCAAC[G/T]GCATACAGATATCCT | 90293 |
rs751597792 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008624 | ATTTATTACTGCCAT[-/G]AATTAGTTTTAGGTA | 90293 |
rs751609238 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025843 | GCAGCTTGTGCTAGT[C/T]CTGCTGTCACACTCA | 90293 |
rs751611177 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047539 | ATATAAAACCAATAT[C/T]AGGTTGGTGTGAAAG | 90293 |
rs751613763 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055834 | ATAAAACATTAGATG[C/T]TTGCCCCCTAAAATT | 90293 |
rs751622209 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913686 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG | 90293 |
rs751622662 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911575 | CTCCAACAGGCTCTG[A/G]TGTGTGATGTTCCCC | 90293 |
rs751627728 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118077064 | CACATCCACCTCTGT[C/G]TTTCCTCTTGGCTTG | 90293 |
rs751636487 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056969 | AGCTACAGCCTCCCA[C/G]AGTATTTATTCCCCT | 90293 |
rs751645803 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030044 | AATTAAGCAAGCAGG[A/G]GGAGGGATTCTTCAT | 90293 |
rs751673483 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118005903 | TAATGATTTTAGCAG[A/T]CTTTTCTAGGGAAAA | 90293 |
rs751682885 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103488 | AATACTGAAAAAGTG[C/T]AAAATGACATTTCAA | 90293 |
rs751691102 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117924126 | GTGAATTTTATTCTA[C/T]GTTATGTCTATCTTT | 90293 |
rs751702284 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080189 | GAAGAAAACCTATGA[A/G]TACTCTTTTCAACAT | 90293 |
rs751707469 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118046587 | AAATGCTTGAGGGGA[A/T]GGACACCCCATTCTC | 90293 |
rs751724296 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118047300 | AGAAGGCAAGCAGCA[C/T]CCAAATATCAGAAAT | 90293 |
rs751730056 | in-del | -/ACACACACACACA | 0.00211696 | 0.0324653 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975204 | ACACACACACACAGC[-/ACACACACACACA]CACACACATGTATGA | 90293 |
rs751730748 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118070659 | TTTTTTTGTCTGCTT[C/G]TTCTATCAGTTACTG | 90293 |
rs751735785 | in-del | -/CTC | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118022472 | CAGTGTGTAAGGGTT[-/CTC]TTCTCTACATCCTCT | 90293 |
rs751742675 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117975869 | CAAACAAGTGAAGAT[A/C]ATTTTATTGTAAAGA | 90293 |
rs751747312 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077797 | TGACAATCCCTACTT[C/T]ACAATTGTATTCATA | 90293 |
rs751749218 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928173 | TGTCTGTGTGTTTAA[C/T]AGCAGAGTTTCAAAA | 90293 |
rs751756745 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997755 | TCCTCATTTGTTCCC[C/G]TATTTTAGCACCCAG | 90293 |
rs751769618 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016624 | CTCTGAAAGGGCTCC[C/G]TTAGGCATAAGCAAA | 90293 |
rs751781673 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117939048 | TGCACCCATCAACCC[A/G]TCATCTACATTAGGT | 90293 |
rs751783731 | snp | C/T | 2.28595e-05 | 0.00338071 | missense | KLHL13 | GRCh38.p7 | X:117901928 | TCATTTGTTCTTGGA[C/T]TGTAACATTCTACTG | 90293 |
rs751786740 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117988885 | TTCAAGATTGACTAC[A/G]AAATATACCAACTTA | 90293 |
rs751787990 | snp | C/T | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118119045 | AATATGACTGGTGTC[C/T]TTTTAAGAAGAGTTT | 90293 |
rs751790577 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996184 | TGACATACAAGGAAA[A/G]AGGTTCATTCTCATC | 90293 |
rs751796955 | snp | A/C | 2.31203e-05 | 0.00339994 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972806 | CAGATAGCAGGAGAG[A/C]TCGTTTTCCATTTCA | 90293 |
rs751818353 | in-del | -/AAAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118072639 | AAATTTACAAGAAAA[-/AAAC]AAACAACCCCATCAA | 90293 |
rs751818561 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118061540 | AGGACAAAGTCTTTA[C/T]GGAGGCAGAAGCTTG | 90293 |
rs751823715 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118023024 | TTTCAGGCCTTACAC[C/T]TTGGTATGTAATCCA | 90293 |
rs751825269 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118038221 | GATTGGGAAATGTTA[C/T]TCAAGTGAAGGCAAT | 90293 |
rs751830710 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959931 | GGAGTGCAGTTAGGT[A/C]CAGAGGGATCGCATA | 90293 |
rs751833552 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118078402 | TCCAAATTTCCTTGA[G/T]GTGGAATCATCCACT | 90293 |
rs751841801 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046255 | ACATGGATGGAACTG[C/G]AGGACATTGTGTTAA | 90293 |
rs751844039 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905936 | TTTTTGTACCCATCA[A/C]ATTTTTCTTTTTATA | 90293 |
rs751844519 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927858 | ACCAAGGGGTAACAG[A/G]AGGGAGTATGCTGAG | 90293 |
rs751849737 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910480 | AAGGTTGTTCTATTA[G/T]GATTCATCTCAATCC | 90293 |
rs751855826 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008602 | TAAAAAGATCATCAT[A/G]AGAAGTATTTATTAC | 90293 |
rs751859645 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118009127 | GTAAATTTGTTTGAG[C/T]TCATTGTAGATTCTG | 90293 |
rs751880308 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951450 | ATTGTTGTTTAAAGA[A/C]TATATCTTCTTAATG | 90293 |
rs751882911 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111087 | TACCTCCCTAATCTC[C/T]ACCACCCACAGCAAC | 90293 |
rs751884053 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117977273 | TCCAAAATCTTAATT[-/C]CAGAAGATGTTTAAG | 90293 |
rs751899940 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118071054 | GAATGATGATTTCCA[A/G]CTTCATCCATGTCCC | 90293 |
rs751902874 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040416 | GCTGAAAAATACAAA[C/T]GACATACTGAAGAAT | 90293 |
rs751911533 | snp | C/T | 2.28809e-05 | 0.0033823 | missense | KLHL13 | GRCh38.p7 | X:117919661 | TAATTTTCCTTAGAC[C/T]GACTTTGCTCACACC | 90293 |
rs751912727 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118039229 | CCCAGAACATTCCTA[C/G]ATGTGTTAGCTATGT | 90293 |
rs751940784 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118017493 | AACCAATTGGTTATT[A/G]CAGGACGTCAGGCAA | 90293 |
rs751948359 | snp | A/G | 0.000541438 | 0.0164446 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898876 | ACACATTGCAAAGAT[A/G]GAACTACAGCATCTT | 90293 |
rs751964763 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117980580 | AAAATACTTATAGAG[G/T]AATCAAAATAACATT | 90293 |
rs751984095 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117960872 | GGAGTTATTCTGAAT[G/T]ATTCCGCTTGTTGCA | 90293 |
rs751986919 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903137 | GGTGACAGGCAAAAC[-/AC]ACACACACACACACA | 90293 |
rs752002313 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032661 | CAGAGCAGAAAAACT[A/G]GAAACTCTAAAAAGC | 90293 |
rs752004518 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118062985 | AAAGAAAAAAATAGA[C/G]AAGTGGTTTATAAGA | 90293 |
rs752008472 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968390 | AGGGGTTTGGACTTT[A/C]TAAATGACTTTTAAG | 90293 |
rs752017279 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118082427 | GAGAAACAGCTCTTC[C/T]GCTCTTTTGCCAATT | 90293 |
rs752024003 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081535 | GCATATAATGTGCAG[G/T]GTTCAAATCTGGGTA | 90293 |
rs752036097 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007327 | GGTGGGAGAATCACT[C/T]GAGCCACTGCACTCC | 90293 |
rs752038225 | snp | A/T | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:118010341 | ACTTGGAACCAACCC[A/T]AATGTCCAACAATGA | 90293 |
rs752043106 | snp | G/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:117919774 | ATGGTCAAACTCACT[G/T]CTGCTGCTAATTAGA | 90293 |
rs752043751 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099643 | ACACAGCAACACCTC[A/G]TCTCTAATAAAAATT | 90293 |
rs752058850 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957146 | ATCTCTCTCTAGAAT[A/G]CTCCTATCCTTCAAC | 90293 |
rs752069398 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938756 | ACTTTAGTATACCAA[A/C]AACACTTCTTCCTCA | 90293 |
rs752085454 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118026860 | CACATAGATCAGCTG[A/C]AGACAAGAAAAGAGC | 90293 |
rs752087589 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981246 | GTTGTAAAATAATCA[A/C]AGCTTGTTTTGGCAT | 90293 |
rs752088514 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032925 | CTGAAAACCAAGGCT[C/T]GAGAACTACGTGAAG | 90293 |
rs752099224 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093789 | TATTACAGGTTTTCA[G/T]GTTGTTATACAAGCA | 90293 |
rs752099508 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117952067 | ACTTTAAAGTTCATA[C/T]GGAACCAAAAAAGAG | 90293 |
rs752125141 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118002449 | AAATACAAAATTAGC[C/T]GGGCGTGGTGCTGCA | 90293 |
rs752147163 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043575 | CAGGGATGCAAGGAT[A/G]GTTCAACATACATAA | 90293 |
rs752152933 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117943393 | GCTAGGTTGGGGAAG[C/T]TCTCCTGGAGAATAC | 90293 |
rs752153839 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107978 | AGATCACTTGAACTT[A/G]GGAGGTTGAAGCTGT | 90293 |
rs752154267 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076115 | ATTTATAATTTATTT[C/T]ACAACAGTTTTTGTC | 90293 |
rs752164170 | in-del | -/CAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057955 | AGCTTCCTTTAGGCC[-/CAAA]CAGTCATCTTCCAGT | 90293 |
rs752166363 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118020507 | ACAGGTGCTGGAGAG[C/G]ATGTGGAGAAATAGG | 90293 |
rs752170032 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117910463 | GAAACTTGGGAAAAT[A/G]GAAGGTTGTTCTATT | 90293 |
rs752177108 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020109 | TTTTCACGATATTGA[A/T]TCTTCCTACCCATGA | 90293 |
rs752178503 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081461 | GATTTTTGGTTTTTT[C/T]TAACTGATACATAAT | 90293 |
rs752183172 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117964379 | TTTAACCTGTTTGTC[G/T]TGGTTCCAAATTTTC | 90293 |
rs752195163 | snp | A/T | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985885 | TGAGCTACTTCAAAA[A/T]TACATATAACTCATC | 90293 |
rs752201515 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074452 | TCTTCACTTATCATG[A/C]AAACTGCCAGGCCAG | 90293 |
rs752205339 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117964932 | TCATCATTTTTTATG[A/G]CTGCATAGTATTCCA | 90293 |
rs752230779 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117935844 | TTGAGAAAAGAGTTG[A/G]GGGCAACTGGGGAGT | 90293 |
rs752246259 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036905 | tttacaagaaaaaaa[A/C]aaacaaccccatcaa | 90293 |
rs752249677 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994713 | TTTAGGTTGGAAGTT[G/T]TTCCTAAGGCAAAAG | 90293 |
rs752250602 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118021953 | TGAGATGGTATCTCA[C/T]TGTGGTTTTGATTTG | 90293 |
rs752256166 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050308 | CTCATCATTGCAATT[A/G]GCTTTTTTGCCAATA | 90293 |
rs752266605 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903790 | TATCATCTTCATCTG[C/G]TTGAAGCCAAAGACA | 90293 |
rs752292216 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017996 | TCACCACAACGTGTC[C/T]TCCTAGACATTACCA | 90293 |
rs752322615 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922522 | AGCCATGTAGTCACA[A/T]TGGGTAGGATGTAAA | 90293 |
rs752324769 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112313 | AACAATGAGCAAACC[A/G]GATGAGGTCTAGGTC | 90293 |
rs752332385 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118094199 | GAAGTCCTTAAAGGA[C/T]CTGATGGAGCTGAAA | 90293 |
rs752338980 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936641 | ACTGTTCTGCTCTGT[C/T]TAGGTGAGACTTAAA | 90293 |
rs752340603 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041816 | GGAAAGGAGGAAGAG[A/G]AGACCATAAAACAAC | 90293 |
rs752342092 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118112284 | GCATACCATGTGCTG[A/G]GTGCTCAGAATACAA | 90293 |
rs752365550 | in-del | -/A | 0.00844089 | 0.0644143 | intron-variant | KLHL13 | GRCh38.p7 | X:118086462 | CTTTGTGAACATACT[-/A]AAAAAAAACACTGAT | 90293 |
rs752365648 | snp | A/G | 4.56241e-05 | 0.00477598 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117919611 | TTGAAGGTTGTCCAT[A/G]TTAAGAGAAAGCTTT | 90293 |
rs752396680 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006715 | GAGAAAGTATTTCTG[C/T]TCTAAAAACAAAAAA | 90293 |
rs752398872 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117947923 | ATGCTTAAAGGAATG[A/C]TTATCTGAGTAATTC | 90293 |
rs752432943 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092540 | CAGCATACCTACCCT[A/G]TTAGTTAAAAGAAGT | 90293 |
rs752438306 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032014 | GCATCACTCCCACCC[A/G]AATACTGCGCTTTTC | 90293 |
rs752451231 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031689 | AACTAAAATTTTTAG[A/C]CAGATCATATATATA | 90293 |
rs752459036 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118049583 | TGTTGCATTGAGTGG[C/T]GATTCTTCACTACAG | 90293 |
rs752460705 | snp | A/G | 4.56137e-05 | 0.00477543 | missense | KLHL13 | GRCh38.p7 | X:117909817 | GTGTCATCAGTGGAA[A/G]TCGTATGTTCTTCAT | 90293 |
rs752471738 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107393 | GATGCACATTCGAAA[A/G]ATAGCATTCCAGCTA | 90293 |
rs752471767 | snp | C/T | 4.56413e-05 | 0.00477688 | missense | KLHL13 | GRCh38.p7 | X:117909584 | GGCCTTTTCATCATA[C/T]ATGCGCAATTCCTTA | 90293 |
rs752473621 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048563 | ACTGTTATATTGTAC[C/T]TTTCTGCATGTTTGG | 90293 |
rs752481847 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117977993 | AAACTATCAGATACA[A/T]TTAAAATTTCTTACT | 90293 |
rs752487142 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948181 | AGGCAAAAAAGTCAA[A/G]TGCCAAAGGTGAGAA | 90293 |
rs752490877 | in-del | -/AGAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117988823 | GGAACAAGAAATGAT[-/AGAC]AGTATCTCATTAGTA | 90293 |
rs752491386 | snp | G/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118071833 | GGAAATAAAAGAGGA[G/T]ACAAACAAATGGAAG | 90293 |
rs752500785 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118084868 | CCCATTCTACAAAAA[C/T]AGAAAAATTAGCCAG | 90293 |
rs752513385 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030618 | GGTCTAACAGGAGGT[A/G]TTTAGCCATGGGGGC | 90293 |
rs752528135 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000215 | GGCCAAACAAATGCA[G/T]CCGGGAGGACTTGTC | 90293 |
rs752539002 | snp | A/C/G | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:117940058 | TAGGTTTTCTTCCAG[A/C/G]GTTTTTATGGTTTTA | 90293 |
rs752542369 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933653 | AGCAAATAGACAAAT[G/T]AGAGTACATCAAACT | 90293 |
rs752543485 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118079988 | GCCACACACCTACAA[C/T]CATCAGATCTTTGAC | 90293 |
rs752543931 | in-del | -/TATGT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994450 | GAGATGGGGTCTCGC[-/TATGT]TATGTTGCCCAGGCT | 90293 |
rs752551748 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968564 | TCCACATAATTTTGT[C/T]AAATTGTGCATAAGT | 90293 |
rs752555305 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013127 | AAGTTGAACAAGATG[C/T]CTGGCCTCTTGGAGC | 90293 |
rs752560783 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940587 | TGAGCACAGAATGTT[C/T]TTCCATTTGTTTGTG | 90293 |
rs752567467 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117916556 | AACTGGTATCTCTAT[C/T]CCACCAAAGGTGAGT | 90293 |
rs752579444 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991803 | TAGGCAAAGCTCTTG[C/G]CCAAAGCTTTCCTTA | 90293 |
rs752619749 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097255 | ACAAAATCAATGTGC[A/G]AAAATCACAAGCATT | 90293 |
rs752630229 | in-del | -/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118048684 | ATAGAAAGGCCAACA[-/T]TTTTTTTAAAGAGCT | 90293 |
rs752634130 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018265 | TTTCATAACAATTTT[C/T]TTCGTGATATATATT | 90293 |
rs752636808 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118105624 | AAATTGACTCATGTT[C/G]TCTGTTGCCCCTGGC | 90293 |
rs752642637 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117908462 | ACTCTATTTATAATA[C/G]AGAATAAAATAATTG | 90293 |
rs752659826 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914382 | AAGGGAAATGCAAAG[A/T]CTAAGAAATCTGGCA | 90293 |
rs752683997 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072787 | GATGAATTGAAGCCT[A/G]TATCATGATGTCAAA | 90293 |
rs752692288 | snp | A/C | 0.000318598 | 0.0126174 | missense, intron-variant | KLHL13 | GRCh38.p7 | X:117983514 | ATATATCCTTGAAAT[A/C]GGCTTGTTTTAATGA | 90293 |
rs752693755 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044705 | AAGAATGAAAGTAGA[A/C]CCCTATCTCTCACCA | 90293 |
rs752709670 | snp | C/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118097749 | TAGACCAATGGAACA[C/G]AACAGAGCCCTCAGA | 90293 |
rs752716028 | in-del | -/A | 0.000529942 | 0.0162693 | intron-variant | KLHL13 | GRCh38.p7 | X:118091279 | AACTTAAAGTATAAT[-/A]AAAAAAGTATCAATA | 90293 |
rs752722062 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018609 | TTTGGAAATAATGTA[A/T]CTCTTCTTAGCATTC | 90293 |
rs752722394 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118119155 | GGGCTTCAGAAGAAA[A/C]CAAACTTACCTACAC | 90293 |
rs752761005 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908333 | CGTGCCATGGTGGTT[C/T]GCTGCACCCATCAAC | 90293 |
rs752762593 | snp | A/G | 9.2523e-05 | 0.00680095 | missense | KLHL13 | GRCh38.p7 | X:117899348 | ATTTGTCAGTATCAG[A/G]GTCAAAGCACATGAG | 90293 |
rs752778441 | in-del | -/TTTG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041624 | GTTTTCTCTTGCTTA[-/TTTG]TTTGATTATTTACAC | 90293 |
rs752778569 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914865 | CCCAGGCTAGGCCTC[-/T]TCTTCCCAGACAGAG | 90293 |
rs752783662 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118084135 | GATCAGCCTGAGCAA[A/C]ATAATGAAACTCTGT | 90293 |
rs752789245 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115677 | AATGGAGCCAGGCAT[C/T]ACAATTCCCACCAAT | 90293 |
rs752796158 | in-del | -/T | 0.128718 | 0.218611 | intron-variant | KLHL13 | GRCh38.p7 | X:118012754 | ACTATAAAGTTACCA[-/T]TTTTTTTTTCCATTC | 90293 |
rs752809119 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922197 | CTCTTTTTTTGTTTT[A/G]TTTTTTTGAGACAGA | 90293 |
rs752812853 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012270 | CACTGTGACAAATGA[A/T]CACAAATGGTGGCTT | 90293 |
rs752814828 | snp | A/G | 2.63793e-05 | 0.00363166 | intron-variant | KLHL13 | GRCh38.p7 | X:117945599 | TTTTTTACATAAGAA[A/G]GAAGGGGAAATTAAA | 90293 |
rs752831359 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117954061 | ATATAACACTATGAC[A/G]TAGATAAGGGAATTG | 90293 |
rs752843708 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118034255 | CCTAATAGACATCTA[C/G]AGAACTCTCCACCCC | 90293 |
rs752847917 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922966 | AAGTGGGTTACTATA[C/T]ATACTGTTGTGCATT | 90293 |
rs752850699 | snp | C/T | 2.2843e-05 | 0.0033795 | missense | KLHL13 | GRCh38.p7 | X:117901891 | ATAGTGGGGCTCACT[C/T]ATTTTGGCAACATAG | 90293 |
rs752857507 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117954956 | GAGCTTTGCTTCCAG[A/G]GGACTTGTTAACCAA | 90293 |
rs752860798 | in-del | -/AATT | 0.00158814 | 0.0281345 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973506 | AAAGCCCGTTTCAAA[-/AATT]CCAGTCCCTCTGCTT | 90293 |
rs752866603 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101401 | ACTGAGTTAGCCCCT[A/G]TCCTCAAGGAATTCA | 90293 |
rs752873643 | snp | C/T | 2.28993e-05 | 0.00338365 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117945482 | AAAGATGCGTGTAGG[C/T]CCTGCCTTGGAAGAC | 90293 |
rs752889915 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943637 | TATTGATACTTTTGT[A/T]TGCTTCATGAAGTCC | 90293 |
rs752926034 | in-del | -/A | 0.297817 | 0.245384 | intron-variant | KLHL13 | GRCh38.p7 | X:117996831 | AATCATAGCCTATTT[-/A]AAAAAAAAAAAAAAG | 90293 |
rs752930803 | in-del | -/TG | 0.108827 | 0.206325 | intron-variant | KLHL13 | GRCh38.p7 | X:118021708 | AAACATACGTGTGCA[-/TG]TGTCTTTATAGCAGC | 90293 |
rs752934803 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965833 | AATAGATGCAGAAAA[A/G]GCCTTTGACAAAATT | 90293 |
rs752958213 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117945066 | ACCTTGTAATACTTA[C/T]TTTGATTGCTATGGA | 90293 |
rs752963297 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045542 | GACATGATGGTTCAC[A/G]CCTGTAATCCCAGCA | 90293 |
rs752967110 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055741 | TGGCCAACACAGCAA[C/G]ACCCTCAGCTCTAAG | 90293 |
rs752972861 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913575 | ACAAGGCCGGGGGCG[C/G]TGGCTCACGCCTGTA | 90293 |
rs752973639 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904859 | CTAGAGAATTAACTT[C/G]AGTAGTTTGGTGGCC | 90293 |
rs752983002 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118086590 | CTGATATAGAAATAT[G/T]TATAATATAAAGTTT | 90293 |
rs752983163 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066509 | TCAAAGTGGATCACA[A/G]ATCTAAATATAAAAC | 90293 |
rs752993663 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924337 | AAGTATGCATACATT[A/G]AAAGAAAAAGAGAGA | 90293 |
rs753008429 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059395 | CACTTTTCTTCTCAC[G/T]CTGTTTCCACTACAA | 90293 |
rs753012823 | snp | G/T | 0.0266548 | 0.112325 | intron-variant | KLHL13 | GRCh38.p7 | X:117966334 | agagaataaaatacc[G/T]aggaatccaacttac | 90293 |
rs753019756 | in-del | -/ACTG | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069875 | TCACATTCTCTTCTC[-/ACTG]ACTGACACCCATAAC | 90293 |
rs753042045 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007369 | AGAAGGAGACCCTGT[-/AA]CAAAAAAAAAAAAAA | 90293 |
rs753057079 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118046338 | TGGGAGCTAAAAATT[A/G]AAATGATTGAACTCA | 90293 |
rs753057685 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959139 | CAGCAACATTTCTAT[A/G]AAAAGTATATTAATG | 90293 |
rs753057915 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117937737 | TTTTTAATAGCTTTA[C/T]TGAGATACAATTTGA | 90293 |
rs753097673 | snp | C/G | 2.83917e-05 | 0.00376763 | intron-variant | KLHL13 | GRCh38.p7 | X:117910130 | AAAATTAAAACATGA[C/G]TACTTTCATGGCAAT | 90293 |
rs753101481 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118060183 | ATACTTATCTCAGCA[A/T]ATTCCCAGGGGACAG | 90293 |
rs753109734 | in-del | -/T | 0.00430568 | 0.0461985 | intron-variant | KLHL13 | GRCh38.p7 | X:118070641 | TATAACCATAATAGA[-/T]TTTTTTTTTGTCTGC | 90293 |
rs753122247 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117941992 | AAATTTCTCTCTAAA[-/C]ACTGCTTTAGCTGTG | 90293 |
rs753122397 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113448 | TATTTATCGGTTATT[A/G]AGCTGCTTCTAGGCT | 90293 |
rs753160256 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117966468 | AGAATCAATATCATG[A/G]AAATGGCCATACTGC | 90293 |
rs753169137 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117950732 | ATAAAATACATATTG[C/T]TCACACTCACAATTT | 90293 |
rs753190439 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118106024 | CTCCTGCCTCAGCCT[A/C]CCGAGTAGCTGGGAC | 90293 |
rs753190762 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085431 | AGTAAAAGGAGATAG[-/AT]ATATATATATATTTC | 90293 |
rs753191842 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927398 | GAACCTTTCTCCTTG[A/G]TCAGAGAAGCAGTGA | 90293 |
rs753199125 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117905502 | GCACGTGTGCTAGTG[C/T]GTGCACACACACACA | 90293 |
rs753203777 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955452 | ATGTATTCAAAGCCC[A/G]TAATAAATTTACCAA | 90293 |
rs753212631 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118114401 | AGAGCAAAATGCTTA[C/T]GGCTAACTCATCCAC | 90293 |
rs753218807 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008577 | CTCTACATTCACTTC[A/C]TGCACTCTCTAAAAA | 90293 |
rs753223037 | in-del | -/ACAG | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118051676 | ACACCATATCCAGGA[-/ACAG]ACAAACTCAAAATCA | 90293 |
rs753223292 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112004 | CCCCTTTTTTACATA[C/T]GAGATAACTGAGGTA | 90293 |
rs753227082 | in-del | -/TAC | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117980419 | AAATTAATGAAATAG[-/TAC]TACTACCTTGAAAAA | 90293 |
rs753227671 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118032341 | GACTTAAATGTCCCT[A/G]TCTGACAGCTTTGAA | 90293 |
rs753232570 | in-del | -/TATTAATATTTA | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117989409 | GTCACCTCTGTATTG[-/TATTAATATTTA]TATTAATATTCATTT | 90293 |
rs753236909 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100603 | CAACCCAGCCCACCT[A/G]TCAGTCAGATACAAC | 90293 |
rs753240164 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074043 | GACTCCCTTGTCCTA[-/T]TTTTTTCTGCTTTTT | 90293 |
rs753245197 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910308 | AGGCTGACTAAAAGA[A/C]AATGATCAAAGTCAG | 90293 |
rs753258234 | snp | A/G | 2.28133e-05 | 0.0033773 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117919617 | GTTGTCCATATTAAG[A/G]GAAAGCTTTGCAGTA | 90293 |
rs753262714 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117936478 | GTATACCCATAACTT[A/C]TTTTTTTATTATATA | 90293 |
rs753267382 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118026042 | TGGATAAAGGGGGAC[C/T]ACTGTATACATTCCA | 90293 |
rs753274720 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117979568 | AAGGGAAATTTATAA[A/G]CAGAGGAGTGAAAAT | 90293 |
rs753282512 | snp | A/T | 0.000164731 | 0.00907405 | intron-variant | KLHL13 | GRCh38.p7 | X:117910111 | CCTATTAAGCCAATT[A/T]AAAAAAATTAAAACA | 90293 |
rs753285057 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078584 | TCCAAATTTTTGTAT[G/T]TATCAGTACTTTGTT | 90293 |
rs753297666 | in-del | -/AAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089586 | GAAAGAAAAGAAAAG[-/AAA]AGAGAGAGAGAGAGA | 90293 |
rs753309373 | snp | A/G | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:117918953 | ATTATGGTACATACC[A/G]TTATCAAACAGTTAA | 90293 |
rs753312510 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118016801 | CTTGAGGAACAAGTA[A/G]GATTTTAATAGTCAT | 90293 |
rs753312704 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040293 | CCAGTCTTAGAGAGA[C/T]AGGGATATGTCACAT | 90293 |
rs753315053 | in-del | -/A/AA | 0.136102 | 0.222907 | intron-variant | KLHL13 | GRCh38.p7 | X:118042919 | AATGACATTGAAATG[-/A/AA]AAAAAAAAAAATACA | 90293 |
rs753318347 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117929041 | ATTAAAAGGATAATA[A/C]GGAAATATGAACAAC | 90293 |
rs753324674 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118102211 | GATAATATCTCCAGA[C/T]AAGTCAAAAATTGAT | 90293 |
rs753349234 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942560 | CCTCTTCTTGTTGCA[C/T]TGATCCCTTTACCAT | 90293 |
rs753351914 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971500 | TACAAACTAGCCTAT[A/T]TTTTTTTTTACTTCA | 90293 |
rs753363506 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118001691 | CAACATGATGAAACC[A/G]TGTCTCTACCAAAAA | 90293 |
rs753371246 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081490 | ATAATTGGACATATT[G/T]TTGGGGTGCACATAA | 90293 |
rs753378791 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117993721 | AGTATATGAAACTTG[A/G]TTACATTATCTGTTG | 90293 |
rs753380892 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107081 | CAGAAAAATGTGTGA[A/C]CCCTGTGATTATCAG | 90293 |
rs753384821 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117910429 | ACCCCCAAAATACTG[A/G]TAAAATTCCTGCCAG | 90293 |
rs753413356 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117919248 | AGGCTGGTCTTGAAC[C/T]CCCAACCTTAGACGA | 90293 |
rs753429306 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118092828 | AAATATACTACAGTT[A/G]CATAAGATGTAGTCA | 90293 |
rs753454663 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117945918 | TGCATATAGTTAAAA[C/T]TAATTTGGAACACCT | 90293 |
rs753459177 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074591 | GAATTTATGACCATG[A/G]CAAACATTTTCCACT | 90293 |
rs753469081 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099557 | GCTCACACCTATAAT[A/C]TCAGCACTTTGGGAG | 90293 |
rs753492591 | snp | A/G | 0.000177384 | 0.00941596 | intron-variant | KLHL13 | GRCh38.p7 | X:117985205 | TTTAATGAGTAAGTA[A/G]CAGCAGTAAATAAAG | 90293 |
rs753494424 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117901312 | TATGAATGGTGTTTA[C/T]CAGAATACAGAGCAT | 90293 |
rs753501914 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118043476 | TGATGAACATTGATG[A/C]AAAAATCCTCCACAA | 90293 |
rs753522554 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117964249 | GCACTTTAACATGTG[C/T]TATCTACCTCCAGTT | 90293 |
rs753529579 | snp | A/G | 0.111166 | 0.207907 | intron-variant | KLHL13 | GRCh38.p7 | X:118020439 | AATCAAAACCACAGT[A/G]AGATACCATCTCACA | 90293 |
rs753534335 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118066986 | ATAGTTTCTCATTGT[A/G]AGTACAGTCATGCAT | 90293 |
rs753540580 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968349 | CCATCTTCGAGAGGT[G/T]TCATGGAATGAGTTC | 90293 |
rs753543198 | in-del | -/AA | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118075196 | CCACATAAGGGAGAT[-/AA]AACATAAACCACAGC | 90293 |
rs753563857 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117920745 | TCCTTTTCGCGATAA[C/T]TTAATAGTCCTTTTA | 90293 |
rs753578382 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117935697 | ACTCACTCACTATCA[C/T]GAGAACAGCAAAAGG | 90293 |
rs753596428 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118111113 | GCAACAACATACTAT[C/G]TGCAAGGCCCTGATT | 90293 |
rs753604260 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | KLHL13 | GRCh38.p7 | X:118036161 | ATCGTGAAAATGGCC[A/G]TACTGCCCAAGGTAA | 90293 |
rs753611466 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085751 | CCATCCAATTGCTGC[A/G]AAAGACATTATTTCA | 90293 |
rs753612526 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911908 | TTTTTAAAATACCTA[-/AC]ACATAACTGTAACAT | 90293 |
rs753617833 | snp | G/T | 2.41876e-05 | 0.00347753 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972840 | GCATGTTGTCACCAC[G/T]GTACTACAATAACAG | 90293 |
rs753626406 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118057835 | CATTTCAAAAAAAAA[A/G]AAGTGAAAAATCCTA | 90293 |
rs753629557 | in-del | -/CAAAAAAAAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007370 | AGAAGGAGACCCTGT[-/CAAAAAAAAAA]AAAAAAAAAAAAAGA | 90293 |
rs753643397 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117964820 | TCAATTCCCACCTGT[G/T]AGTGAGAACATGCAG | 90293 |
rs753648479 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956157 | TCTACCAAAACTACC[A/G]TAAGTGTTTATCCAT | 90293 |
rs753650795 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118001344 | GGCCATGGATAGATG[A/G]TATTTAAGCAGCAAA | 90293 |
rs753656002 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006602 | CTTAACTCTGCCTTC[A/T]GCTCCTTTCAAAAAA | 90293 |
rs753659060 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006105 | TTTATCCATCTCCCT[A/G]CCACCCAGTGATTAT | 90293 |
rs753664518 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049990 | TTCATGTTGGCTATA[C/G]GTATACACCATACAC | 90293 |
rs753668248 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023183 | AATTATGCCTCTTTA[A/C]TGACATTGGACAGAA | 90293 |
rs753669991 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117976874 | GCCAACTCTTAGAAT[A/G]TAAAAGGAGAAGATT | 90293 |
rs753672089 | snp | G/T | 0.220835 | 0.248293 | intron-variant | KLHL13 | GRCh38.p7 | X:117983451 | AAAAAAAAAAAAAGG[G/T]GAGGAAAAATGTAGA | 90293 |
rs753687373 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118111753 | AAAAACTAGCCTGGC[A/G]TGGTGGCACGCACCT | 90293 |
rs753701966 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924999 | TTCAACCTCTATTAA[A/G]TAGAGAGAGGTACAT | 90293 |
rs753704156 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117980997 | TGACTATTTCCAGAT[C/G]CTTTTCGTTTTCCAA | 90293 |
rs753713157 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948154 | ACAGTTCTCTAGGTC[A/T]AAGCTGTTCTTAGGC | 90293 |
rs753713750 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051837 | AGAACTGAACACATA[A/C]AAATTGTCCAATAAG | 90293 |
rs753745604 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928699 | GATGAAGCTCTACTT[A/C]GGGGAAATTTATATC | 90293 |
rs753758405 | in-del | -/AC | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118017680 | AACAGCACTTAAGAA[-/AC]ACAATTATTTGTGTG | 90293 |
rs753772263 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118048500 | GATCTAAAACAAAAA[C/T]GGCAAAATTTTGAGG | 90293 |
rs753781130 | in-del | -/TATA | 0.122759 | 0.215197 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031545 | TATATATATATTAGT[-/TATA]TATATATTTAGTTAT | 90293 |
rs753781595 | snp | A/G | 2.56871e-05 | 0.0035837 | intron-variant | KLHL13 | GRCh38.p7 | X:117972695 | GTAGATTCATGAATG[A/G]AATCCCACTTTAATA | 90293 |
rs753790601 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977510 | ATTTTTTTCCTGATG[G/T]CCCCTAAGAAATTAT | 90293 |
rs753798537 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117967904 | AGGCAATTTGCAAAC[C/T]GTAAATTCACTAGGG | 90293 |
rs753809661 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118063634 | TAGCTTGTAAAGGAA[C/T]AGCCAAACTATTAAA | 90293 |
rs753836854 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999189 | CCAGCCATCCCATTA[C/T]TGGGTATATACCCAA | 90293 |
rs753854183 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096695 | TAAAATACTGGCAAA[A/C]CGAATCCAGCAACAC | 90293 |
rs753854216 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118023771 | GAGACAGGATTTCAC[C/T]ATGTTGGCCAGGCTG | 90293 |
rs753857931 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118049041 | AGTTTATGACCTAGC[A/G]TTTAATTAAAACCCA | 90293 |
rs753861175 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118012558 | ATGGGCCTGCCTGAA[C/T]GGTCCAGGATAATCT | 90293 |
rs753865125 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118042453 | ACAGGTCATATGTTG[A/G]GCCACAAAACAAGTA | 90293 |
rs753872259 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930599 | CACTAGCAAATAACC[-/A]AAAAATACTCAATTG | 90293 |
rs753890082 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074066 | TGCTTTTTTCCATTT[C/T]AGTTGCTCATTATAG | 90293 |
rs753904601 | snp | A/G | | | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899217 | TTCACAGCTTAGGAC[A/G]TCATCATAATCACTT | 90293 |
rs753915843 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071510 | CTCTGATGGCCAGTG[A/C]TGGTGAGCATTTTTT | 90293 |
rs753932626 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923009 | TGAGCAGATAACACA[A/G]ATAGTCTTCTATCTC | 90293 |
rs753939995 | in-del | -/TCTTAACTCTTTA | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118018214 | CTGACCTCCGCTCAC[-/TCTTAACTCTTTA]TATTTCCACCTACCT | 90293 |
rs753942399 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118091172 | TTAGGAGATATACCT[A/T]ATGTTAAATGACGAG | 90293 |
rs753945679 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117907864 | AAGAAAGGGTTTTAT[A/G]AACAGGAAAGTATAA | 90293 |
rs753952096 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118097183 | ATCTAGAAAACCCCA[C/T]TGTCTCAGCCCAAAA | 90293 |
rs753954505 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040766 | CAAGGCATTTAATTA[C/T]CAAACTCCCAAAGGT | 90293 |
rs753960206 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999839 | GAACGGAGAAATACT[A/G]TTTTTAAGCAAGAGC | 90293 |
rs753961558 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118108196 | ACTCTTATCTCCTTT[A/T]ACTGAATAGACTGTA | 90293 |
rs753969809 | in-del | -/TCTC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117958358 | TGAATGTGCTCTTTT[-/TCTC]TCTCTCTTTCTCAAA | 90293 |
rs753979757 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940540 | ACGTTGGGCAGTATG[G/T]CCATTTTCACGATAC | 90293 |
rs753983458 | snp | C/T | 2.28185e-05 | 0.00337768 | missense | KLHL13 | GRCh38.p7 | X:117899117 | CCACATAGATTTTAT[C/T]TTCGAAGACAGCGAC | 90293 |
rs753987513 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118033017 | TGAAATGAATGAAAT[A/G]AAGTGAGAAGGGAAG | 90293 |
rs753990379 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118011655 | TGAGAAAGGGTCCAG[G/T]ATGATGCCCGAGTTT | 90293 |
rs753993959 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117921126 | AGCTTTTTCACTACA[C/T]CCTGATGGTCTCAAC | 90293 |
rs754009596 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | KLHL13 | GRCh38.p7 | X:117945454 | ACACCACAGAACTGT[G/T]GGTATTGCTGGTAAA | 90293 |
rs754010572 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117961792 | TACAGCCACAAAGAA[C/T]GGAATTTTGTCAATG | 90293 |
rs754016149 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118395 | ACAATCACTTTTAGC[A/T]TGTATCAAAAACCTG | 90293 |
rs754021819 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118063974 | TTATATATTTTTTTC[C/T]GACTAAGTCTGAAGT | 90293 |
rs754028012 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942267 | GTGGTCAGTTTTACA[A/G]TAAGTGTAATGTGGT | 90293 |
rs754037074 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011116 | TAAGAAAAGGACACC[C/T]AATTCTGCTTGGAAG | 90293 |
rs754062958 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959509 | TTAAGATTTTGTAGA[G/T]CTGGTCTTTAATATT | 90293 |
rs754072452 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028672 | AATTGAATCTTATTT[A/T]AAAAACTGAAAGTAA | 90293 |
rs754088949 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100425 | CTTGCTACTTACACT[C/G]ACTTTCTCCATTAAG | 90293 |
rs754092305 | in-del | -/AGCTCTTTAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118019482 | CTTTTGCTGTGCAGA[-/AGCTCTTTAG]TTGAATTAGATCCCA | 90293 |
rs754107863 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064833 | TTCTAGGATAACAAC[A/G]CCTACTTCTCAAAGG | 90293 |
rs754117352 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045844 | AACTACACTGAGATA[C/T]CATCTCATCTCAGTT | 90293 |
rs754125507 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912671 | TTCTTTAAAATCACC[A/G]GAGAAAGGTATTCCA | 90293 |
rs754128807 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107332 | AAACTTTCTTGTCTG[C/T]CAGAAAACTAGTGTT | 90293 |
rs754130371 | in-del | -/TTTTTTTTTTTT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118105893 | TTTGGTCTAAACAGC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT | 90293 |
rs754137597 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118043807 | AATGGGAAAAAACTG[-/A]AAGCCTTTCTTCTAA | 90293 |
rs754152366 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117995572 | AGTGCATTCAGAATG[C/T]TGCGCAACCACCCCC | 90293 |
rs754166586 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936903 | GATTACAAATAAAAA[A/T]AGCTGGGCCAGAGAG | 90293 |
rs754175607 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076206 | CTTATTTAGAAAGAG[A/G]AGCATAAGAAGAGAA | 90293 |
rs754202214 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118004072 | TGTGTCAACAGGGCA[C/T]TGGCTACATGTGAAG | 90293 |
rs754223759 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951824 | CCTATTTAATCCTTG[C/T]AATAACTCATTTAAC | 90293 |
rs754241695 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029323 | AACACAATTTTAGAA[C/T]TGGTTGCAAAAAAAT | 90293 |
rs754253961 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:118045385 | TCAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA | 90293 |
rs754259690 | in-del | -/TT | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118076894 | TCTTCTCTTCTCCTC[-/TT]CTCTTCTTCTTCTCT | 90293 |
rs754277681 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004263 | GTATAAATGTGTATA[C/T]GTATTTATGTGTGTA | 90293 |
rs754279119 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906245 | AGGAACATTCAGAAA[G/T]ATAGGCAAGAGTTTC | 90293 |
rs754292926 | in-del | -/A | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974352 | CAACTACCTATTTTT[-/A]AAAAAATCACTGCAG | 90293 |
rs754304473 | snp | A/C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117972077 | CAGTGCACTTCAGTA[A/C/T]GTATTTACTTAAAAT | 90293 |
rs754306499 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117993359 | TGATGATAATGGCTA[A/G]CATTTGTTTGATCAC | 90293 |
rs754321122 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958015 | GATTGCTTCTAGTAA[A/C]ATTACTTTCAGTCTG | 90293 |
rs754324836 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117965691 | TCCAGCAGCACATCA[A/G]AAAGCTTATCCACCA | 90293 |
rs754338806 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094799 | CAAACTAAGCTTCAT[A/C]AGTGAAGGAGAAATA | 90293 |
rs754343824 | snp | A/C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114016 | AGATATTTTCTCTAG[A/C/G]GCTATTCATTTCTCT | 90293 |
rs754357048 | snp | A/G | 0.10742 | 0.205356 | intron-variant | KLHL13 | GRCh38.p7 | X:118021689 | ATTGTGAATAGTGTC[A/G]CAATAAACATACGTG | 90293 |
rs754357852 | snp | C/T | 0.000552334 | 0.0166091 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973427 | AGATCAGTGACTAAA[C/T]TCAGCAGCCTGCTTT | 90293 |
rs754383634 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117937758 | TACAATTTGAATACC[A/G]TACAATTTACCCATT | 90293 |
rs754401102 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907649 | AGGCCTAAAGAACAA[C/T]TGTACACTAAGGACA | 90293 |
rs754407716 | snp | C/T | 2.2877e-05 | 0.00338201 | missense | KLHL13 | GRCh38.p7 | X:117909870 | CGAGGCTCTTCCAGG[C/T]GAAGCCAACGACAGG | 90293 |
rs754409933 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117997396 | ATGAAAATAGAAAAT[A/G]CCTGAAAAGCAACAT | 90293 |
rs754413130 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093990 | TTCCAACTGAGGAAC[A/G]CAGCTCCTCACCAGC | 90293 |
rs754413679 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117946171 | TGTTATTAGTAGTAG[C/T]TCTAATCAACCCCAA | 90293 |
rs754419414 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926848 | AAACAGTCACCTGTC[A/G]ACAGACAGAAAAAGC | 90293 |
rs754425305 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942593 | TGAAATGCCCTTCTT[C/T]GTCTTTTTTTATCTT | 90293 |
rs754425830 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044258 | ATGGAAAGATATTTC[A/G]TCTTCATGGATTGGA | 90293 |
rs754434996 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938456 | TGTTAGAAATGCAAA[C/T]TCCTGGGCCTTATCC | 90293 |
rs754441159 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015748 | ATAAATTTCATGTGC[A/G]TCTACCATAAGATCT | 90293 |
rs754443814 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118098626 | AAGACACATGCACAC[A/G]TATGTTTATAGCGGC | 90293 |
rs754459526 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115393 | AAGCGATATCGCTAA[A/G]AGTGAGTAGTCTTTT | 90293 |
rs754479487 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928710 | ACTTAGGGGAAATTT[A/G]TATCAGTCAATGACT | 90293 |
rs754484674 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117971509 | GCCTATTTTTTTTTT[A/T]ACTTCATAAAGTTTA | 90293 |
rs754500838 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998839 | GAGCAAGCACACAGG[A/G]AACCATGAAGCAAAA | 90293 |
rs754502874 | in-del | -/AACAAGTTG | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118013109 | GCGATTAAAGCAGTA[-/AACAAGTTG]AACAAGATGCCTGGC | 90293 |
rs754504686 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092858 | ATTTGGGGAAACTGG[A/G]TGACAGGTACCCAGG | 90293 |
rs754510561 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117963825 | GATGGCCAGTGATGA[C/T]GAGCATTACATATAC | 90293 |
rs754515906 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118043487 | GATGCAAAAATCCTC[A/C]ACAAAATATTAGCAA | 90293 |
rs754520098 | snp | A/C | 2.39266e-05 | 0.00345872 | missense | KLHL13 | GRCh38.p7 | X:117910024 | AGACGAAACTGTTAA[A/C]GTATTTATCCACTTC | 90293 |
rs754525950 | in-del | -/A | 0.0058139 | 0.0536018 | intron-variant | KLHL13 | GRCh38.p7 | X:118067273 | TACAGTATAAAAGAT[-/A]AAAAATGGTACACCT | 90293 |
rs754528467 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117994504 | CAATCCTCCATCCTC[A/G]GTTTCCCAAAGTGCT | 90293 |
rs754532362 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118110916 | ACAGACGAGTCTTGG[C/T]TCATTTCAATTACAT | 90293 |
rs754533910 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020088 | TTACCTTGGGCAGTA[C/T]GGTCATTTTCACGAT | 90293 |
rs754543852 | in-del | -/T | 0.119531 | 0.213255 | intron-variant | KLHL13 | GRCh38.p7 | X:117993738 | TACATTATCTGTTGC[-/T]TTTTTTTTTTTTTTT | 90293 |
rs754590035 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073032 | CCTGGAGGTCAAGGC[C/T]TCAGCGAACCAAGAC | 90293 |
rs754591219 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118093445 | CAAATGACAGAATCA[C/G]ATTTTAGGTCAGGTT | 90293 |
rs754593813 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903725 | GGAAGCTTTTAGAAG[A/T]AATTAAACCACACAT | 90293 |
rs754597226 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117935794 | TGACACGAGATTTAG[A/G]TAGGGACACAGAGCC | 90293 |
rs754597300 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085241 | CTATAACTAAGACGA[A/T]CATTGAAAACGTTAT | 90293 |
rs754600082 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118036165 | TGAAAATGGCCATAC[C/T]GCCCAAGGTAATTTA | 90293 |
rs754600942 | in-del | -/ACATAGTAGCGC | 0.000529661 | 0.016265 | utr-variant-5-prime, intron-variant | KLHL13 | GRCh38.p7 | X:117985365 | CAGCTAGGCTCTGCT[-/ACATAGTAGCGC]ACCCCAGTGCATCTG | 90293 |
rs754611216 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901612 | TGGGTTCAAGAGATT[A/C]TCCTGCCTCAGCCTC | 90293 |
rs754623968 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118013741 | ACCCCCATGTTGCAG[C/G]AAGTCAGAGACCCCG | 90293 |
rs754650755 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985815 | CATTAAGTCCTATCT[G/T]TTTTTCTTTATCAAT | 90293 |
rs754675686 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118006111 | CATCTCCCTACCACC[C/T]AGTGATTATTAGATC | 90293 |
rs754688447 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030299 | CCTTCGATTTACCTT[C/T]TCTAAAACATGTTAA | 90293 |
rs754688822 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118067944 | TATCAAGTATTATGT[A/T]CTATATATATAACAG | 90293 |
rs754689301 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975417 | CTTTTTTGAGATGGA[G/T]TCTCCCTCTGTCACC | 90293 |
rs754713846 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014158 | GGGTTGGGCAGAACA[C/G]AGCCATATTTTTCTT | 90293 |
rs754714451 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947665 | AGCTGAAGAAGCCTG[A/G]ACTAAAATTATCTTT | 90293 |
rs754715540 | snp | A/T | 2.76182e-05 | 0.00371596 | intron-variant | KLHL13 | GRCh38.p7 | X:117910119 | GCCAATTAAAAAAAA[A/T]TAAAACATGACTACT | 90293 |
rs754730481 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117998712 | ACCTTCTGGAAAGTG[C/T]CCTACCAGAAATACT | 90293 |
rs754735116 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968361 | GGTGTCATGGAATGA[G/T]TTCCTGTGTTAAAAG | 90293 |
rs754735149 | in-del | -/CAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089633 | AGAGAAAGAAAGAAA[-/CAAA]GAAAGAAAGAAAGAA | 90293 |
rs754738245 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047703 | TTCACACACATGTGC[A/G]TGCACATGCACAACA | 90293 |
rs754742622 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117976978 | AGAGAAGCTAACTTG[C/T]CCAATGTTGTATCAC | 90293 |
rs754769406 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939265 | TCCCTGCAAAGGACA[A/T]GAACTCATCCTTTTA | 90293 |
rs754771953 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117914882 | CTTCCCAGACAGAGT[A/C]CCAGATAGCAGATAG | 90293 |
rs754772683 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118057858 | AAATCCTACAGAATA[A/G]GAGAAAATATTTGCA | 90293 |
rs754796695 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957516 | TTGCTTTTACATATT[C/G]ACAGCTATGCATTTT | 90293 |
rs754807866 | snp | A/G | 2.37304e-05 | 0.00344451 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909374 | TAGGTGGAAGAAGGT[A/G]CGCTTTTCATTTAAA | 90293 |
rs754824820 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079318 | AACAGAATGAAAAAA[A/C]GGTAACCAAATAGGA | 90293 |
rs754825408 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117915897 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGTG | 90293 |
rs754826118 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048543 | ACATGGTGGCTACAT[C/G]GGCAACTGTTATATT | 90293 |
rs754828386 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118039425 | GCACTTGAGCCTTGA[A/G]TGAACATCACTGGTA | 90293 |
rs754830360 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081987 | GTGTGTATACATATA[A/T]CAGCTTTTCTTTATC | 90293 |
rs754835967 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006603 | TTAACTCTGCCTTCA[A/G]CTCCTTTCAAAAAAA | 90293 |
rs754842034 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117948161 | TCTAGGTCAAAGCTG[C/T]TCTTAGGCAAAAAAG | 90293 |
rs754849856 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118103649 | GTCATTTTTTAATAA[G/T]AGAAAGGAAATAGTA | 90293 |
rs754867966 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023189 | GCCTCTTTACTGACA[C/T]TGGACAGAATTTACA | 90293 |
rs754874478 | in-del | -/TAAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104048 | AGGCCTCATTTCCAC[-/TAAAA]AAAAAAAAAAAAAAA | 90293 |
rs754889052 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117931015 | CAACATGACATTATC[A/C]GCAACCCAAGCATTT | 90293 |
rs754895334 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118071225 | TAAACATACGTGTGC[A/C]TGTGTCTTTATAGCG | 90293 |
rs754912770 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118071615 | CTCCTTAAGCTGATA[A/G]GCAACTTCAGCAAAG | 90293 |
rs754920141 | snp | G/T | 2.42607e-05 | 0.00348278 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972842 | ATGTTGTCACCACGG[G/T]ACTACAATAACAGTA | 90293 |
rs754925572 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968472 | TGCAAGCTCAGACAA[C/T]GCAAATTCCCAAAGA | 90293 |
rs754929655 | snp | A/G | 4.01373e-05 | 0.00447962 | intron-variant | KLHL13 | GRCh38.p7 | X:117901952 | TCTACTGTGGCTGTT[A/G]AAAAAAAAAAGAAAA | 90293 |
rs754934529 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074249 | TAAAACCCTCAACCA[C/T]AAATCTGTCAGCCCT | 90293 |
rs754934652 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048231 | TCATAATAGGAGATA[C/T]TAGAGCAGGTAAATC | 90293 |
rs754935453 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104378 | ATCAGTGTATACACA[C/T]AAAATTTCTCAGAAA | 90293 |
rs754939129 | snp | A/G | 2.51658e-05 | 0.00354715 | intron-variant | KLHL13 | GRCh38.p7 | X:117972707 | ATGAAATCCCACTTT[A/G]ATATCCTATTTTCTC | 90293 |
rs754942632 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118096749 | TCAAGTGGGCTTCAT[A/C]CCTGGGATGCAAGGC | 90293 |
rs754950641 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066089 | GGAGGTGGTGAAGAT[C/T]GTGAGTTCCAATTCA | 90293 |
rs754961198 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023796 | AGGCTGGTCTTGGAC[A/G]CTTAACCTCAGATAA | 90293 |
rs754990854 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118010820 | GCTCACGCCTGTAAT[C/T]CCAGTACTTTGGGAG | 90293 |
rs755002164 | in-del | -/A | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:117991138 | TTTTCATTAAAAAGT[-/A]AAAAAAAAAAAGTCT | 90293 |
rs755002908 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040835 | GAAACAAATAACATA[A/C]AATGGAGCTCCAATA | 90293 |
rs755004950 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991153 | AAAAAAAAAAAAGTC[C/T]TATAAATGAGAGTTG | 90293 |
rs755011705 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117961801 | AAAGAACGGAATTTT[C/G]TCAATGACAGGAATG | 90293 |
rs755027951 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118082862 | AAGAGACTTTCCTTT[C/T]CCTCACTGAATGTTC | 90293 |
rs755028827 | snp | A/C | 0.0797195 | 0.183042 | intron-variant | KLHL13 | GRCh38.p7 | X:118097215 | CTCCTTAAGCTGATA[A/C]GCAACTTCAGCAAAG | 90293 |
rs755040540 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118011658 | GAAAGGGTCCAGGAT[A/G]ATGCCCGAGTTTCTG | 90293 |
rs755052306 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069409 | TTTTTAACAAAAAAA[-/A]GTTTAAAATGTAAAA | 90293 |
rs755064676 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953353 | GATGGGAATTGAACA[A/G]TGAGAAAACATGGAC | 90293 |
rs755087255 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117972500 | ATGCCTTTGTACTTT[-/C]ACACTGGTAATTAGA | 90293 |
rs755119807 | in-del | -/AAAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011074 | TGAGACACTGTCTCA[-/AAAT]AAATAAATAAATAAA | 90293 |
rs755130901 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981650 | ATTTTTATGAATCTT[A/C]CACTACAGGGTCTAG | 90293 |
rs755151056 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924271 | ACACATTGTTGTGTA[C/G]AAGAAGGCAGTCATT | 90293 |
rs755151154 | snp | C/G | 2.28204e-05 | 0.00337782 | missense | KLHL13 | GRCh38.p7 | X:117899120 | CATAGATTTTATTTT[C/G]GAAGACAGCGACCCC | 90293 |
rs755156471 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075505 | AAAAAGAGAGAGGAA[A/G]GATTAATTGAAAGCT | 90293 |
rs755176755 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108963 | AGGCGTGTGCCTCCA[C/T]GCCCAGCTAATTTTT | 90293 |
rs755180016 | in-del | -/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117982550 | AGAGAAAAGTGGTTC[-/T]TTTCTCTATGCTGCA | 90293 |
rs755190833 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083566 | TAGAATAGTGGTTAT[C/T]AGAGGCTGGGCGAGA | 90293 |
rs755192234 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118053282 | TAAGAAAATGTGGCA[C/T]ATATACACCACGGAA | 90293 |
rs755192287 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117941083 | TTGGCTGTGGGTTTG[A/T]CATAAATAACACTTA | 90293 |
rs755212898 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028707 | ATCTATGAAATTTAA[C/T]AGTGAATCACTAAAT | 90293 |
rs755237960 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117988702 | AGGAAAAATGGCAAA[A/G]AAGGCAGAAGGCCAA | 90293 |
rs755238330 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117995637 | AAAATAAAACCCATA[C/T]CCATTAAGCAGTTGC | 90293 |
rs755254619 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004104 | AACTGGTCAAATAAT[-/A]AGAGACATGTTTCTT | 90293 |
rs755262016 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044723 | CTATCTCTCACCATA[C/T]AGAAACATCAAATCA | 90293 |
rs755275411 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933990 | TCCTCTGCAGCAACA[A/T]GGATACTGCTGGGGG | 90293 |
rs755282197 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118054008 | GAAAAAGACAATGAA[A/G]GAGAAAGAAGAAAAA | 90293 |
rs755282570 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973483 | AAATCAAGAATGCCA[A/T]TATGGGAAAAGCCCG | 90293 |
rs755283957 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117944358 | ACCCCAGCTCCAATT[A/G]GAAACGGAAATACTG | 90293 |
rs755303015 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094363 | TACAAAGAAATGAAC[A/C]AAGCCTTCAAGAAAT | 90293 |
rs755318459 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021701 | GTCGCAATAAACATA[C/T]GTGTGCATGTCTTTA | 90293 |
rs755320312 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094813 | TAAGTGAAGGAGAAA[C/T]AAAATACTTTACAGA | 90293 |
rs755332373 | in-del | -/TCTC | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118076906 | CTCTTCTCTTCTTCT[-/TCTC]TCTCTCTCTCTCCCT | 90293 |
rs755333950 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118069348 | AGTGAAATTGATTAT[C/T]CTAACCCTGTGTAGG | 90293 |
rs755337834 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951912 | TAAAAGAGGATACAA[A/G]CAAATGGAAGAACAT | 90293 |
rs755342769 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118112792 | AAGCTGGATTGCTTT[-/C]AAGGAAGGGCTTAGG | 90293 |
rs755350276 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036588 | ACCTTATACAAAAAT[A/C]AATTCAAAATGGATT | 90293 |
rs755357583 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004301 | GTATACAAATATTTC[A/C]TAGCTCTCTCCATCA | 90293 |
rs755379620 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117988062 | AAAATAAGCCAGACC[A/T]TTTCCTCATTTAGTT | 90293 |
rs755384988 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117903692 | GATTGGTACTTGGCA[C/T]TAGCAAAGCCATTAA | 90293 |
rs755399069 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987049 | GAATTGTGAAGAGAG[A/G]TGGACCTGTGTTGGG | 90293 |
rs755406222 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007850 | AAATTGCCATAGCTA[A/T]TAATAAGTCCCAAAG | 90293 |
rs755410479 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926950 | TCGCTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG | 90293 |
rs755420075 | in-del | -/A | 0.000534045 | 0.0163321 | intron-variant | KLHL13 | GRCh38.p7 | X:118069775 | AATTTATTACCAAAG[-/A]AAAAATATTTTTTAT | 90293 |
rs755434150 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117958059 | GTATTTCTCAGCAAC[A/G]ATGAACAGAATCTGG | 90293 |
rs755434954 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044391 | ATAATCCAAAAATTA[A/G]TAAGAACCACAAAAG | 90293 |
rs755436863 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904775 | ATTACTTGTGACAGA[C/G]ATTTAATGGCCCACA | 90293 |
rs755457835 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967949 | TATAATTAAAAAAAA[-/T]AATATAATCTCAGGC | 90293 |
rs755481366 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117949916 | ATGTCTAGCTCACAT[A/C]AAATAAAAAGCAACA | 90293 |
rs755483246 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959088 | TACTGCACATCATTT[A/T]AAAAAAACACTCTAA | 90293 |
rs755488349 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115576 | GCTTAGTTACCAGCC[C/T]ATGCTAACTTGAGCG | 90293 |
rs755493403 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032078 | ATATCCAGCACCTGG[C/T]TCAGAGGGTCCTAGG | 90293 |
rs755496269 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950483 | AAAAAAGGAAAAGAA[A/G]AAAAAGAAAGTCTCT | 90293 |
rs755500757 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113441 | CAAGTCCTATTTATC[A/G]GTTATTGAGCTGCTT | 90293 |
rs755501337 | snp | C/T | 0.187793 | 0.242137 | intron-variant | KLHL13 | GRCh38.p7 | X:117978793 | CTCTTTATGGCTTTT[C/T]TTTTTTTTTTTTTTT | 90293 |
rs755501603 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118097974 | CTAAAACCATAAAAA[A/C]CCTAGAAGGAAACCT | 90293 |
rs755507929 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015811 | AGAATTTTTAAACCA[A/C]AATAATTCCAATGTA | 90293 |
rs755511163 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015628 | GATATACTTTCTATG[A/C]CCTGGAAAATTCCTT | 90293 |
rs755518577 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073510 | AGCCAAACCATATCA[-/T]TCCCCCAATATCATC | 90293 |
rs755530362 | snp | A/C | 2.29316e-05 | 0.00338604 | missense | KLHL13 | GRCh38.p7 | X:117899321 | CAGTGGTCATTGGCG[A/C]CTTCTGGATCCATTT | 90293 |
rs755530848 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060117 | AACAGAGCATATAAA[C/T]GCTATGAATGAAGGT | 90293 |
rs755533518 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117917517 | ATGTTTCAACACAGG[C/T]TAAGGAACCAACAGT | 90293 |
rs755536366 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022555 | CAAGGTGATATCTCA[C/T]CGTGGTTTTCATTTA | 90293 |
rs755552949 | in-del | -/GGAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954408 | GGTAGATAGGTAGAC[-/GGAT]GGATGGATGGATGGA | 90293 |
rs755563429 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008555 | GAAGAGACAGGAGGA[C/T]ACATTCCTCTACATT | 90293 |
rs755583211 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118032311 | ACAAACAAAAAGACA[G/T]CAGTAACCTCTACAG | 90293 |
rs755590131 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023754 | TCTTTGTATTTTTAG[C/T]AGAGACAGGATTTCA | 90293 |
rs755602486 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118088715 | AACTTACGAAAAAGT[C/T]AGCAAGGCCAAAATA | 90293 |
rs755609589 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950654 | CTATGAATGGTTTAA[C/T]AACACAACAAAACAG | 90293 |
rs755639203 | snp | C/T | 0.00106355 | 0.0230357 | intron-variant | KLHL13 | GRCh38.p7 | X:118051648 | ACACTCACGCGCACA[C/T]ACACACACACACACA | 90293 |
rs755644588 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118097888 | CATATGTAGAAAGCT[A/G]AAACTGGATCCCTTC | 90293 |
rs755652748 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944267 | TACACAGCTTTAAGA[C/T]GCCAGGAGATGGAAA | 90293 |
rs755666958 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025929 | GTTTATATTTGTGAG[C/T]AGAAGAGATGAGCAG | 90293 |
rs755684593 | snp | C/T | | | missense | KLHL13 | GRCh38.p7 | X:117899024 | GCAGATCAAAAACCT[C/T]ATGCCATTCATCTTT | 90293 |
rs755685509 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118000902 | TGCTACCTTTCTAAA[A/C]TCCAAAAAGAATGTA | 90293 |
rs755689978 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117941740 | TTTTTCTTCATTAAT[A/C]TGGCTAGCGGTCTAT | 90293 |
rs755690835 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080891 | GTGGACTGGATAAAG[A/G]AAATGTGGTACACAG | 90293 |
rs755704665 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001560 | GAACACTGGACAAGA[C/T]GGAAGAAAAAGCCAC | 90293 |
rs755712987 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019378 | TTTGAGCTCATTGTA[C/G]ATTCTGGATATTAGC | 90293 |
rs755717479 | snp | C/T | 7.07255e-05 | 0.00594624 | missense | KLHL13 | GRCh38.p7 | X:117910012 | GAAAATTCTTCAAGA[C/T]GAAACTGTTAACGTA | 90293 |
rs755730052 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057340 | TACATTTGTGTATAC[C/G]ATATACAAATATTAA | 90293 |
rs755730861 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108027 | ACCACTGCACTCCAG[A/C]CTGAGTGACAGAATG | 90293 |
rs755738018 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901207 | AGCACGTTTTATGCA[C/T]AGGAGAACTTATATG | 90293 |
rs755743625 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117942485 | TTTGTAGATCTCTAC[A/G]AACTTGCTTAATGAA | 90293 |
rs755746753 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117898107 | CAGTATGTGCATACT[A/G]AATTCCCATTTTAAT | 90293 |
rs755749568 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109254 | ACCAAGGGTAACCAA[C/T]ATGTACCCTTGAAAT | 90293 |
rs755759814 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117993673 | GACTTCCAAGTTACT[A/G]AGAGAGAAAAAGGTA | 90293 |
rs755772461 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917630 | AAATTCTTTTCTATT[A/G]TTGTGACAGTAATAT | 90293 |
rs755783515 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038209 | GTGAAGTGATGAGAT[C/T]GGGAAATGTTACTCA | 90293 |
rs755786689 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117970900 | CAATGTCAAAATACT[C/T]CAGCCTACCATAAGC | 90293 |
rs755790792 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117962848 | AATTTGATGTGTAAC[A/T]TTAAGCAATTAACCT | 90293 |
rs755803006 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013057 | TTCAGCAAATATTTA[G/T]TGAGTAACTTGTCTG | 90293 |
rs755804992 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047934 | TATATGAAGAAAAGA[A/G]TAAGCAAGTGTGTCA | 90293 |
rs755822562 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117933029 | TTTGAGAAATGAAAT[A/G]TCTATTCAGGTCTTT | 90293 |
rs755829702 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118033578 | CCTGCCCTAAAACAG[A/C]TCCTGAAGGAAGCAC | 90293 |
rs755830570 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092746 | GTGGTTACATGAATC[C/T]ATAATGTGATAAAAT | 90293 |
rs755835891 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118042722 | GTAAACAAAACATAC[A/C]AAACCTATAAGATAC | 90293 |
rs755845414 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117963715 | CCTATTTCTCCACAT[C/G]CTCTCCAGCACCTGT | 90293 |
rs755861899 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955375 | AGACTCACAAAGTAG[C/T]AACCATTGCATTCCA | 90293 |
rs755898111 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118055981 | AATAATTTTTAAAAG[A/G]AAAAAAGGCACCCAT | 90293 |
rs755903145 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117912348 | AGACAAAATGATACT[A/T]CCAGTTGCCAGTCAC | 90293 |
rs755918419 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118110166 | AACCCAATTCATATC[A/G]TGGACGCTAAGAAGA | 90293 |
rs755923259 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910697 | GCAAATTAATTTTCA[A/G]CATTATTTATCTGGA | 90293 |
rs755924440 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117976733 | GAGAAAGACAACATA[C/T]ATAAAAGCTCTTCGA | 90293 |
rs755928395 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118035313 | ATTTTAGACCAATAT[C/T]CTTGATGAACATTGA | 90293 |
rs755928984 | snp | A/T | 2.58625e-05 | 0.00359591 | intron-variant | KLHL13 | GRCh38.p7 | X:117972685 | TTGCCACAAGGTAGA[A/T]TCATGAATGAAATCC | 90293 |
rs755944247 | in-del | -/TC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903618 | ATCCTACATTATTAT[-/TC]TCTCTCTCTCTCTCT | 90293 |
rs755968445 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102130 | GTCAAGTCATGATGG[A/G]CTTGTATACTCTGCT | 90293 |
rs755974219 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030178 | AAATGACATCATTTA[C/T]GTTTATTTGTACAAT | 90293 |
rs755978206 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117925861 | AGACCTCCTTTGTTG[C/T]TGTTGTTTTGTAGAG | 90293 |
rs755981492 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117956024 | TAGGGTCCACCATTT[C/T]ACTACACTCCTAGAA | 90293 |
rs755988310 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117945727 | TACGCTTGTACCACT[C/T]TTTATCTTAGAAGAA | 90293 |
rs755990638 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956035 | ATTTTACTACACTCC[C/T]AGAAAGCCAGTTTAA | 90293 |
rs756008278 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118110831 | TGTGCTAAAGAAGCA[C/T]AGGTTGGTTTAAATA | 90293 |
rs756011480 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975325 | CATAAAGCAGCTATA[C/T]ATTATGTAGTAAGGA | 90293 |
rs756037674 | in-del | -/ATT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118106961 | AATCCATAGGAAGAC[-/ATT]ATTCACAACAGAATT | 90293 |
rs756039968 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078011 | CAAGTTTTTGAGCAA[A/T]GCTCTTACTCTTTCT | 90293 |
rs756054929 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078540 | TCTGACCTCTTTTAG[C/T]TGATTAGCATTAACG | 90293 |
rs756073217 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118096248 | ATGACAAAGGGGGTA[C/T]CACCACCGATCCCAC | 90293 |
rs756076217 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047638 | AACCATAATAGAAAC[A/G]GGAAACAAATAAATG | 90293 |
rs756078982 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938735 | TTATTTTTCTTTAGC[A/G]AGAGCACTTTAGTAT | 90293 |
rs756091339 | in-del | -/AAAGAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089608 | GAGAGAGAGAGAGAG[-/AAAGAA]AGAGAAAGAAAGAGA | 90293 |
rs756093223 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089135 | TGCACCCTCATCCAC[A/G]TCACCAAAGGCTTAG | 90293 |
rs756094027 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083113 | TTGTTTTTATAAAAA[C/T]TATCATTGGTATTTT | 90293 |
rs756095189 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006074 | AGAACAGACTGGGTT[C/G]AGTTTCCATTCTATT | 90293 |
rs756108088 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117947535 | GTAAACTACAAGTAA[C/T]AACTTATTTACTTTG | 90293 |
rs756118252 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996693 | GTGTGATATACCAGG[C/T]TTTTTTTCCTAATCA | 90293 |
rs756134649 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117966991 | ATACCATTCAGGACA[C/T]AGGCATGGGCAAAGA | 90293 |
rs756147737 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987213 | AGAGCTGTAAGTGGA[C/G]AGAAATTGTGATTGT | 90293 |
rs756172596 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118070775 | TATTTATTATTATAC[-/T]TTTAAGTTTTAGGGT | 90293 |
rs756189600 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939280 | TGAACTCATCCTTTT[A/C]ATGGCTACATAGTAT | 90293 |
rs756198861 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089767 | ACCAAGAACCAGGAA[G/T]ATTCAGCTGCATTAA | 90293 |
rs756200613 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117988644 | ATGAATGGAAATGTC[A/T]TTTGCTGCTACTAAT | 90293 |
rs756204906 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118017668 | ATATGTCCTTTCAAC[A/G]GCACTTAAGAAACAC | 90293 |
rs756210685 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118032722 | GTTCCTCACCAGCAA[C/T]GGAACAAAGCTGGAC | 90293 |
rs756225102 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117980779 | AGAAACTACTGTCAT[C/T]TAAAAATAAAAGGTT | 90293 |
rs756243874 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117929576 | GAAAAAGAAAAATGC[C/T]AAGATCATTTCTTAA | 90293 |
rs756246955 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921465 | ATATGCAATTTAACA[A/G]TGATACAAAAAATGA | 90293 |
rs756257683 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117919882 | AAAGAAAGTACTTAA[A/G]AAAGATAATCTCTAT | 90293 |
rs756262616 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071201 | TTGCTATTGTGAATA[A/G]TGCCGCAATAAACAT | 90293 |
rs756280139 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117155 | GGACAACAGTGCAGC[C/T]GCCCCGGGTTAGCCA | 90293 |
rs756284695 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013603 | AAACTAAACCAATGT[-/G]ACAAACAAAATGTAC | 90293 |
rs756285950 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027738 | GCAATGTAGGTACTA[C/T]TATTAACACCATTTC | 90293 |
rs756286874 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081642 | ATATTCAATAAATTA[C/T]TGTTAACTACAGTCA | 90293 |
rs756288807 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118090230 | GGACATAGGCATGGG[C/T]GAGGACTTCATGTCT | 90293 |
rs756313084 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103858 | AGTCAGTGGCCGAAT[A/T]TTTTTTAATTCCAGT | 90293 |
rs756315359 | in-del | -/A | 2.42636e-05 | 0.00348299 | intron-variant | KLHL13 | GRCh38.p7 | X:117899406 | TCCTCCTAAAGAATG[-/A]AAACAATAGTTTTGA | 90293 |
rs756339710 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026873 | TGCAGACAAGAAAAG[-/A]GCTTTCAATGGAAAA | 90293 |
rs756350316 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118062973 | AAGAATAAGTAAAAG[-/A]AAAAAAATAGAGAAG | 90293 |
rs756352610 | snp | C/T | | | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898792 | TCTTTTTTCCAATAT[C/T]TGTATCAATTACCAG | 90293 |
rs756371834 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108112 | TTGAAATGAAGTGAT[C/G]TTTAGAAATGTATCA | 90293 |
rs756382292 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117910640 | TTCCTTCAAAGTTAT[C/T]ACTCATAATGAAAAT | 90293 |
rs756386846 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971714 | TTTCAAAGAAAGAGA[C/T]AGATATAATTGTGCA | 90293 |
rs756392095 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081785 | CATCATTCTTCTCTC[C/T]ACCTCCATGAAGTCA | 90293 |
rs756400864 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118053100 | AAATATTCTAAAAAC[A/G]TAACAGAAATACCAT | 90293 |
rs756408194 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029083 | GGCATCCACTGGGGG[C/T]CTTGGAACATACCAC | 90293 |
rs756413842 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117952166 | CTGTACTACAAGACT[A/T]CAGTAATCAAAACAG | 90293 |
rs756414824 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948706 | CTTGCATGCCACCCC[A/C]CGCCTACCCAATCAC | 90293 |
rs756418495 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117981573 | CCCTTTAGCTAGCAT[A/G]CATTTATTCATTCAT | 90293 |
rs756422055 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027062 | CACAAGCAAAAGTCA[A/C]AACAACAGTTATTTT | 90293 |
rs756441702 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118075388 | GCATTAGCAGTATTT[C/T]TCAAAATGCAGTTGA | 90293 |
rs756448106 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117972406 | AAGAAGTCATCCTAA[C/G]TGTTTTAGATATTCA | 90293 |
rs756451032 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117920930 | CTGGCCAAATATCTT[C/T]CAAGTTTCAAGTTTG | 90293 |
rs756463015 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957329 | TGAGTCACTGCTTGC[C/T]GAACAGAAGCCAAAT | 90293 |
rs756464596 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906226 | TAAAACCTCAGTTTC[G/T]GGCAGGAACATTCAG | 90293 |
rs756465662 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043651 | CCTTATGATCATTTC[A/G]ATTGATAATGAAAAA | 90293 |
rs756490248 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117943521 | TTGGAGGCTTTGTTC[A/G]TTTCTTTTCATTCTT | 90293 |
rs756508542 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911711 | AGCTTCATTCATGTC[C/T]CTACAAAGGATATGA | 90293 |
rs756511854 | in-del | -/ACAC | 0.167635 | 0.236043 | intron-variant | KLHL13 | GRCh38.p7 | X:118027649 | TCTCTCTCCACACAT[-/ACAC]ACACACACACACACA | 90293 |
rs756516893 | snp | A/G | 0.000162245 | 0.00900535 | intron-variant | KLHL13 | GRCh38.p7 | X:118028378 | CTATGTTAGGTATAT[A/G]AATAGGAAAGACGTT | 90293 |
rs756519059 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112514 | TGGCATCCATTTGAC[A/G]AGCACCCACTGTGCA | 90293 |
rs756521023 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922933 | ATGCTTGTATTAAAA[C/T]ATATAAAGGCCTCTT | 90293 |
rs756523350 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117995538 | CTGCACCTATCAAGT[A/G]AACAATTCAGTGGCA | 90293 |
rs756529805 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074540 | CTGGCTGGAGCAAGA[C/T]AGGGTAAATACCACA | 90293 |
rs756531793 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093959 | GAGCGACACAGAAGA[C/T]GGGTAATTTCTGCAT | 90293 |
rs756533157 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117994873 | CTAGCCTGGACAACA[C/T]AGTGAGACTTCATCT | 90293 |
rs756533467 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118068274 | ATGGGTAGAGAGGAA[A/G]ATGGCCGACTAGAAG | 90293 |
rs756534471 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953321 | AAAAAACCAAACACC[A/G]CATGTTCTCACTCAT | 90293 |
rs756534814 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950219 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA | 90293 |
rs756544119 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076960 | CACCCCTTGATAGAT[-/A]AATCTCCTAATGGTT | 90293 |
rs756546019 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117969076 | GACTAAAGGAGAACA[-/AT]AGTCTAGTTCACTAA | 90293 |
rs756554513 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117904220 | ATTTAATTTTTATTG[A/T]CAACTTTTATTGTCA | 90293 |
rs756571098 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118100304 | AGCTGCTACCACGTT[C/T]TCAGTTACTTCTGGA | 90293 |
rs756572452 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014419 | GGTAAATTCTAGTCA[G/T]ACCAGTTCTCTGCTC | 90293 |
rs756593621 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118020608 | AGGGATCTAGAACTA[C/G]AAATACCATTTGACC | 90293 |
rs756598426 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076131 | ACAACAGTTTTTGTC[C/T]CTTCTATTTCTTCTT | 90293 |
rs756600396 | in-del | -/GA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903182 | GAGAGAGGAGAGCGA[-/GA]GAGAGAGAGAGAGAG | 90293 |
rs756613780 | snp | A/C | 0.123679 | 0.215738 | intron-variant | KLHL13 | GRCh38.p7 | X:118036484 | CCGGAGAAAAACAAG[A/C]AATGGGGAAAGGATT | 90293 |
rs756622568 | snp | A/G | 4.58679e-05 | 0.00478872 | intron-variant | KLHL13 | GRCh38.p7 | X:117920388 | ACAACAAGAACATGA[A/G]TTGAGTCACTAATCA | 90293 |
rs756649699 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970223 | TTCAATGAAAACCAC[A/G]TAATGTATATTTGAC | 90293 |
rs756657435 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030763 | CCTTCCAACTTCTGC[C/T]ATGGGATGACACAGC | 90293 |
rs756663766 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117925881 | GTTTTGTAGAGAAGG[A/G]GTTTCATCATGTTAC | 90293 |
rs756674577 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113949 | GAATGATACATAAAA[A/T]CCTGATTGTTATGAA | 90293 |
rs756681806 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118021128 | CACATGTACCCTAAA[A/G]CTTAAAGTATAATAA | 90293 |
rs756685689 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040688 | ACCTAGAGAAAGATA[A/T]CAATATTCAAGTATA | 90293 |
rs756699416 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118112502 | AAAAGAAAGGCATGG[C/T]ATCCATTTGACAAGC | 90293 |
rs756700871 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086525 | TGTGAATTATATCTC[A/T]ATTTTTTTAATTATA | 90293 |
rs756705547 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118031830 | TTCCATCTGAGGTAC[C/T]GGGTTCATCTCACTA | 90293 |
rs756705667 | snp | A/G | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118037488 | TCTCAGTAAACTATC[A/G]CAAGAACAAAAAACC | 90293 |
rs756720947 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948368 | CCTAACAGAATATCT[C/G]TGCTCTCCACAGGCC | 90293 |
rs756723058 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057207 | CGTGTCTATGGTTAA[C/T]TATTTTCCATAAGTG | 90293 |
rs756728772 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117903402 | TTTACCTACTGCTTT[C/G]TTGGCTTTGTTCATT | 90293 |
rs756730544 | in-del | -/TAAT | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118058326 | TTCTCTTACACACAC[-/TAAT]TAATTAAAGTATGCC | 90293 |
rs756789352 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117957979 | TGATGAACCATGACT[A/G]AAGTATTTTGGTCAC | 90293 |
rs756795069 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104780 | TTTGTTTCAAAACAA[A/G]TTTCTCTTTCTGAGG | 90293 |
rs756795490 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079537 | GAACACAATCGTATT[C/T]ACAATAGTCACAAAG | 90293 |
rs756797059 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118032069 | CAGGAGATTATATCC[A/C]GCACCTGGCTCAGAG | 90293 |
rs756808466 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117987876 | TTATAAGGAAAAAAA[A/G]CAAGTACAGAATAAG | 90293 |
rs756812699 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935922 | ACAATTGATTGTGGT[C/G]ACAGTTGCACAATCC | 90293 |
rs756820422 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007747 | GGCCTCAGGAAGGGA[G/T]GAGGACACATTGCCC | 90293 |
rs756823682 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117916726 | ATGATTGAGAATAGG[A/G]TAGAACAGAATTGTA | 90293 |
rs756834546 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118024069 | AAGACTCAAAAGTCA[C/T]TGTGTTATAAACTAG | 90293 |
rs756839694 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097301 | CAGACAAACAGAGAA[C/T]CAGATCATGAGGGAA | 90293 |
rs756849937 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025099 | CAACATCCCCTGATC[C/T]ACTCCTGTTTTCACC | 90293 |
rs756865620 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917216 | CTACTCTAAAACCAT[A/G]CAGACATATCCTCTG | 90293 |
rs756867633 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107895 | TGTCTCTACAAAAAA[C/T]ACATAAAATTAGCCA | 90293 |
rs756871878 | snp | A/C | 2.28201e-05 | 0.0033778 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909605 | CAATTCCTTACTGAC[A/C]ACCAGCTGCTGCCTC | 90293 |
rs756875088 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076247 | TGTTCCAGGATTGAG[G/T]TTTATTTTGAAATTA | 90293 |
rs756881052 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118105030 | TTTTAACCTCTAAAG[-/T]TTTTTTCCAGTTTAA | 90293 |
rs756890461 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041058 | ATCTGTCCTAGAAGA[A/C]ATGCTAAAGGGAGTT | 90293 |
rs756895704 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968917 | ATACACAATATTTTC[C/T]CAGGAAATGCCAGGT | 90293 |
rs756900589 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933880 | ACTAACTCTGCTTGG[G/T]TCAAGAAAAGTTTAA | 90293 |
rs756900732 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004217 | TTGGTGAGAACTCAT[A/G]GTTTCAATGGATAAA | 90293 |
rs756940242 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072974 | TGGTGAGTGCCTCTA[C/T]TGCCAGCTACTCAGG | 90293 |
rs756944248 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991921 | CCCCCTCCCACATTG[A/T]TTGCTCTGTACCAGT | 90293 |
rs756945779 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118068264 | GAAAAGCACAATGGG[C/T]AGAGAGGAAGATGGC | 90293 |
rs756957417 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023700 | CAGCCTCCCAAATAG[C/G]TGGAATTACAGGTGT | 90293 |
rs756968882 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981555 | ATTCTGAAGCTACAT[G/T]TTCCCTTTAGCTAGC | 90293 |
rs756997113 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962618 | ACCACTTGACAGTAA[A/G]CAAGTAAAGCTTTCT | 90293 |
rs756998384 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050754 | ATGTAATCCACTGAG[C/G]CCTGATACACACACA | 90293 |
rs757001763 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117908668 | GACCAATTTTATACT[C/G]GGAAGACAAAAAGGT | 90293 |
rs757004926 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974170 | TTCTAAAAAGTGAAT[A/G]TAGGTTAAATGAGTA | 90293 |
rs757017814 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944087 | TCTAACAGGCCCCTC[A/T]GCTGCAGATCTGCTA | 90293 |
rs757021647 | snp | A/G | 4.61388e-05 | 0.00480284 | intron-variant | KLHL13 | GRCh38.p7 | X:117920413 | TAATCAAGGTAAAAT[A/G]AGGTTACAAATCTTC | 90293 |
rs757031535 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117925822 | CCTGGAATATCCTTC[C/T]TCCTTCAAAGACTAG | 90293 |
rs757043505 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117931997 | TTCTCTATCCCAGGG[A/C]TAAGCTCTTTATATG | 90293 |
rs757044616 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073308 | GGAAGTCACATCATA[C/G]ATGGATGGCAGCAGG | 90293 |
rs757045688 | in-del | -/GAGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903180 | GAGAGAGAGGAGAGC[-/GAGA]GAGAGAGAGAGAGAG | 90293 |
rs757050967 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924462 | AGATTCCTGCACACT[C/T]GAAATAAGTCCTTTT | 90293 |
rs757053978 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041796 | TAAAGGAAGACAGGA[A/G]GGAAGGAAAGGAGGA | 90293 |
rs757054874 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922487 | AAATTTTACTCAGAA[A/G]CTACCACTGGTAACT | 90293 |
rs757063401 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117941574 | TCTTGGGAGGGTGTA[C/T]GTGTCTAGGAATTTA | 90293 |
rs757067071 | in-del | -/T | 0.138694 | 0.223855 | intron-variant | KLHL13 | GRCh38.p7 | X:117992597 | TTGCTAAGGCTGGGC[-/T]TTTTTTTTTTCCTTT | 90293 |
rs757067485 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994162 | TTAAGTTGGGGTTTT[A/G]TTTGCACTTGTACAT | 90293 |
rs757068509 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118116228 | GGAGAGATGACAAAG[A/C]AGCACAGGAAAGCCG | 90293 |
rs757069477 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118777 | TGCTTTATCTGAATA[C/T]TTAATCTACTGGATA | 90293 |
rs757091399 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117954208 | ATTTGCTCCCTCTGC[G/T]TACCATATTTCAAGA | 90293 |
rs757132578 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065969 | ATATTATCTAAAAAT[C/T]TGTAAAGTCATAACA | 90293 |
rs757132808 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996226 | AATACAAATTTCAAA[C/T]ACTTTCATCAAATTT | 90293 |
rs757151898 | in-del | -/A | 0.357306 | 0.2258 | intron-variant | KLHL13 | GRCh38.p7 | X:117983436 | AACCAATTCGCACTG[-/A]AAAAAAAAAAAAGGT | 90293 |
rs757164193 | in-del | -/AATAA | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118054348 | CTATATCTCTAATAT[-/AATAA]AATATTATTAAGTTC | 90293 |
rs757166244 | snp | A/G | | | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898656 | AGAAACATTTTATAG[A/G]CAATACTTTTTTTTT | 90293 |
rs757207209 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038119 | GTGTCTAACAGAAAA[C/T]TGAAAAGATTACATC | 90293 |
rs757219033 | snp | C/T | 0.000164491 | 0.00906744 | missense | KLHL13 | GRCh38.p7 | X:117898954 | GGTGATGGTGTGGTT[C/T]CTTCTGGTGGAAAAA | 90293 |
rs757220588 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084172 | AAAAAAAAAAAAAAT[A/G]TTTAAAAACTTAGCT | 90293 |
rs757221592 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118102058 | GGAAGTCCAAGTAGT[C/T]CCCATAAGGCTGCAA | 90293 |
rs757228893 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118012915 | GACTTGTCTCTTCTA[C/T]CCTACTTATTTATTC | 90293 |
rs757245335 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109071 | TGCTCCCGCCTAGGC[A/G]TCCCAAAGTGTTGGG | 90293 |
rs757245432 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013607 | TAAACCAATGTGACA[A/G]ACAAAATGTACATTA | 90293 |
rs757246924 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942652 | ACTAGGATTGCAACC[C/T]CTGCTTGTTTTTTGT | 90293 |
rs757248174 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030059 | AGGAGGGATTCTTCA[C/T]TGTCGTCAGCCCTCT | 90293 |
rs757251978 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066699 | AAGAAAATGAAAGGA[A/C]AAACCACAAACCAGG | 90293 |
rs757285181 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117914454 | TACTTGGTGCTATCT[A/G]GTTTATTAAAATGAC | 90293 |
rs757289695 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027474 | CACTTAAAAAAGCAA[C/T]TTGATTTGGGTGGAG | 90293 |
rs757300724 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015266 | AATGTATCAGAAGAC[C/T]AGAGTGAAAATACAT | 90293 |
rs757304738 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077084 | CTCTTGGCTTGGTGC[C/T]TTCTGGAATCATGTG | 90293 |
rs757311737 | in-del | -/AGGAAGGAAGGAAGGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930247 | GGAAGGAAGGGAGGA[-/AGGAAGGAAGGAAGGA]AGGAAGGAAGGAAGG | 90293 |
rs757312709 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997780 | ACCCAGCACATTCAG[C/T]CTTGTCTAATAATTC | 90293 |
rs757318018 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117946396 | AATAGGAGAACCTTA[C/G]TCAGTAGGTCACTTA | 90293 |
rs757320583 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118005052 | ACAATTAATTGCAAT[A/G]CATAATTCTGAAGTT | 90293 |
rs757329184 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103540 | CGGTAAAATTAAAAG[C/T]AAGAAAAATTGTAAG | 90293 |
rs757331051 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016061 | TCCAATGGCTGATCA[A/C]CTTGTTAAATTTGTT | 90293 |
rs757341726 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955752 | TCCCTTTTCTGCATA[A/T]CTGCCTCACCATTAA | 90293 |
rs757354079 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911600 | TTCCCCTCCCTGTGC[C/G]CATGAGTTCTCATTG | 90293 |
rs757354583 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118095623 | ACACCTATTCCAAAA[C/T]TGACCACATAGTTGG | 90293 |
rs757359739 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910537 | ACCACACAGCTAGCA[C/G]ATCCATGAACAGAAA | 90293 |
rs757364040 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100920 | TCATTTCTATTCCTT[C/T]GGCAATTTTTTCTCA | 90293 |
rs757379525 | in-del | -/GGCACAAGACA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965990 | TTCCCTTTGAAAACT[-/GGCACAAGACA]GGGATGCCCTCTCTC | 90293 |
rs757406526 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118077811 | TCACAATTGTATTCA[C/T]AGTCATAGGGGCTTG | 90293 |
rs757433130 | snp | A/G | 3.29576e-05 | 0.00405928 | missense | KLHL13 | GRCh38.p7 | X:117909337 | GCCCACCAACTGCAT[A/G]CAGATATCCTTTGAG | 90293 |
rs757436308 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089046 | GGATCAGAAAAAGGG[C/T]AGAATATTAGGACAG | 90293 |
rs757440158 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118070726 | GATTTGTCATTTTCT[C/T]TTTTTTAATTTTTAA | 90293 |
rs757442473 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096178 | AAAATTGATAGACTG[C/T]TAGCAAGACTAATAA | 90293 |
rs757444345 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998480 | AAGTAAAGAGATTCT[A/T]AAAAAAAACACAAGA | 90293 |
rs757474394 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954070 | TATGACGTAGATAAG[A/G]GAATTGGGCTAGACA | 90293 |
rs757494991 | snp | A/G | 2.28838e-05 | 0.00338251 | missense | KLHL13 | GRCh38.p7 | X:117901935 | TTCTTGGATTGTAAC[A/G]TTCTACTGTGGCTGT | 90293 |
rs757504449 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117966788 | GATCTTTGACAAACC[G/T]GAGAAAAACAAGCAA | 90293 |
rs757524503 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939100 | CCCCTAGCCCCCCAC[C/T]CCCTGAAAGGCCCTG | 90293 |
rs757524968 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047636 | CCAACCATAATAGAA[A/C]CAGGAAACAAATAAA | 90293 |
rs757527037 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025859 | CTGCTGTCACACTCA[A/C]ACTGCAAAAGTTATG | 90293 |
rs757535986 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118062636 | ATCCTGAAATACGTA[C/T]AGTTTCACTATAAAT | 90293 |
rs757546312 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902114 | TACAGTAATTATTGA[C/G]ACTATATTAATAATA | 90293 |
rs757556223 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032400 | TGGAGATCTGAGAAC[A/G]GGCAGACTGCCTCTT | 90293 |
rs757567066 | in-del | -/GAG | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117989515 | TAAATGGCTGGAGGA[-/GAG]GAGAAGTAAGGAATA | 90293 |
rs757569057 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117975997 | TTGGGCTCCAAAGAA[A/G]CTATCTAATACCATG | 90293 |
rs757579585 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040457 | CTCTCAACAGTAGAA[C/T]TGATAAAACATGAGA | 90293 |
rs757583762 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118009144 | CATTGTAGATTCTGG[A/G]TATTAGCCCTTTGTC | 90293 |
rs757590442 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118051819 | AATCTGTAGTTCATT[G/T]GGAGAACTGAACACA | 90293 |
rs757599620 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117952134 | AAGCTGGAGGCATCA[C/G]GCTACCTGATTTCAA | 90293 |
rs757602532 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921152 | TCAACTAACGACAAA[C/T]AGACAGTTGTTCTAT | 90293 |
rs757618301 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117988422 | AGGATGACTTAAGTG[A/G]TTTACAGAATTTTCT | 90293 |
rs757624714 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117951460 | AAAGAATATATCTTC[C/T]TAATGAGGTGTTTGC | 90293 |
rs757635546 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117919127 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 90293 |
rs757635910 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118106192 | ATGAGCCACCGCGCC[C/T]GGCCAAGAGCTTTTT | 90293 |
rs757645898 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118032682 | TCTAAAAAGCAGAGC[A/G]CCTCTCCTCCTCCAA | 90293 |
rs757659711 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112375 | TGGCCAGGCATCAAA[C/T]AAGCATAATTATGAC | 90293 |
rs757670533 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968682 | AATTTAATAAGTATT[G/T]TGCTAGAAAAGAAAG | 90293 |
rs757677455 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903838 | ACACTTTTCTTAATG[C/T]GGGACTCTGACTTAA | 90293 |
rs757680051 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118043095 | CAAAGGATCATTACT[A/G]GCTACTATGAGCAAA | 90293 |
rs757690459 | snp | A/G | 6.89132e-05 | 0.00586957 | intron-variant | KLHL13 | GRCh38.p7 | X:117919512 | AAATCAGATTTCAAA[A/G]TATCTTACCCCAGAT | 90293 |
rs757691597 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002454 | CAAAATTAGCCGGGC[A/G]TGGTGCTGCATGCCT | 90293 |
rs757691637 | snp | G/T | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118020146 | AATGTTCTTCCATTT[G/T]TTTGTATCCTCTTTT | 90293 |
rs757700547 | in-del | -/AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118052521 | GCAAGACTCCGTCTC[lengthTooLong]AAAAAAAAAAAAAAA | 90293 |
rs757715851 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117964386 | TGTTTGTCTTGGTTC[A/C]AAATTTTCACAGCAG | 90293 |
rs757723296 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117971628 | GAAATGGCCTCATTT[G/T]TCAACACTTTCCAGG | 90293 |
rs757725547 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117946489 | TGCCATTATTAATAA[A/C]CTTTCATCATTCCTT | 90293 |
rs757725618 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970016 | TATTGTAGCCTTCAC[C/T]AGCACAGCAGTACTG | 90293 |
rs757729683 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118107287 | AATGTGATGCCATAT[A/T]TGAGTAAGTAATAAG | 90293 |
rs757730215 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039595 | CCAGGTAGATTCCTA[A/G]GGTTTCCGACTCTAG | 90293 |
rs757732851 | in-del | -/TAT | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118082452 | CCAATTTTTTAATCA[-/TAT]TATTTTCTTTTTTGC | 90293 |
rs757771053 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986868 | GAAATCTTTTTGATC[C/T]TTTGCCCACAAAATA | 90293 |
rs757771655 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118027627 | CACACCCGCTCTCTA[-/T]TTTTTCTCTCTCTCC | 90293 |
rs757776468 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117972135 | TACTTTTTCAATCCC[C/T]ATAATATAACTGCTC | 90293 |
rs757790463 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043577 | GGGATGCAAGGATGG[C/T]TCAACATACATAAAT | 90293 |
rs757804041 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117901482 | AAAATCAACATAAAT[A/T]ATATTTTGATTCTCC | 90293 |
rs757809552 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059516 | CGATTTGGGGGCTTA[C/T]TAGGAAATTTCACTC | 90293 |
rs757818821 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075299 | GTTTATGTGTAACTC[-/A]AAAAAAGATTTTTTT | 90293 |
rs757819701 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118099660 | CTCTAATAAAAATTT[A/T]AAAAAAAATTAGCTG | 90293 |
rs757823815 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117993907 | ACGCCCGGCTAATTT[C/T]GTATTTGTAGTAGAG | 90293 |
rs757835031 | snp | C/T | 2.28922e-05 | 0.00338313 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117919665 | TTTCCTTAGACCGAC[C/T]TTGCTCACACCATGA | 90293 |
rs757862559 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060715 | AAAATCTGAACTGCA[A/T]CCACTAAATTATACT | 90293 |
rs757863240 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094242 | GAAATATGTGACGAA[C/T]GCACAAGCCTCAGTA | 90293 |
rs757863398 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020539 | ACACTTTTACACTGT[C/T]GGTGGGACTGTAAAC | 90293 |
rs757869593 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076164 | TTAATAAAGTTAAAC[C/T]GCAGTTTCAGTTGAG | 90293 |
rs757878711 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118067157 | ACAGGCTACAAACCT[C/G]TAATGCATGTGACTG | 90293 |
rs757889655 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914561 | GTACTTCAGCAGGCA[A/G]AGAATGTACAGGTAT | 90293 |
rs757902370 | snp | G/T | 0.113499 | 0.209446 | intron-variant | KLHL13 | GRCh38.p7 | X:118036231 | CTTTCTTCACAGAAT[G/T]GGAAAAAACTACTTT | 90293 |
rs757908937 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981220 | GCACATGCCACATCA[A/T]GTGTTCATGTGTTGT | 90293 |
rs757918968 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117964936 | CATTTTTTATGGCTG[C/G]ATAGTATTCCATGGT | 90293 |
rs757932570 | in-del | -/AAAT | 0.159114 | 0.232894 | intron-variant | KLHL13 | GRCh38.p7 | X:117999708 | TAAAAAATCTATTAA[-/AAAT]AAATAAATAAATAAA | 90293 |
rs757938258 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911516 | CAACCCGTCATCTAC[A/G]TTAGGTATTTCTCCT | 90293 |
rs757945023 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086467 | TGAACATACTAAAAA[A/G]AAACACTGATTTGAA | 90293 |
rs757947333 | snp | C/T | 2.54307e-05 | 0.00356577 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972863 | AATAACAGTAAAGAG[C/T]GTTTCCATAACAGAC | 90293 |
rs757952420 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027650 | TCTCTCCACACATAC[-/AC]ACACACACACACACA | 90293 |
rs757958298 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925076 | GATAAATTTTAAAAT[A/G]ATCATATTAAAACAG | 90293 |
rs757971232 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118103849 | TAGCTGAAAAGTCAG[C/T]GGCCGAATTTTTTTT | 90293 |
rs757974210 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117956910 | TTAATGGTAATGAAT[C/T]TGACTACATACATAT | 90293 |
rs757999830 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118031729 | ATATTTGAAAATTAG[C/T]GGAGGGAGCCAAGAT | 90293 |
rs758003237 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079045 | ATCATCTAAAAATAA[A/G]AGACAATCAACAAAG | 90293 |
rs758006505 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977027 | AAACTAGAAACCAAA[-/T]TTCAATCTCCTAGTA | 90293 |
rs758011202 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925784 | CTCCAAACGATCACA[C/T]TGGTGATAAAAATTT | 90293 |
rs758016567 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074480 | CAGGAAATTTTCCAT[A/G]GATGTCCCCACTCCT | 90293 |
rs758017366 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118006863 | TCAGGTAAATAAACT[A/G]CCCTTAAAGGGAAAT | 90293 |
rs758023577 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092592 | ATAAAAGAGGGTATC[A/T]TGGAACATCAGGAAG | 90293 |
rs758031645 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118112328 | GGATGAGGTCTAGGT[C/T]GCCTTCATGAAGCCA | 90293 |
rs758034698 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999238 | GCTATAAAGACGCAT[A/G]CACACGTATGCTTAT | 90293 |
rs758049063 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978037 | TGTAGTCTTGCCACA[A/G]TAAAAAATGGAAAAT | 90293 |
rs758054351 | snp | C/T | 2.46393e-05 | 0.00350985 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898867 | GAATTTATGACACAT[C/T]GCAAAGATAGAACTA | 90293 |
rs758059655 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018026 | ATAATGCATGCATGA[C/G]GATGTTCAGATAAGT | 90293 |
rs758062952 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948078 | CCCCATGATTCATAA[C/T]GTCTGCAGACATTTT | 90293 |
rs758069221 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118058054 | GAAAACATGAAGTTA[C/T]CCAATGTCAAAATAG | 90293 |
rs758079545 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117916619 | TAAAACTAATACATA[C/T]ATGTTTTCTAGGTTC | 90293 |
rs758091194 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118079367 | TCCCTCTTTGCTGAT[A/G]ATATAATTCTATTAT | 90293 |
rs758094123 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968655 | AACATTCTTTTCTAT[A/T]TTGAGATTATCAATT | 90293 |
rs758138470 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023346 | TATAAGTGCAAGTTT[A/C]TGTCACTAATCTTTT | 90293 |
rs758143501 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118104652 | GCAATTTGGAGCTAG[A/T]CTGCAGAAAAACAGC | 90293 |
rs758150905 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117948198 | GCCAAAGGTGAGAAA[A/T]CCTAATATAGAGGAA | 90293 |
rs758162177 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907463 | AGAAAAGAAGACTGA[C/G]CAAGTTAATGACCTG | 90293 |
rs758178572 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117941284 | TGTTGATCAGCGATA[G/T]TGGCCTGAAATTTTC | 90293 |
rs758184133 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085169 | AAACATAAGTAGTAG[C/T]ATATTCATACCTTGT | 90293 |
rs758185030 | snp | A/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:118071850 | CAAACAAATGGAAGA[A/T]CATTCCATGCTCATG | 90293 |
rs758187987 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117930669 | GGAAAGCGGCAGACA[A/G]TCTTCCAACTTTTAT | 90293 |
rs758197897 | snp | A/C | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118096782 | GTTCAATATACGCAA[A/C]TCAATAAACGTAATC | 90293 |
rs758200304 | snp | C/T | 0.000168876 | 0.00918747 | intron-variant | KLHL13 | GRCh38.p7 | X:117983590 | TTAATTGTAGTTTTA[C/T]TATATTTAGTTCAAA | 90293 |
rs758206106 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117949582 | CATTTGACTCAAAAG[C/T]CACAAATAATCTTCC | 90293 |
rs758209105 | in-del | -/G | 0.294752 | 0.245962 | intron-variant | KLHL13 | GRCh38.p7 | X:118053844 | AGAGAGAGAGAGAGA[-/G]GAGAGGAGAGAGAGA | 90293 |
rs758243987 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000266 | CACAGAATCCTAATC[C/T]ATCACTGGGAATTGT | 90293 |
rs758260189 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117493 | CCTAATTCACAGCTA[C/T]TCTACAAGTTACACA | 90293 |
rs758270793 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072811 | TGTCAAATGGAGAAA[A/G]AGGCTGGGCATAGTG | 90293 |
rs758270796 | in-del | -/AA | 0.000695652 | 0.0186371 | intron-variant | KLHL13 | GRCh38.p7 | X:117983436 | AACCAATTCGCACTG[-/AA]AAAAAAAAAAAGGTG | 90293 |
rs758278989 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961876 | TTTTATTTTAGCCCC[A/G]TGAGACCAGTACCAA | 90293 |
rs758279416 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015107 | ATGGACTCATAGGAG[A/T]TAAGACACTTTCCAA | 90293 |
rs758284246 | snp | C/T | 2.28193e-05 | 0.00337774 | missense | KLHL13 | GRCh38.p7 | X:117909586 | CCTTTTCATCATACA[C/T]GCGCAATTCCTTACT | 90293 |
rs758287563 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097261 | TCAATGTGCAAAAAT[A/C]ACAAGCATTCTTATA | 90293 |
rs758295024 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916020 | AAAATTAGCCAGGCA[C/T]AGTGGTGCATGCCTG | 90293 |
rs758296947 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064240 | TCTGATTTTTCACTT[-/A]AAAATGTGTTTTTGA | 90293 |
rs758297647 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026328 | CAAAATGTGTATTTT[-/G]AAAAAAACTATGCAT | 90293 |
rs758300817 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118105701 | AGTAGAGTGCTTTAC[A/G]TATAATTGCTTGTTC | 90293 |
rs758309218 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969710 | TCATCAATCAATCTA[A/G]AGACTGAAGTATTAT | 90293 |
rs758318520 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118024683 | TGAAAACCATAATGA[A/G]GAAGTACTACACACC | 90293 |
rs758324045 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108246 | CGATAAAGACCATCC[A/T]CTAATCACAATCCTC | 90293 |
rs758329051 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118083586 | GCTGGGCGAGAGTGG[A/G]GGGCAGGTAATGAAG | 90293 |
rs758341890 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117908609 | ATTTTACCTTTTTGG[A/G]TTAATTTACATAGCC | 90293 |
rs758346385 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118033186 | GGATATTATCCAGGA[C/G]AACTTCCCCAATCTA | 90293 |
rs758353561 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118012278 | CAAATGATCACAAAT[A/G]GTGGCTTTAAACAAC | 90293 |
rs758356119 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118011721 | AAACAATACCAAGAA[C/T]ATAGATGACAAGGCA | 90293 |
rs758360160 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083296 | CTCGTGTTTACTGCA[A/G]CACTATTAACAATAA | 90293 |
rs758360296 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953444 | GCATTAGGAGATACA[A/C]CTAATGCTAAATGAC | 90293 |
rs758385305 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118053328 | AAAAATGATGAGTTC[A/G]TGTCCTTTGTAGGAA | 90293 |
rs758408501 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046053 | AATTACAAACCCCAA[A/C]GAAAGAAAATCTATG | 90293 |
rs758415287 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118076333 | CACAAGATAAATTAT[A/T]ATACACAATTGGGAT | 90293 |
rs758415899 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959760 | ATGATGTCAAGGTCT[C/T]ATCTCATTGATCAGT | 90293 |
rs758432771 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028948 | CACCTGGGATGTAAA[A/T]CATCCTTTTGTGCAG | 90293 |
rs758444002 | snp | A/G | 2.28428e-05 | 0.00337948 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117901897 | GGGCTCACTCATTTT[A/G]GCAACATAGGTCCAT | 90293 |
rs758444209 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117945355 | ACAACCTCCTCCACT[A/G]CTGACATCCTGCATC | 90293 |
rs758451940 | snp | A/G | 0.00105904 | 0.0229869 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897595 | GAAAAGCCAGTTAGC[A/G]TCTTCCATAATCTAA | 90293 |
rs758456188 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118021300 | AATGTGCAGGTTAGT[C/T]ACATATGTATACATG | 90293 |
rs758458714 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922255 | GCAGTGGCGCGATCT[C/T]GGCATTGATATATGG | 90293 |
rs758472603 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117923060 | TTCTTTTAGTGCATG[A/C]ACAGTAATCTACAGT | 90293 |
rs758474280 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982629 | AAACATTAGTGTGCA[C/T]AAGAATCACATGAGG | 90293 |
rs758500494 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101441 | GAGAGAGACAGAGAA[G/T]GAAAAACACTACTTG | 90293 |
rs758502627 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117953922 | TTCTCCCAACACTTA[C/T]GGGGTAGGGAGGTAG | 90293 |
rs758514560 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029457 | GTAGGAAAAGAGTAG[C/G]TGAGTTTTGGTAAAC | 90293 |
rs758518895 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046927 | AGTGGTGACCTTTAC[C/G]AAGAGCAGTTTCAAT | 90293 |
rs758527180 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973547 | AGGAGAAGGCAAAAT[A/G]TAAGAAGAATATAAA | 90293 |
rs758553989 | in-del | -/CT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084145 | AGCAACATAATGAAA[-/CT]CTGTCTCTACAAAAA | 90293 |
rs758554321 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107877 | AGCAACATGGTGAAA[-/C]CCTGTCTCTACAAAA | 90293 |
rs758565428 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055745 | CAACACAGCAAGACC[C/T]TCAGCTCTAAGAAAG | 90293 |
rs758574935 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118035064 | TTGAATCTCTGAATA[C/G]ACCAATAACAGGAGC | 90293 |
rs758593522 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118101966 | TCCAGTCTTGGGTAT[C/T]TCTTTATAGTAGTGT | 90293 |
rs758593747 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100753 | TCACTCAACTAAAGA[C/G]ATCTCAAAATTCTCC | 90293 |
rs758595482 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913602 | TGTAATCCCAGCACT[C/T]TGAGAGGCCTTGGTG | 90293 |
rs758596361 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077031 | CATACTTTTGCTTTA[C/T]TATTGTATTTTGCTT | 90293 |
rs758601069 | snp | A/G | 2.68716e-05 | 0.00366539 | intron-variant | KLHL13 | GRCh38.p7 | X:117945605 | ACATAAGAAAGAAGG[A/G]GAAATTAAAACTTGT | 90293 |
rs758603784 | in-del | -/AA | 0.113744 | 0.209605 | intron-variant | KLHL13 | GRCh38.p7 | X:117996831 | AATCATAGCCTATTT[-/AA]AAAAAAAAAAAAAGC | 90293 |
rs758611141 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118095568 | TACAGAACTCTCCAC[C/T]CCAAATCAACAGAAT | 90293 |
rs758613489 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117972378 | ATCATCAATTTTTAA[C/T]GCCATTACACAAAAG | 90293 |
rs758625081 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004842 | CCTGATAGGATGCAA[C/T]GAGAAGATCATGTCT | 90293 |
rs758630806 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114447 | GGCAAATATAAATAG[C/T]CTTACTATGCAATCA | 90293 |
rs758655926 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117965856 | ACAAAATTCAACAAC[C/T]CTTCATGCTAAAAAC | 90293 |
rs758657441 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974556 | CTACAGTAAGGAACT[A/C]TTTTCAAAAATTCCA | 90293 |
rs758658937 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117988234 | AGAAAGGGAGGAGGG[G/T]TAACTACCTCTTGGA | 90293 |
rs758664105 | snp | C/T | 2.32699e-05 | 0.00341092 | missense | KLHL13 | GRCh38.p7 | X:117899360 | CAGGGTCAAAGCACA[C/T]GAGCTCCTTTTGGAA | 90293 |
rs758666148 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117946344 | TTCTGTATTTGCATG[C/T]ATTGCAGCAATAGTA | 90293 |
rs758701954 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118046433 | GGGATGGTTAATGAG[C/T]ACAAAACTACAGTTA | 90293 |
rs758707148 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088863 | GCAGGAAGAAGCAGA[C/T]GGGCTAGGGACCTCA | 90293 |
rs758715612 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118016571 | TTGCATTATGTACAA[C/T]ACAGGATATAAAAAT | 90293 |
rs758719215 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117938507 | ATTCTGGTTTGGGAC[C/T]TAGCGTTCAGTGTTT | 90293 |
rs758722010 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904905 | AGAATCTCTCCAATT[G/T]AAGAATTATACTTAG | 90293 |
rs758731170 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059439 | CCTAAAGCTATATCA[A/T]TCATCTTAACCCTGC | 90293 |
rs758737562 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007103 | GAGTAGCCTCCCAAG[C/T]TTGAGAAGTCAAAAG | 90293 |
rs758758843 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060218 | ACTGTGTCTTAAAGG[A/G]AGTTATGTAAGCAAA | 90293 |
rs758762418 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117979662 | GCTATTACCAAAAGC[A/G]GAGGTCAAGAGGGAT | 90293 |
rs758776614 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118051116 | CATGAAAACAAGGAT[C/T]TCTTATATTCCACCA | 90293 |
rs758782073 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113537 | AGTCTCTTTTTCCCC[C/G]CTCAAGGCCTTGGCT | 90293 |
rs758791372 | snp | A/C | 2.90943e-05 | 0.00381396 | intron-variant | KLHL13 | GRCh38.p7 | X:117910137 | AAACATGACTACTTT[A/C]ATGGCAATCACATCT | 90293 |
rs758817775 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118026073 | ACAAACAGGCACCCA[A/T]CATGTTATTTCTCTA | 90293 |
rs758821757 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025724 | CATCCTGCACATGTA[C/T]CCCAGAACTTAAAAC | 90293 |
rs758837093 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967489 | TGTATGAAATTCTCA[C/G]TAACTCCGTACTTCC | 90293 |
rs758838572 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117936531 | TTTAATTCATTAACT[A/G]TTTTCTGTTTTCTTC | 90293 |
rs758840757 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955453 | TGTATTCAAAGCCCG[C/T]AATAAATTTACCAAA | 90293 |
rs758864710 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005640 | AGCACTGCTGGCTTC[A/G]AAGATGGAGGAAGAG | 90293 |
rs758868389 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109356 | AATGTTTGGGTGTTT[A/G]ACTAAAAGAACAGAT | 90293 |
rs758871719 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118114415 | ATGGCTAACTCATCC[A/G]CCTTTATTCTTTTCC | 90293 |
rs758902740 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118107146 | TGTTCATAGTATACA[C/T]TATCCTGCATAACCC | 90293 |
rs758903258 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927438 | TGTGGTGAATATTCA[A/G]TTCAGTTCCTCTCTC | 90293 |
rs758935613 | snp | A/G | 6.84307e-05 | 0.00584899 | missense | KLHL13 | GRCh38.p7 | X:117919591 | CTGGCAGCTTCCAGC[A/G]TGTCTTGAAGGTTGT | 90293 |
rs758936285 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081047 | TTGTTACTTAGAAGT[G/T]GGAGCTAAACATTGA | 90293 |
rs758940024 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981189 | AATTAAAATCCTATG[A/G/T]TGTACAACATCATTA | 90293 |
rs758950986 | snp | C/T | 2.43721e-05 | 0.00349077 | missense | KLHL13 | GRCh38.p7 | X:117910039 | CGTATTTATCCACTT[C/T]GGTTAGATTGTAGGT | 90293 |
rs758957604 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118032597 | CCCATCTGTACATCA[A/C]CATCATCAAAGACCA | 90293 |
rs758962266 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118082339 | ACTGTGGTTCTGATT[C/T]GCATTTCTCTGATGA | 90293 |
rs758965077 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001040 | GAACAAGCAAAAAGT[A/G]TAAAGAACAATCTCA | 90293 |
rs759003535 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080051 | CTCCCTATTCAATAA[A/G]TGGTGCTGGGATACT | 90293 |
rs759017542 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027456 | TTAAATGGCTGGTAT[C/T]AACACTTAAAAAAGC | 90293 |
rs759024099 | in-del | -/AA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073725 | ACTTTCTAACAATAT[-/AA]AAAGTTGGCTACCCA | 90293 |
rs759024972 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117952030 | GCTACCAATGACTTT[A/C]TTCACAGAATTGGAA | 90293 |
rs759031848 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117953095 | ATGCTGCTATAAAGA[C/G]ACATGCACACGTATG | 90293 |
rs759034679 | in-del | -/AAAT | 0.32941 | 0.237053 | intron-variant | KLHL13 | GRCh38.p7 | X:118002596 | GAAACTCTGTCTCGA[-/AAAT]AAATAAATAAATAAA | 90293 |
rs759048847 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118116739 | AAAGTCCCCGTTCCA[C/G]GCTTCCCAGGAATAG | 90293 |
rs759049701 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041727 | CTCATATCAAAAAAC[A/G]TATATCAGATATATA | 90293 |
rs759063101 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117930084 | TTCACCATTTTTCTA[C/G]AGGTTTTATCCAGTG | 90293 |
rs759063626 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118019252 | TGACATTTACAAATA[A/C]AGTATTTTCATGTGT | 90293 |
rs759066342 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117972026 | GCAAATTTAAAAAGA[C/T]TTTCAAAAATTTTGA | 90293 |
rs759078293 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922377 | AGTCAAGCATCAGCT[C/G]AAACAGTTGAGAGAC | 90293 |
rs759080113 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118090726 | TCAGTGTGGCGATTC[C/T]TCAGGGATCTAGAAC | 90293 |
rs759098171 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113677 | AAAGGCCTTTTCTGA[A/C]TTCCCACACTAAAGT | 90293 |
rs759103563 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060239 | TGTAAGCAAAACAAA[A/G]GTTACAATAATATCT | 90293 |
rs759107000 | in-del | -/AGC | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107731 | AGGGTTCAAGATCAT[-/AGC]CATTAAGCTCTACTG | 90293 |
rs759110618 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117943344 | TCTTTGTGGCATTCT[C/T]TGTATTTCCTGAATT | 90293 |
rs759116812 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052827 | GCAAGACGCCATCTC[A/T]AGAAAAAAAAAAAAC | 90293 |
rs759118333 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117920706 | TCCCATCTGCAGAAT[C/G]AGAGTATTAGACTGT | 90293 |
rs759126656 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117940009 | TGTTAGTCATCAACT[C/T]TTTGCCGATGCCTGT | 90293 |
rs759133557 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033100 | ACTATGTGAAAAGAC[C/G]AAATCTGCGTCTGAC | 90293 |
rs759136451 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971186 | GGGGCAATAAGGGCT[A/G]CAATTTGGATCTTTT | 90293 |
rs759145007 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117981955 | ACAGTGTAAGATTGT[C/T]TCCTTTAACTTCACA | 90293 |
rs759146771 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002368 | TTGGGAGGCCGAGGT[A/G]GGCGGATCACCTGAG | 90293 |
rs759150299 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902194 | AAATTTCTGTCATTG[C/T]AGAAATCACTAAGAT | 90293 |
rs759172644 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118100973 | ATATCATCTGTTTAA[C/T]GATATTGCAAGATCC | 90293 |
rs759186154 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020454 | AAGATACCATCTCAC[A/G]CCAGTTAGAATGGCG | 90293 |
rs759217133 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002896 | CAAATACTCTTTTTC[C/T]TCCTCATTGTTTGGT | 90293 |
rs759230580 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117996213 | TCATACTTATGAAAA[C/T]ACAAATTTCAAATAC | 90293 |
rs759242527 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044254 | CAAAATGGAAAGATA[C/T]TTCATCTTCATGGAT | 90293 |
rs759249492 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933486 | TGAAATTAGTCTCTC[A/G]CCACACACAAAAACC | 90293 |
rs759258306 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082646 | CTTATGTTGTCTATG[C/T]TTTTGAAGCTTAGCC | 90293 |
rs759264219 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117964842 | AACATGCAGTGTTTG[A/G]TTTTTGGTCCTTGTG | 90293 |
rs759269861 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118020914 | CCAAACACCGCATAT[C/T]CTCACTCATAGGTGG | 90293 |
rs759270109 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959633 | AAAAGTGATCAAGCA[-/T]TAATATCACATTCTC | 90293 |
rs759272799 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912165 | CACTTCCCAAGACAA[A/G]TAAGAATTATCTCGT | 90293 |
rs759285005 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118062809 | ACAGGGTTGAAAGCC[A/G]CATATGGTGACTTAC | 90293 |
rs759289383 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011714 | TGTCATCAAACAATA[C/T]CAAGAATATAGATGA | 90293 |
rs759299549 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117995285 | ACAATTGTAAAAATA[C/T]ATACTTAACTCCTGT | 90293 |
rs759302563 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118003809 | GTACAGAAAATGTTC[C/T]TTCCCTTCCCCTTCC | 90293 |
rs759307751 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118077610 | TCAGCAGCCATGTAA[C/T]ACAAATGTGCACAAA | 90293 |
rs759322498 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117949937 | AAAAGCAACATCTTG[A/C]TACTGCTATGAATAA | 90293 |
rs759335225 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094591 | GACACATAATTGTCA[C/G]ATTCACCAAAGTTGA | 90293 |
rs759335592 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118052121 | ACTTCTCAAAAAACA[C/T]TTTAGGGGAAACTGG | 90293 |
rs759338189 | snp | A/T | 0.124597 | 0.216273 | intron-variant | KLHL13 | GRCh38.p7 | X:118036466 | TATCTGATCTTTGAC[A/T]AACCGGAGAAAAACA | 90293 |
rs759348981 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906938 | CAGTTTATGAAATAA[A/G]ATTAAAATGGACCTA | 90293 |
rs759358879 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117965152 | GTTCTAGATCCCTGA[A/G]GAATGGCCACACTGA | 90293 |
rs759361838 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014659 | TATCACAGAACCTGA[C/T]GATATGTGACTTCGC | 90293 |
rs759367273 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926410 | CTCGAAAAACAGTCA[C/T]CCTCAAGGATTCCAG | 90293 |
rs759369463 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053538 | GAGATATACCTAATG[-/T]TAAATGAAGAGTTAA | 90293 |
rs759400203 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118049181 | TAAACTGATGCTATA[C/T]AAAAGAAATTTTAGG | 90293 |
rs759406034 | snp | A/G | 0.000674422 | 0.0183509 | intron-variant | KLHL13 | GRCh38.p7 | X:117983453 | AAAAAAAAAAAGGTG[A/G]GGAAAAATGTAGACC | 90293 |
rs759416968 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118087056 | AAAGGATTTCTCTTA[C/T]TGAAAATGAGAAAAA | 90293 |
rs759430697 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999936 | GACAAGAATTGTGCA[-/G]CTGTGTTGTTTTGAT | 90293 |
rs759447859 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015294 | CATCGAGGTGTTAAC[A/G]GAGGCTATCTTATGT | 90293 |
rs759454171 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031662 | ATATATTTAGTTATA[C/T]ATAATATATATAACT | 90293 |
rs759468656 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069557 | TATACAAATAAAAAA[-/C]AATATTAATTCTTCC | 90293 |
rs759493669 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113084 | ATTTTTAATAAAGTT[A/G]GTGACAACTTACCTT | 90293 |
rs759519805 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118104556 | TCAACTTGAATTGAG[A/C]ATTCAAAATTAGATC | 90293 |
rs759524600 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118059720 | AAGGCGTGCTTCAGG[A/T]TCTTGGTCCTACCAA | 90293 |
rs759531717 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118001528 | CATGAGTATACAAGG[A/C]TAAATCCTGATTGTC | 90293 |
rs759539762 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023303 | TGTGATGCTGAATTG[C/T]TGTTTCAGAGAGATA | 90293 |
rs759552094 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118086360 | TGTTTTTCTTAGAGG[C/T]TGTACTAATTTACAT | 90293 |
rs759566721 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118075769 | CCAAGTTATCTACTA[A/G]ACACAAAAGAATTAA | 90293 |
rs759589602 | snp | A/G | 2.3193e-05 | 0.00340528 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117898968 | TTCTTCTGGTGGAAA[A/G]ACTGTGAGTGTGCAA | 90293 |
rs759595007 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080589 | CAGTGAGAATGGCTG[C/T]TATTAAAAAGTAAAA | 90293 |
rs759610577 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073142 | GTCCTCATTCCCTCT[A/G]TTTCTCCCTTCTCCC | 90293 |
rs759611396 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969589 | TCACCAAGCACTCTA[C/T]TTCTATCAAGACAAT | 90293 |
rs759613397 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117993452 | CTTACCAAAGCCTTA[C/T]AATGCAGTTACTATT | 90293 |
rs759613679 | snp | A/T | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118104997 | TGATTAGCTGTCAGT[A/T]AAAAGATTGTCAATT | 90293 |
rs759618968 | snp | C/T | | | utr-variant-5-prime, intron-variant | KLHL13 | GRCh38.p7 | X:117985315 | CCCTCTCTCATCAAA[C/T]TCTCTGGAGTTTTAA | 90293 |
rs759623865 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118024550 | AATAATCAAAATAAA[A/G]TAATAACCCATTTTT | 90293 |
rs759624828 | snp | C/G | 6.9002e-05 | 0.00587335 | missense | KLHL13 | GRCh38.p7 | X:117909961 | CAAGACGCTCAAAAG[C/G]GAGTTTCAAGAACTC | 90293 |
rs759641210 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118091928 | CATTATATACATATC[A/C]GAATATTCTAAGTGA | 90293 |
rs759647449 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019125 | ATTATTAACTATTGT[C/T]CTCATGCCATAGATT | 90293 |
rs759649837 | in-del | -/A | 0.0256233 | 0.11025 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118421 | CCTGGCACACAGGTT[-/A]AAAAAAAAAATAAGT | 90293 |
rs759664457 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117970489 | TAAACCTATGTTTGC[A/C]AGCCAAACAATTGTG | 90293 |
rs759683068 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942291 | ATGTGGTGCTGAGAA[A/G]AATGTATATTCTGTT | 90293 |
rs759685716 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018579 | TCCTAAATTTATGTA[C/G]AATGTATAGGACAAT | 90293 |
rs759699712 | snp | C/T | 0.0230396 | 0.104828 | intron-variant | KLHL13 | GRCh38.p7 | X:118097738 | AAACAGAGATATAGA[C/T]CAATGGAACAGAACA | 90293 |
rs759701299 | in-del | -/AAAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118002599 | CTCTGTCTCGAAAAT[-/AAAT]AAATAAATAAATAAA | 90293 |
rs759701668 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117908434 | GTGTGTGATGTTCCC[C/T]TCCCTGTGACAGACT | 90293 |
rs759706382 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962332 | TTTTTTTTCATTGAG[C/T]ATTTGCATGCAATTA | 90293 |
rs759706594 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117963300 | AACACAATATAATTT[C/T]ATTTTAAACTAAGAT | 90293 |
rs759739061 | snp | G/T | 0.0152462 | 0.0859689 | intron-variant | KLHL13 | GRCh38.p7 | X:118012700 | GGGCAGGGGGCGGGG[G/T]TATTCTGTCTACTGC | 90293 |
rs759743873 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118033519 | AAGGAGAAATAAAAT[A/C]CTTTACAGACAAGCA | 90293 |
rs759744171 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107372 | CAGTCTACTCACCAT[C/T]TACGAGATGCACATT | 90293 |
rs759744800 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117961086 | ATATGCTTGCAAAAT[C/T]GATGTAATCAAAACA | 90293 |
rs759775349 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012202 | ACAGCTCCTGGTATA[C/T]ATTAGGAAGCCTTTG | 90293 |
rs759785367 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117932705 | ATGTCTCTCCAACAT[A/G]CTGATTTCCTTTGGA | 90293 |
rs759788738 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118098196 | TGGACAAAGGGCTAA[C/T]ATCCAGAATCTACAA | 90293 |
rs759817147 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056934 | TTATCAGCCTCCGAG[A/C]ACTTAAATCTATCTA | 90293 |
rs759825824 | in-del | -/A | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118109830 | GCAAGAAAACTGCAG[-/A]AAAAAATCCTTTGAG | 90293 |
rs759829165 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033811 | AAATTGGATAAAGAG[C/T]CAAGACCCATCACTG | 90293 |
rs759834894 | snp | A/G | 0.00105904 | 0.0229869 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897533 | TAAACTCGGAATTGT[A/G]ACTGCTCTTCTGGTT | 90293 |
rs759859378 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118065746 | GGCTCCATTAGGCTA[C/G]AGCAAGCTCCAGTGT | 90293 |
rs759870294 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118101845 | TCTCCTGCCACCTTG[C/T]GAAGAAGGTGCTTGC | 90293 |
rs759888170 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898695 | AAACATCAGCTTCTA[C/T]GGGATACATTTCCAG | 90293 |
rs759901543 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118004772 | GGAGAGGCCTGACAG[A/G]TACCACCTTAATCAA | 90293 |
rs759909900 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117923945 | CATTTTTAACAAATT[C/T]GGAGTGTCTTTTATT | 90293 |
rs759915938 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955269 | GAATTTCCCAGTTCT[A/G]TTCAACTTCACAAAG | 90293 |
rs759937275 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025242 | AGTAGTCCCTGCTTA[C/T]GCATGGTTTCACTTT | 90293 |
rs759967453 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101866 | GGTGCTTGCTTCCCC[-/A]TTCACCTTCCACCAT | 90293 |
rs759970770 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921347 | GATGTGATTAAAATA[-/T]CATGTTTTACATGAC | 90293 |
rs760012493 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118046223 | ACAAAAAGAATGTGA[G/T]CTTGTCAATTGCAAC | 90293 |
rs760035096 | in-del | -/AC/ACAC/ACACAC | 0.112927 | 0.210284 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975177 | GAAGGAGAAATACAT[-/AC/ACAC/ACACAC]ACACACACACACACA | 90293 |
rs760043725 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117946097 | TGATTCCCACTCCAA[A/C]CCCCCATTAATAAAA | 90293 |
rs760048089 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118022773 | GCAAATATTTCCTCC[A/C]AATATGTAGGCTGCC | 90293 |
rs760059991 | snp | C/T | 2.58548e-05 | 0.00359538 | intron-variant | KLHL13 | GRCh38.p7 | X:117945593 | GAAAGTTTTTTTACA[C/T]AAGAAAGAAGGGGAA | 90293 |
rs760064541 | in-del | -/A | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118038955 | TGCAACTTGCATACT[-/A]GCTTACCTACAGTAG | 90293 |
rs760064820 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078232 | AATGCAAATCACATG[G/T]GTTTAATTTTAAAAT | 90293 |
rs760071749 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903136 | ATGGTGACAGGCAAA[-/AC]ACACACACACACACA | 90293 |
rs760080996 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117989286 | AATATTCCCATTTTA[A/C]TCATGAAGAAACAGA | 90293 |
rs760083850 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118067827 | CCGAAGGACCTGCCT[A/G]AAGCTGTTTACAGTT | 90293 |
rs760096324 | snp | A/G | 5.14628e-05 | 0.00507235 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117910094 | ACAGTTGTCTAAAGT[A/G]ACCTATTAAGCCAAT | 90293 |
rs760097986 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117966403 | CACTGCTCAAGGAAA[C/T]AAAAGAGGATACAAA | 90293 |
rs760101674 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998168 | AGACAAATACATAGG[C/T]ACACAGAAACCCCAT | 90293 |
rs760111831 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060112 | GACATAACAGAGCAT[A/T]TAAATGCTATGAATG | 90293 |
rs760125750 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117906527 | AGAAAGAACTCAAAG[C/G]GGGTGGAGTGGATCA | 90293 |
rs760127602 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926776 | CACCTCACCCCACCC[A/C]CTATCTTATATTTCC | 90293 |
rs760131832 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117987766 | ACACTTAAAAATATT[C/T]TCTCAATGACTTAAA | 90293 |
rs760139068 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905491 | AAACCAGGTGAGCAC[A/G]TGTGCTAGTGCGTGC | 90293 |
rs760154746 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118070912 | CCCTCCCCCCTTCCC[C/T]CACCCCACAACAGTC | 90293 |
rs760155990 | snp | A/G | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118539 | ACAGAAATGCCAGTA[A/G]AAATGGGATAATCCA | 90293 |
rs760161249 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959774 | TTATCTCATTGATCA[A/G]TGAAAAGCTCTATAT | 90293 |
rs760182769 | snp | A/G | 0.000160929 | 0.00896875 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972764 | GGAGTTGACCTGGAT[A/G]TTTTAAGCACAGGAA | 90293 |
rs760184274 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927320 | AATTTCAAGGCATTG[A/G]TAGCAAGAGGAGTGA | 90293 |
rs760211691 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118079953 | GACCAATGGAACAGA[A/G]CAGAAAACTCAGAAA | 90293 |
rs760216366 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951242 | TATAAAATAAGCCTG[A/G]CATTTTTGTTGAAAA | 90293 |
rs760216862 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938594 | AATATCTCTCACTGC[A/T]CTACAGTGGCAATCA | 90293 |
rs760219566 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938915 | AATAGCCGAAGACTC[A/G]TTTTCATATATTAGA | 90293 |
rs760223897 | in-del | -/AG | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117853 | TCTACTTATAATTCC[-/AG]ACTCCTCCTTGGGAA | 90293 |
rs760230350 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118032480 | CCCCCAGCAGGGGCA[C/G]CCTGACACCTCACAG | 90293 |
rs760235766 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008220 | GTAACTGTGTTTGCT[A/G]GGAAGATGAAAAGGG | 90293 |
rs760259690 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118115474 | CATGAAATCTACTGT[C/T]AAGAAACTGTGGCTT | 90293 |
rs760265771 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968271 | GTCCATGAATGGAGG[A/G]TGCAGCCTTGGTGAG | 90293 |
rs760268511 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089543 | TAAGACAGAAAGTTT[A/C]ATTCATAGGGCAAGA | 90293 |
rs760278089 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118110795 | TGAATTTCTTACCCC[C/T]ACCCCCACAAAAGAC | 90293 |
rs760284388 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117920653 | ATTATCAGCTTTTAC[A/C]TTATTTTGAAAAATA | 90293 |
rs760298567 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118062306 | ATTTGTCATGACATG[-/T]TTTTCTCGGCTTCAA | 90293 |
rs760307705 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107616 | ATTTAATCCTTAAAC[G/T]AGATGAGATAGTTTA | 90293 |
rs760332020 | in-del | -/T | 2.28185e-05 | 0.00337768 | frameshift-variant | KLHL13 | GRCh38.p7 | X:117919569 | AACTGGCAGAATCTG[-/T]AGGAAACTGGCAGCT | 90293 |
rs760355546 | snp | A/G | 4.79939e-05 | 0.00489843 | intron-variant | KLHL13 | GRCh38.p7 | X:117901810 | CTTATATATTATATT[A/G]TGTTCACATGATACT | 90293 |
rs760358450 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089980 | CAGCTACTCAAGAGG[C/T]TGAGGCAGAAGAATC | 90293 |
rs760361246 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117910239 | TTCTTATCTAAATGT[A/G]TCAATGATCTACAAA | 90293 |
rs760375309 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118075137 | ACATATATGGGTTAA[C/G]TAGGCAAAGTGGGGA | 90293 |
rs760380216 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052383 | AAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCGCC | 90293 |
rs760383040 | in-del | -/TTA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007018 | CGCTCCCTAGAGGCC[-/TTA]TTAGACTTAGCACTG | 90293 |
rs760386711 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118009883 | TCTTCCTACCCATGA[A/G]CATGGAATGTTCTTC | 90293 |
rs760394656 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081122 | CTAGAGGGGTGAGGG[A/G]CAGAGTGGGGCATGG | 90293 |
rs760403659 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118002785 | GGCTATGGTGCTCCC[C/T]CACATGTATTTCAAA | 90293 |
rs760412841 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002246 | TTTGGTCAGGAGAGA[A/T]GATTTAAAAATTGTT | 90293 |
rs760413691 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971464 | ACAGTTTTTGAAAAA[C/G]AAATATAGCTGGTTT | 90293 |
rs760416160 | snp | A/T | 0.111166 | 0.207907 | intron-variant | KLHL13 | GRCh38.p7 | X:118020436 | GCAAATCAAAACCAC[A/T]GTAAGATACCATCTC | 90293 |
rs760417001 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074275 | CCCTTGTAGGTTGAG[-/A]AAAAAACTGGTTCTC | 90293 |
rs760419112 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117920545 | ATATGTGACAATGCA[C/T]GTTTTCTTTCACTGT | 90293 |
rs760444536 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117943798 | GCTCGGAGGAGTTTG[C/G]TGTTACCTACCTTCT | 90293 |
rs760446283 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118082261 | TTTTCTCCACATCAT[C/T]CCCAGCATTTATTTC | 90293 |
rs760451791 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942920 | AGTTTCTTCATAGTG[C/T]CAATGATCTTTACAA | 90293 |
rs760459980 | snp | A/C | 0.016289 | 0.0887646 | intron-variant | KLHL13 | GRCh38.p7 | X:118019955 | TTGTTCTTTTGGCTT[A/C]GGATTGACTTGGTGA | 90293 |
rs760463300 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118067651 | ACTTTTTAAACTTTT[C/T]TTTAACTAAGACACA | 90293 |
rs760466165 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018879 | AGCACTAAGGGGTTG[C/T]TTTTAAGACTTAGCT | 90293 |
rs760475898 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118100087 | TCCCCTCACGCTTTT[A/C]ATTTTTAGATGATGC | 90293 |
rs760485267 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073979 | CTGGGGTCCTCATAG[A/C]TAACTAATTTGTAGC | 90293 |
rs760491785 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922089 | TGTTATTTAGAAAAG[C/T]AGAAGTAAAATAATA | 90293 |
rs760516346 | in-del | -/ACCTT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117960651 | CAGAGACATGCAAAG[-/ACCTT]CTGGTTGTTAACTAT | 90293 |
rs760520411 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111931 | AAAGAGAAAAGAAAA[A/G]GTGGGCCTAGCTAAT | 90293 |
rs760527532 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118001000 | GTAAATTTAATTTCA[C/T]TAAATTAAGGACAAA | 90293 |
rs760539472 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902054 | ACACTTGAAACATAT[C/G]TATTATAGCTATGAT | 90293 |
rs760544359 | snp | A/C | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117964100 | TAATGCTAGATGACA[A/C]GTTAGTGGGTGCAGC | 90293 |
rs760566109 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117949750 | ATAGCAGTTCATGTT[A/T]TACAGAAACCCAGGT | 90293 |
rs760587137 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044149 | ATAATAGCCACACAT[A/G]AAGGAAAATACCTAA | 90293 |
rs760593698 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118097109 | gaaggaaataaaggg[C/T]attcaattaggaaaa | 90293 |
rs760614494 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948125 | GGATGCTGCTAAACA[A/T]CCTACAAAACAGGAC | 90293 |
rs760630560 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030219 | CTTATAATTCTGTTA[A/T]TACAAGTAAAGAAAC | 90293 |
rs760641602 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041522 | TGACAGAGTGAGACC[C/T]TATCTCAAAAAGAAA | 90293 |
rs760667230 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117924986 | AATGTATCAAAACTT[C/T]AACCTCTATTAAATA | 90293 |
rs760681099 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117964193 | AACTTAGAGTATAAT[-/A]AAAAAAAAAAAATTG | 90293 |
rs760683016 | in-del | -/TCT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118068780 | AGTAGTCACAGCACA[-/TCT]TCTTCCCTGAGACTA | 90293 |
rs760717464 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118086226 | CAGGCGTGAGCCACC[A/G]TGCCCGGATGTCTTT | 90293 |
rs760720900 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118048471 | AGCTTCACCTGTATC[-/T]TTTTTTTGTTGAGGA | 90293 |
rs760721312 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118058589 | CCCAAATGAATGCTG[A/G]TCATGAATTTATCAC | 90293 |
rs760731027 | snp | A/C | 4.56387e-05 | 0.00477674 | missense | KLHL13 | GRCh38.p7 | X:117919564 | TCCAAAACTGGCAGA[A/C]TCTGTAGGAAACTGG | 90293 |
rs760750024 | snp | A/G | 0.000158428 | 0.00889883 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028505 | ATAATGACCTGTTCA[A/G]GAGGAAAAGAAGCCA | 90293 |
rs760759866 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118012213 | TATATATTAGGAAGC[C/T]TTTGTGCCAGACTCT | 90293 |
rs760763065 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118103506 | AATGACATTTCAAGA[C/T]CATTCTGAAAGAAAA | 90293 |
rs760763745 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056706 | TTCATTATCAAGGCA[C/G]CATGGTAATAGGCCT | 90293 |
rs760776858 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118097080 | GAAGTTCTGGCCAGG[A/G]CAATCAGGCAGGAGA | 90293 |
rs760808192 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959321 | CTAAGGGGTTATCTA[C/T]TGGACAATGATTCAC | 90293 |
rs760808593 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118079294 | GAAGTCTAGCCAGAG[C/T]AATCATGAAACAGAA | 90293 |
rs760809348 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969462 | TTTATATGGTTTGCA[C/T]CTGTCAGGGGCAGAG | 90293 |
rs760811124 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117939895 | ATTCTGTAGGATTCC[C/T]GTACACTCTGATGAT | 90293 |
rs760812988 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118048956 | AATTTTATTCATAAG[A/T]ATTTAAGTAATTCAC | 90293 |
rs760813473 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915692 | ATATTTAAATTGTAA[A/T]CTTTTGAGTTCAATT | 90293 |
rs760816820 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007401 | AAAAAAAAGAGAGAG[A/G]GACCTGCCAGCCCTG | 90293 |
rs760823893 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118040723 | GGTTACAGAACATCA[A/G]GTAGATTTAGCTCAA | 90293 |
rs760839794 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933089 | TTTTTTTGCTGTTGA[A/G]TTCCTTATACATTTT | 90293 |
rs760850970 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117916505 | TAGAAGGGAGGTTGG[C/G]TCTTGTTCCATTAAC | 90293 |
rs760855918 | in-del | -/CGCT | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118018207 | TTCTACACTGACCTC[-/CGCT]CACTCTTAACTCTTT | 90293 |
rs760858407 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:117908396 | TATCCCTCCCCTAGC[C/T]CCCCAACCCCAGACA | 90293 |
rs760863291 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999138 | GATAAAAACAAAAGG[C/T]TCCTCAGGGATCTAG | 90293 |
rs760864069 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940488 | TGGGAAGAAAGTCAA[C/T]GGTAGCTTGATGGGG | 90293 |
rs760864774 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118091023 | CTCAGCAAACTATCG[C/T]AAGGACAAAAAACCA | 90293 |
rs760870908 | in-del | -/TAA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991694 | GTTATTCTTAAAAAG[-/TAA]TAATAATAAACAACT | 90293 |
rs760873653 | in-del | -/AAAAAAAAAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007371 | GAAGGAGACCCTGTC[-/AAAAAAAAAAA]AAAAAAAAAAAAGAG | 90293 |
rs760874570 | snp | G/T | 0.000114235 | 0.00755674 | missense | KLHL13 | GRCh38.p7 | X:117909547 | TTGGGGCATCCATGG[G/T]GGCTAACGATTTCCA | 90293 |
rs760907811 | snp | C/T | 4.58127e-05 | 0.00478584 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899316 | TCTGACAGTGGTCAT[C/T]GGCGCCTTCTGGATC | 90293 |
rs760918276 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999776 | ACAGAGCAGGCAACA[C/T]ATGGTGAATCTGAAG | 90293 |
rs760924118 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982295 | GATGTTATTAAAATA[A/T]CAAAACTCACTTATT | 90293 |
rs760934174 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943111 | GCTGGATATGAAATT[A/C]TGGGTTGAAAATTCT | 90293 |
rs760944123 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018460 | ATTTAGTAAATTAAT[C/G]AGCAATTACTACATA | 90293 |
rs760947763 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907762 | CAACAATCTAGAAAA[C/T]CTGGTCTTAGAAAAA | 90293 |
rs760952816 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117921993 | AATCTTTCACAAATG[C/T]CCCTTTTTCTTTGTA | 90293 |
rs760975661 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117917120 | AGGGTAAAGGAAAAC[C/T]TGGGTTTTGCATGTT | 90293 |
rs760978189 | snp | A/C | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973392 | TAAACCTCAGCATAG[A/C]CTTAGGCTACCGCTA | 90293 |
rs760996092 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117925058 | GAAACATCTAATGAG[C/T]TTGATAAATTTTAAA | 90293 |
rs761009032 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072672 | AAAAGTGGGCGAAGG[A/G]CATGAACAGATTTGT | 90293 |
rs761009348 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948962 | TTTAAAGACAAAAGG[-/A]AAAAAAGCCTAAGCC | 90293 |
rs761009425 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117993280 | TTAAACTAAGGCAGT[A/G]GTAGTGGGTGACATT | 90293 |
rs761029843 | in-del | -/TAG | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012108 | AAGCAGCCAGAGTTC[-/TAG]TAGTACCTTTTACTG | 90293 |
rs761033836 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117932520 | TTACAGGATTTCATT[C/T]TACTTTATTCCTTAA | 90293 |
rs761033983 | in-del | -/ATA | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118083509 | CATATGATTCCACTC[-/ATA]ATGAGGAATTTTTTA | 90293 |
rs761039369 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117980913 | TAAAGATGTCCTTAT[A/G]GTAATGTTATTTGCC | 90293 |
rs761060660 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014796 | GGGGCTGATTCCCCC[-/A]ATACCCCCAAAATGG | 90293 |
rs761075860 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912494 | TCAAATTTATCCAGT[A/G]AGAAAACGATTGCTA | 90293 |
rs761078898 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907214 | CTAGTTCCTAGATGG[A/G]TATACCATAGGAGCA | 90293 |
rs761088471 | snp | C/T | 2.38393e-05 | 0.0034524 | synonymous-codon, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117945563 | GTGTTGGTCTTCCTC[C/T]TCCACGAGAGATCTG | 90293 |
rs761090209 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055240 | TTCATAGCCACAGTA[A/G]AAACCATCTTATGGA | 90293 |
rs761097739 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924093 | AAATGAATGACCCCA[C/G]TATCCAATTCCATAT | 90293 |
rs761099004 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064779 | AGCCTCACTACATAT[C/T]TGCTAGCTGTTTTCT | 90293 |
rs761099700 | in-del | -/GT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085798 | GTAATATTCCATGGT[-/GT]GTGTGTGTGTGTGTG | 90293 |
rs761122713 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004665 | ATATTGAAAGTCTGA[A/T]AAGGGATAAGATATT | 90293 |
rs761130095 | snp | A/G | 0.00149212 | 0.0272733 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973433 | GTGACTAAATTCAGC[A/G]GCCTGCTTTCCTCCT | 90293 |
rs761159036 | in-del | -/G | 0.000645578 | 0.0179547 | intron-variant | KLHL13 | GRCh38.p7 | X:118053845 | AGAGAGAGAGAGAGA[-/G]AGAGGAGAGAGAGAG | 90293 |
rs761177337 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942179 | AGTTCTAATTTGATT[C/G]CACTGTGGTTTCAGA | 90293 |
rs761188789 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065578 | ATATGCACAGAGAAA[C/T]CAGAGAAAGCCAGTC | 90293 |
rs761210049 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118084117 | TTGAGGCCAGGAGTT[C/T]GAGATCAGCCTGAGC | 90293 |
rs761214150 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897952 | CAGAATACATATAAT[A/C]TGCAAGTTACCTCAA | 90293 |
rs761215546 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076832 | CAGTTCCTTAAAATC[-/T]TTTTTCTCTTTCTTT | 90293 |
rs761218835 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069731 | AATTAAAAAGTGTAC[A/T]AAGTAAAAAGTTACA | 90293 |
rs761221064 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975149 | CAGCAGGGGCAACTT[A/G]TTTGAAATCCAAAGA | 90293 |
rs761232528 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922639 | GTGTTCGTTTGTGGT[A/C]GTTTGTGGTAGTGGT | 90293 |
rs761237120 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118006631 | AAATCAGCTTGAATT[C/T]ATTCAGGGTCCACCT | 90293 |
rs761240337 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014234 | CTGAATTCTTTTCCC[A/C]GCAAGGAATATTAAT | 90293 |
rs761247068 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118045331 | GTGAACCAAGATCGC[A/G]CCACTGCACTCCAGC | 90293 |
rs761247658 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997348 | TGAAAAGTGTTCAAC[C/T]ATCTTTTAAAATGTA | 90293 |
rs761250512 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118079668 | AATGGAAAAACATTC[C/T]ATTCTCATGGATTTG | 90293 |
rs761256361 | in-del | -/GG | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029282 | TTACCTCAGGAACTT[-/GG]GGTCTGAGAAGTCTA | 90293 |
rs761259800 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015728 | TTATAGGAACAAATA[-/T]GGTGATAAATTTCAT | 90293 |
rs761264607 | snp | A/G | 2.49928e-05 | 0.00353494 | intron-variant | KLHL13 | GRCh38.p7 | X:117901782 | TATGGAAAGATAACC[A/G]TATAGTTAAAAGCTT | 90293 |
rs761288178 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938259 | CATATTTCATGCAAC[A/G]ATTCACCTACTGATA | 90293 |
rs761288847 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944725 | CAGTACCATATTGCT[C/G]TCTAATTCAGCAATG | 90293 |
rs761288941 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117954654 | GAATGCACATGTGAT[A/C]ATGGTGGTAGGGAGA | 90293 |
rs761316755 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951592 | CTCTTTAGTTACAGA[A/T]GAGATTTTATAAAAT | 90293 |
rs761321629 | snp | C/T | 2.31436e-05 | 0.00340166 | intron-variant | KLHL13 | GRCh38.p7 | X:117945430 | AAGAGACAGCTTAAA[C/T]TACCTGTAACACCAC | 90293 |
rs761345938 | snp | C/T | 0.108358 | 0.206004 | intron-variant | KLHL13 | GRCh38.p7 | X:118021687 | CTATTGTGAATAGTG[C/T]CGCAATAAACATACG | 90293 |
rs761351514 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117927190 | CAGGCCTGAGCTACC[A/G]CGCCCGGCCACTTCT | 90293 |
rs761356598 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118038024 | GTGAGGTAGCATGTA[C/G]AGAATAAGGAAAAAT | 90293 |
rs761364844 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117966278 | ATAACAGAAAACAGA[A/C]AGCCAAATCATGAGG | 90293 |
rs761381481 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089662 | AAAGAAAGAAAGAAA[-/G]AAAGAAAAAAGAAAG | 90293 |
rs761383839 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954758 | ACAGAGGAAATAGTT[A/T]CAATCCTCTGGTGAA | 90293 |
rs761407081 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950520 | AGTGTCAAAAGTATA[A/C]TATAGATATTTCAAG | 90293 |
rs761414925 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924428 | ATAAATCTTTTCCCC[-/T]ATTTAAGAAGCCTTT | 90293 |
rs761420397 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118095448 | ATAATAATGGGAGAC[G/T]TTAACACCCCACTGT | 90293 |
rs761432659 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904655 | TTATGAAAATTCTAT[A/T]AAATTCAAATTTCAT | 90293 |
rs761435902 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118114172 | TATCAAACATCAATA[A/C]AAATCAAACAATTTG | 90293 |
rs761440163 | snp | A/C | 2.28292e-05 | 0.00337847 | missense | KLHL13 | GRCh38.p7 | X:117899064 | ATATTTCTGCACTAT[A/C]TCTACCATACAACGA | 90293 |
rs761444282 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118038873 | ACCCCAGGCAGCACC[A/G]TTCACAGCTACAGGA | 90293 |
rs761446126 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118032267 | ACCTGCCTGCCTCTG[C/T]AGGCTCCACCTCTGG | 90293 |
rs761463437 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070348 | TTTACATTTCTATTA[C/G]GATTTCTTTCACCCC | 90293 |
rs761473886 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974688 | AAACTACTATTTTCC[C/T]GTGAAGCACAAAACA | 90293 |
rs761478085 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118077906 | TGGCATATATAAAAG[C/T]ACCTTACAAACTCTA | 90293 |
rs761486322 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088562 | GCCTTACAAACTAAG[A/G]AACTGTTGCCTACAT | 90293 |
rs761487786 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959730 | AACCCTGATTAAGAT[A/T]ATTATGCACATTATA | 90293 |
rs761488943 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117988607 | CAATCTAATGGGGAA[G/T]ATGGGGGTCAAAGGA | 90293 |
rs761491367 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905454 | GGAAAGCAGCATTTT[G/T]AAGGAATTATATTTC | 90293 |
rs761517614 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118095917 | CAGAATCTCTGGGAC[A/G]CATTCAAAGCAGTGT | 90293 |
rs761520653 | snp | C/T | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117967 | CTTAAGGAAGTGATG[C/T]GGTGAGTGTGGAATC | 90293 |
rs761523238 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118009593 | TCTGAGGGCTCTGTT[C/G]TGTTCCATTGATCTA | 90293 |
rs761524519 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118105700 | TAGTAGAGTGCTTTA[C/T]GTATAATTGCTTGTT | 90293 |
rs761527481 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118098387 | GAGATACCAACTCAC[A/C]CCAGTTAGAATGGCA | 90293 |
rs761534411 | in-del | -/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118032464 | CCTAACTGGGAGGCA[-/C]CCCCCAGCAGGGGCA | 90293 |
rs761544178 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045787 | ACTCCAGCTTGGGCA[A/G]CAGAGTGAGACTCTG | 90293 |
rs761557386 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117918790 | ACTTACATTCTTACA[A/G]GTTTGCCCATAGGTA | 90293 |
rs761557431 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118061096 | TTCAATCCACAACAG[A/T]CACACTGAAAAAAGA | 90293 |
rs761565317 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968128 | GTCTGAAAACCATGT[A/C]ACATGAGAAGACGCC | 90293 |
rs761590491 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118008932 | TAAAGGTTTTGTACC[C/T]AGTACAAAGTAACGC | 90293 |
rs761595658 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025118 | CCTGTTTTCACCCAA[C/T]ATGGCCACATATTAT | 90293 |
rs761598670 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025844 | CAGCTTGTGCTAGTT[A/C]TGCTGTCACACTCAA | 90293 |
rs761605214 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971417 | CTCACCTCCATTAAC[C/T]TGTCACCTCCATTAA | 90293 |
rs761606715 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023405 | GTCTTTTAAGGGCTC[-/T]TTTTCTATTCTTAAA | 90293 |
rs761607674 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118089416 | GTAAGGAAAAACCAC[C/T]CTCTTAGGTATCAAG | 90293 |
rs761610487 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117919276 | CGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 90293 |
rs761613055 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088830 | GTATATAAAAACATA[A/T]AATGGTTCTGAAAGG | 90293 |
rs761614117 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117979151 | TGGCCAGGCTGGTCT[G/T]GAACTCCTGGCCTCA | 90293 |
rs761620745 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001503 | TAAAGAACTAATGCA[A/T]TTGAATGAACATGAG | 90293 |
rs761621431 | snp | A/G | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:118019814 | TTGTAGATATGAGGC[A/G]TTATTTCTGAGGGCT | 90293 |
rs761627166 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040085 | AGTGACCAAAGACTT[A/G]GATCACAACACCCAT | 90293 |
rs761637420 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117970626 | GGAATATAGAGAAGT[A/G]CTGATGAGAAAAACA | 90293 |
rs761648800 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111870 | GCACTCCAGCCTGAA[C/T]GATAGAGTGAGAGAG | 90293 |
rs761658341 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900672 | GATTAAAAATTTCAT[A/C]AGGCAGTGGTCAATC | 90293 |
rs761666667 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118035175 | GGTACAAGGAGGAAC[C/T]GGTACCATTCCTTCT | 90293 |
rs761667166 | snp | A/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:117980118 | ATATAGAAGCAAGAC[A/T]GCCAAAGTGGCATGA | 90293 |
rs761671135 | snp | A/C | 0.000103484 | 0.00719243 | missense | KLHL13 | GRCh38.p7 | X:117910096 | AGTTGTCTAAAGTGA[A/C]CTATTAAGCCAATTA | 90293 |
rs761675738 | snp | A/C/T | 0.00211738 | 0.0324783 | intron-variant | KLHL13 | GRCh38.p7 | X:118002219 | ATGTCATTTTCCTCA[A/C/T]GGACTTCATGGTTTG | 90293 |
rs761675883 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117993554 | CTGTAAATATTGGAA[A/C]TGGAATTTGAACCCA | 90293 |
rs761677458 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118051496 | CAGTGAGCCGAGATT[A/G]CACCACTGCACTCCA | 90293 |
rs761682091 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017654 | GTCAGTAGCACCCCA[C/T]ATGTCCTTTCAACAG | 90293 |
rs761687127 | in-del | -/AAAAAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117929779 | AGACATCGTCTCTAC[-/AAAAAAA]AAAAAAAAAAAAAAA | 90293 |
rs761688862 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975179 | AGGAGAAATACATAC[-/AC]ACACACACACACACA | 90293 |
rs761697317 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039112 | GATTAATCATCTGCT[A/G]ATTAAAGGGCCCTTG | 90293 |
rs761715523 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117984806 | AAAATGCATCAAAAT[A/G]TCTTTAAATACAGCT | 90293 |
rs761727292 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902974 | GGTCCACCATATGAT[A/G]TAGTTCTGGGCAGCG | 90293 |
rs761728639 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118058666 | ACAATTTCTTTCATT[A/C]AGGCAGAAAGAATTT | 90293 |
rs761730902 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080895 | ACTGGATAAAGAAAA[C/T]GTGGTACACAGACAG | 90293 |
rs761737362 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942416 | TTAATCTGTCTAATA[C/T]TGTCAGTGGGGTGAC | 90293 |
rs761750146 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924144 | TATGTCTATCTTTAT[A/C]CAAATGATATCTGTC | 90293 |
rs761763142 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118042572 | TGGAAACTGTACAAA[C/T]ACATGAAAATTAAAA | 90293 |
rs761772209 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099451 | TTATAGACTTTCAAA[A/C]GGCTAAGTTAAAGCC | 90293 |
rs761773590 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118066895 | CTCAAAATCATTAGT[C/G]ATTAAGGTACGTGCC | 90293 |
rs761791735 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117918920 | TGCTTGTATAGTCAT[C/T]AAGGTGAATAAAACC | 90293 |
rs761793460 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117929707 | AGCACTTTGGGAGGT[C/T]GAGGCAGGAGGATTG | 90293 |
rs761843201 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049440 | GTGTTCTTTAAAAAA[C/T]AGTTTGTTAGACAAA | 90293 |
rs761845810 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074963 | AACTACTGGTTCAGC[C/T]CCTTTGGATTGGAAA | 90293 |
rs761846248 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913715 | GGACGTGGTGGCACA[C/T]GCCTGTATTCCCAGC | 90293 |
rs761846960 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117920407 | AGTCACTAATCAAGG[C/T]AAAATGAGGTTACAA | 90293 |
rs761864273 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020405 | TGGGCTGAGACAATT[A/T]GGCCATCAGAGAAAT | 90293 |
rs761868036 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117955925 | CCACTCACCTATCTA[C/T]ATATTCACAGTTACC | 90293 |
rs761886515 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118110813 | CCCCACAAAAGACTC[C/T]CTTGTGCTAAAGAAG | 90293 |
rs761899931 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118013623 | ACAAAATGTACATTA[A/G]AGGGAGTAAAGAGAG | 90293 |
rs761902249 | snp | A/C | 2.31449e-05 | 0.00340175 | missense | KLHL13 | GRCh38.p7 | X:117909987 | AACTCCCCTGTGCTC[A/C]GCAATGCAGGAAAAT | 90293 |
rs761919238 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056987 | TATTTATTCCCCTGT[A/C]AAAACCACACTGTAC | 90293 |
rs761934926 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117934849 | TTTTTTTTCTTCCAG[A/G]ATCACATACAAATGG | 90293 |
rs761937223 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118057695 | GTCGGGTGTGGTGGC[A/G]GACACCTGTAGTCCC | 90293 |
rs761940484 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031481 | TTTAGATATATATAT[A/C]GATATATATATTTAG | 90293 |
rs761963453 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117978022 | CTAGATACTCAGATA[C/T]GTAGTCTTGCCACAA | 90293 |
rs761969084 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118071077 | CATGTCCCTACAAAG[G/T]ACATGAACTCATCAT | 90293 |
rs761983512 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117916368 | CATATCTATCCTTCA[C/T]TGTCATCCTTCTGTA | 90293 |
rs761986766 | snp | A/G | 2.54741e-05 | 0.00356881 | intron-variant | KLHL13 | GRCh38.p7 | X:117901966 | TAAAAAAAAAAAGAA[A/G]AGAAAATTATTTTTA | 90293 |
rs761997334 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030663 | GGATTAATGCCATTA[C/T]CATGGGAATGCGTTC | 90293 |
rs762005987 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018653 | GAACCATGGTATGTA[C/T]AACTGTCCATTTTTA | 90293 |
rs762011732 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999065 | ACCCTCTACTGACAA[A/T]ACTTCAGTGTCAGGT | 90293 |
rs762014730 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979864 | AATAGTGATCACTCA[C/T]CTGTTTAGTCATCTC | 90293 |
rs762021320 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023037 | ACTTTGGTATGTAAT[-/C]CATTTTGCGTTTATT | 90293 |
rs762045692 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117948026 | TCATTCTCAATGTGG[A/G]GAGGGGGAGCAGGAG | 90293 |
rs762046328 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117976696 | ACTTGGCTTCTATTA[C/T]GTACAATTGCATAAA | 90293 |
rs762066911 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117990864 | GAAATGTCTCAAATC[C/T]CTTTCTCACCCCATT | 90293 |
rs762067535 | snp | C/G | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118078433 | TTTCACCCCCATTCT[C/G]CAGCAAGCACTAACT | 90293 |
rs762075759 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006384 | TGCCAAAAAAAAAAA[A/G]AAAAACCAAACCTCT | 90293 |
rs762079531 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117960337 | GATCAGAACTTTCCT[A/G]GATGCACCTCCAAGT | 90293 |
rs762080513 | snp | A/G | 0.000172117 | 0.00927518 | intron-variant | KLHL13 | GRCh38.p7 | X:117983448 | CTGAAAAAAAAAAAA[A/G]GGTGAGGAAAAATGT | 90293 |
rs762082219 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096545 | AACTATTCCAATCAA[C/T]AGAAAAAGAGGGAAT | 90293 |
rs762089832 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117989642 | AGAGTTCTCTTTCAT[C/G]TAGTAATTAGCAATT | 90293 |
rs762094543 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070517 | GGCCTAGTATATGGT[A/C]AATTTTAATAAATGT | 90293 |
rs762103514 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023688 | ATTCTCATGCCTCAG[-/C]CTCCCAAATAGCTGG | 90293 |
rs762109642 | snp | A/G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118017577 | AGTAGAAGAAACATG[A/G/T]CTTCACTCATAAAGC | 90293 |
rs762110301 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907737 | CAGTTCATGATCATG[C/T]GACATAGTCCAACAA | 90293 |
rs762111362 | in-del | -/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991527 | TTCCATGACTCCTTA[-/TT]TCTATGGATGTATTT | 90293 |
rs762117501 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011987 | AACAAATAGCTAGTT[A/C]CTTCTGATCCTACCT | 90293 |
rs762118076 | snp | A/G | 2.28295e-05 | 0.00337849 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117920362 | TTCAAGTCGAAGCTG[A/G]TCAAAGCCCTACAAC | 90293 |
rs762125114 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118091997 | TCTCACTCATATGCG[A/G]GAGCTAAGCTATGAG | 90293 |
rs762134674 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117941840 | CTATCTCCTTCAGTT[C/G]TACTCTGATCTTAGT | 90293 |
rs762150734 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117930151 | AGAAAAAAGAAAAGA[A/G]GAAAGAAAAAGAAAG | 90293 |
rs762154037 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104163 | AGAGGTCAAGGCTAC[A/G]GTAAGCTGTGATCAT | 90293 |
rs762165043 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118072583 | CACAACCTACTCATC[G/T]GACAAAGGGCTAATA | 90293 |
rs762168669 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118090158 | TGGATTAAAGACTTA[A/C]ATGTTAGACCTAAAA | 90293 |
rs762170692 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118096944 | CAAAATAATAAGAGC[A/T]ATCTATGACAAACCC | 90293 |
rs762192504 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998469 | TGGCTAGTAATAAGT[A/G]AAGAGATTCTAAAAA | 90293 |
rs762202430 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118063038 | GCAAAACTGACTGCC[C/G]GTAGTGCTTTCAGAT | 90293 |
rs762204473 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083805 | TACATAATGTATATA[A/T]GTATCAAAACATCAC | 90293 |
rs762206264 | snp | C/T | 0.0010983 | 0.0234082 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117937 | TTCTTTGGCTGTTTT[C/T]TTCTTCTTCTTCTTC | 90293 |
rs762214974 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118040033 | AGAGCCACAGCGTTA[C/T]GAGGTTTGAGATGCC | 90293 |
rs762224221 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940423 | TTGTCTTGGCTACAC[A/G]GGCTCTTTTTTGGTT | 90293 |
rs762227477 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071308 | AATGGTATTTCTAGT[G/T]CTAGATCCCTGAGGA | 90293 |
rs762253669 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117960924 | AATTTCATGATTTTA[A/T]TCAAAAGGTAGCACT | 90293 |
rs762258627 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118090842 | ACGTATGTTTATAGC[A/G]GCACTATTCACAATA | 90293 |
rs762265281 | in-del | -/GCA | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:118083293 | GCCCTCGTGTTTACT[-/GCA]GCACTATTAACAATA | 90293 |
rs762268922 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117981249 | GTAAAATAATCACAG[C/T]TTGTTTTGGCATTAG | 90293 |
rs762270297 | snp | C/T | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117033 | GACCCTGAAGCTGAA[C/T]GACCGCTAAGTGGCC | 90293 |
rs762274773 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040591 | AGGGCAAATCTAGGA[G/T]TTATTGGCATTAAAG | 90293 |
rs762285495 | snp | C/T | 2.28027e-05 | 0.00337651 | missense | KLHL13 | GRCh38.p7 | X:117909772 | TTCTCATGAAATCCA[C/T]CGTTTGCACGTAATT | 90293 |
rs762293825 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012021 | CCAACTTACTGTTAA[A/T]TATCTTGTAGACAGA | 90293 |
rs762304986 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118032962 | GAAGCCTCAGGAGCC[A/G]ATGCGATCAAATGGA | 90293 |
rs762312455 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953627 | GAGTTTAAGGCCTCA[C/T]CATGAGTCTAGTAAC | 90293 |
rs762317707 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063804 | AAGCTAGATTTACTT[C/T]ATATCAAATTAATTT | 90293 |
rs762346650 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029984 | AAAAATAATAATAAT[A/G]AAAGAAAAGAAAAAG | 90293 |
rs762353390 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076050 | ACAGACCAGTTTCTA[A/G]TTTTATGTTTATTTG | 90293 |
rs762358502 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117931153 | ATAAGACTATAAAAT[G/T]ATATCCTACATTGAC | 90293 |
rs762366526 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051641 | AACACACACACTCAC[A/G]CGCACATACACACAC | 90293 |
rs762381764 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118003825 | TTCCCTTCCCCTTCC[G/T]GAACAGTTCAATCCA | 90293 |
rs762388296 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117920782 | TTGACTGAAGCATCT[C/T]GGTTTTGTTTTGTTT | 90293 |
rs762399686 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099913 | GGAAGGAAAGAAGGA[A/G]GGAAGAAAGGAAGGA | 90293 |
rs762418614 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117965235 | CCTATTTCTCCACAT[C/G]CTCTCCAGCACCTGT | 90293 |
rs762424448 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044302 | CTAAAATGTCCATAC[G/T]ACCCAATGCTATTTA | 90293 |
rs762433607 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082905 | TTAAAATCAGTTGGC[C/T]GTATATATGTGTATT | 90293 |
rs762440941 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944663 | TATTAAGGGTAGTAA[C/G]AGGACCAATATAATT | 90293 |
rs762452918 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118003990 | TGCAAACAAAATGAG[A/G]GTATTCATGCAGGGA | 90293 |
rs762476604 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108652 | TGTATACTATGCTGT[-/A]AATGAAAGCAGCTTT | 90293 |
rs762477166 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023591 | ATTTTTCTTTTTTGA[C/T]GGAGTCTTGCTCTGT | 90293 |
rs762488932 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028508 | ATGACCTGTTCAGGA[A/G]GAAAAGAAGCCAATA | 90293 |
rs762499866 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117973957 | GTAACCTATAGGGAT[C/T]AGCGATTGTCAAGGA | 90293 |
rs762511193 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117921774 | TTCTCATTTTAATTT[C/T]AAAGCTTTTTAAAGA | 90293 |
rs762512251 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118045291 | AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGGTG | 90293 |
rs762541035 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923993 | ACCTTTGGCAAGTTA[C/T]CTGCTTTTGTAAGGT | 90293 |
rs762563344 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118014745 | AGACCAGCTGACACT[C/T]AGGGAAAATAGAAAA | 90293 |
rs762564002 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118095235 | AAAAAGGCAGGGGTT[A/G]CAATCCTAGTCTCTG | 90293 |
rs762564123 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912350 | ACAAAATGATACTAC[C/T]AGTTGCCAGTCACCA | 90293 |
rs762570249 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101132 | TTGTTTGTGCCTTCT[A/G]TAATTCATATATTAA | 90293 |
rs762574213 | in-del | -/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117995427 | AGATAAAAGTAGTGA[-/T]TTTTTTTTTAATTTT | 90293 |
rs762578752 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117989477 | AAACACCTCCCCTCC[-/A]AAAAAAAAAAAAAGT | 90293 |
rs762580576 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113809 | GTATTCTCTGGTAGA[A/C]TATAAGCACTGTGAT | 90293 |
rs762598887 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115134 | AGTTAAGGGAGCTAA[C/T]ATTTTTAGATGTAAA | 90293 |
rs762611645 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118076748 | TCCCCCACCCCCAAA[C/G]AAGAAGACTGCCTTT | 90293 |
rs762613757 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117990072 | ATGCCTAACTACACT[G/T]TTCTGATGATAATTA | 90293 |
rs762628421 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094647 | GCCAGAGAGAAAGGT[C/G]GGGTTACCCACAAAG | 90293 |
rs762629299 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117996303 | AGATGATTCAGACAG[C/T]TTGCTAAATTTGGTC | 90293 |
rs762633864 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015872 | GTTACCCTCTTATTA[-/T]TTTTATTGGCTAGAT | 90293 |
rs762647163 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916924 | ATAACTTAGCTCATG[A/G]AAGAACTTCAAAAAA | 90293 |
rs762654001 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118101650 | GGCTCTGTGTCCCCA[C/T]CCAAATCTCATCTCA | 90293 |
rs762666475 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051649 | CACTCACGCGCACAT[-/AC]ACACACACACACACC | 90293 |
rs762670559 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118113319 | AAAACATTTTTTTTT[A/T]AATTTCCCTGGATAA | 90293 |
rs762671311 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117965638 | ATCCCTGATGAACGT[A/C]AATGCAAAAATCCTC | 90293 |
rs762679434 | snp | G/T | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:118036891 | TGAACTCAAACAAAT[G/T]TACAAGAAAAAAACA | 90293 |
rs762680050 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118105003 | GCTGTCAGTAAAAAG[A/G]TTGTCAATTTGTTTT | 90293 |
rs762683104 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117926448 | TGATAAACATCTTTG[C/T]CTGCAGAAAGAACCG | 90293 |
rs762684566 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118065056 | CTTCAACTGCTGGAT[C/T]GACAAGACGTTCACT | 90293 |
rs762702257 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118032242 | TTGGAGCCCACCACA[A/G]CTCAAGGAGACCTGC | 90293 |
rs762703411 | snp | C/T | | | utr-variant-5-prime, intron-variant | KLHL13 | GRCh38.p7 | X:117985410 | GGTACAACACTTCAG[C/T]TGTAGCTCCCAAAAG | 90293 |
rs762707754 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044131 | AAGAAAGTAATCCCA[A/T]TTATAATAGCCACAC | 90293 |
rs762722301 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015531 | AGATGAGATTGCACA[A/G]GAAGAATGTAAATAT | 90293 |
rs762739989 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927062 | AGGCGCATGCCGCCA[C/T]GCCCGGCTAATTTGT | 90293 |
rs762740161 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118008227 | TGTTTGCTGGGAAGA[C/T]GAAAAGGGGAAAAAA | 90293 |
rs762742454 | in-del | -/AAAACAGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928860 | AAATCAATGAAATAG[-/AAAACAGA]AAAACAGAAAAAGCA | 90293 |
rs762747752 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117904512 | GAAAAATCTAGAGCA[A/G]GTGGCAGCAAACCTC | 90293 |
rs762751254 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117979133 | GATGGGTTTTTACCA[C/G]GTTGGCCAGGCTGGT | 90293 |
rs762754143 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971262 | ATAATTGTAACCTGA[C/T]TTTAGTGAGGTTTTG | 90293 |
rs762770609 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986176 | AGAAGCTTTAGTAAT[A/G]TAAGCCTAGCATTCT | 90293 |
rs762771761 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118097770 | AGCCCTCAGAAATAA[C/T]GCCGCATATCTACAA | 90293 |
rs762773199 | snp | C/T | 2.28094e-05 | 0.00337701 | missense | KLHL13 | GRCh38.p7 | X:117909823 | TCAGTGGAAATCGTA[C/T]GTTCTTCATTAATTT | 90293 |
rs762773376 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118058333 | ACACACACTAATTAA[G/T]TAAAGTATGCCACAC | 90293 |
rs762785116 | snp | C/T | | | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898397 | CAGATATGTCAAAAA[C/T]ACTTTATGAAAAGAG | 90293 |
rs762797618 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958974 | AGATCAGGCTATCTG[A/C]AGGGCTGGATCAGCA | 90293 |
rs762800834 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038074 | TTGTTTGATGTACAC[A/C]CATTTATGTACCATA | 90293 |
rs762802451 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041690 | TGAGTTATAAGATAT[C/T]ATTTGAAAGTCTCAT | 90293 |
rs762810830 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117917231 | ACAGACATATCCTCT[A/G]CAAAAAAGGATGAAG | 90293 |
rs762819761 | snp | C/T | 0.0369084 | 0.130736 | intron-variant | KLHL13 | GRCh38.p7 | X:118000613 | ACAAAGTAAGGACAT[C/T]TTAAAAGGCAACCCC | 90293 |
rs762821984 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088284 | TCTCTAAACAATTTC[G/T]ATGAGAATTATGTGA | 90293 |
rs762826036 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008803 | TTACTGTGTGGCCTT[A/G]GACAATTTACTTAAT | 90293 |
rs762834799 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117937320 | AGCAACATAGAGTGG[C/T]ATCTCTATGGTACCA | 90293 |
rs762847970 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057151 | GTGTTGGCACAAGGA[C/T]AGATCAATGGAATAG | 90293 |
rs762852414 | snp | A/G | 2.28029e-05 | 0.00337653 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899253 | TCTGAAGTGATTGCC[A/G]CCAATGACATAGAGC | 90293 |
rs762855249 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039038 | GATGACATTTCTACA[C/G]ACACCCTGAGCAAAA | 90293 |
rs762855360 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117918701 | CATCGATTGGTAGTT[G/T]TATGTGTCCTATCTT | 90293 |
rs762874777 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089608 | AGAGAGAGAGAGAGA[A/G]AGAGAAAGAAAGAGA | 90293 |
rs762883333 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950471 | AACTCCATCTCAAAA[A/C]AAGGAAAAGAAAAAA | 90293 |
rs762917610 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117995739 | TATTTCACATAAATT[A/G]AATCATATAGTATCT | 90293 |
rs762923816 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935602 | GAAGGTGAAACAGGC[A/G]TATCTGACATGGTGA | 90293 |
rs762935045 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005208 | GGAACCAATGCCCCA[C/T]AGATAACAACAGATG | 90293 |
rs762941949 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117945171 | TTGATTCTGAGGATT[G/T]TTTAACCTCAGGAAT | 90293 |
rs762946859 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001269 | GGAAACTTTTCGTAG[G/T]CTGGGGCAGGACTAT | 90293 |
rs762973247 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975551 | ACCTGCCACCATGCC[G/T]GGCTAATTTTTGTAT | 90293 |
rs762982608 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025713 | AGAAACCTGCACATC[C/G]TGCACATGTATCCCA | 90293 |
rs762983387 | snp | C/T | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118803 | GGATAGAGCACTAGA[C/T]TCAGAGTCAGAAGAC | 90293 |
rs762989393 | in-del | -/TG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081942 | AATAGTATTCCATTG[-/TG]TGTGTGTGTGTGTGT | 90293 |
rs762996121 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074007 | AGCAAAGTAGAGATT[A/C]GAAAAAATGTCTGTC | 90293 |
rs763004465 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117963465 | AAAGACACTATGAAC[C/T]TTAAACATAAATTGC | 90293 |
rs763005957 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118066762 | GATTTACATCCAGAA[A/T]CAATAAAAAAATTAC | 90293 |
rs763009068 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118098355 | GCCATCAGAGAAATG[A/C]AAATCAAAACCACAA | 90293 |
rs763009637 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941508 | AATTACTGCCTCAAT[G/T]TCAGAACTTGTTATT | 90293 |
rs763011214 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117951097 | CTCTTTCTCCACACT[C/T]CCCAAACAAAAGCTG | 90293 |
rs763029518 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118119163 | GAAGAAACCAAACTT[A/C]CCTACACCTTGATCT | 90293 |
rs763030508 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967973 | CTCAGGCCCTTTAAG[A/G]CAAGCAGAGATTCTG | 90293 |
rs763039522 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118042487 | AAACATTCAAAAAAA[C/T]TGAAGTTACATCAAG | 90293 |
rs763051353 | in-del | -/CCAGGGGTTCAACACCAGC | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118109962 | GAGGATCACTTGAGG[-/CCAGGGGTTCAACACCAGC]CTGGGCAACATAGTG | 90293 |
rs763059588 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | KLHL13 | GRCh38.p7 | X:117963977 | TATTCTCACTCATAG[A/G]TGGGAATTGAACAAT | 90293 |
rs763062902 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118110624 | CCTTATCATCCGCCC[A/G]CCTCGGCCTCCTTAA | 90293 |
rs763063952 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065856 | TCCTCCAGGGCTGGA[C/T]ATCGCTATTTTAATA | 90293 |
rs763072815 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118019266 | CAGTATTTTCATGTG[-/T]TTTTTTGGCTGCATA | 90293 |
rs763081526 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118110213 | TGGGTTTTCCTTTGC[A/G]TGTTTTTAATCTTAA | 90293 |
rs763097811 | snp | G/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985605 | TGGTAAACTGAACAG[G/T]AACAAAGTGTTCATC | 90293 |
rs763103585 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017585 | AAACATGACTTCACT[C/G]ATAAAGCCTGTCCTG | 90293 |
rs763124757 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998239 | CCTAAAAGATATTTG[A/G]ATTTTTTCAACTACA | 90293 |
rs763124974 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012757 | TATAAAGTTACCATT[A/T]TTTTTTCCATTCCAC | 90293 |
rs763128966 | snp | C/T | 4.60167e-05 | 0.00479648 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972795 | CTGGGAATTTCCAGA[C/T]AGCAGGAGAGCTCGT | 90293 |
rs763132214 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092566 | GAAGTTATCTAAACC[-/A]AAAGAAAATGATAAA | 90293 |
rs763144358 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898802 | AATATCTGTATCAAT[C/T]ACCAGAGGGTAATCC | 90293 |
rs763145739 | snp | G/T | 0.0655152 | 0.168717 | intron-variant | KLHL13 | GRCh38.p7 | X:118035770 | GGAGAAGGAAATAAA[G/T]GGTATTCAATTAGGA | 90293 |
rs763146170 | in-del | -/AAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107533 | CCACAAATCTATGAA[-/AAT]AATAATAAGTATAGT | 90293 |
rs763158674 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118019647 | CGTTTAAGTCTTTAA[C/T]CCATCTTGAATTGAT | 90293 |
rs763161171 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118022344 | ATTCCATTACTCTTG[C/T]ATATATACCCAGAAG | 90293 |
rs763181663 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028765 | AGTAACTAATGATTA[C/T]CCATGGAAAAGCAAC | 90293 |
rs763181967 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943753 | CAAGGTTCTTAGCTT[C/T]CTTGCATTGGGTTAG | 90293 |
rs763182739 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955832 | GTACTATGCTTCCCA[C/T]AAAGAAACATATCCA | 90293 |
rs763187501 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924856 | TAGCGTCATTTAATG[A/C]TATTTTGATGCTGGA | 90293 |
rs763198507 | in-del | -/AATATAA | 0.0204488 | 0.0990265 | intron-variant | KLHL13 | GRCh38.p7 | X:117984328 | TGTTTGATGAGCTCT[-/AATATAA]AATTTCATTTATTTC | 90293 |
rs763215557 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084683 | ATGTAGGAGACTATT[C/T]AGATAAATTATAAAA | 90293 |
rs763224717 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102418 | TGTGAATGTGATGTG[G/T]GCAAATGCTAAACTA | 90293 |
rs763228348 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008539 | CACCTAATTCTGCTA[C/G]GAAGAGACAGGAGGA | 90293 |
rs763245110 | in-del | -/TAGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902158 | CATGTTACATTAGAC[-/TAGA]TAGTGTAAGAATCTA | 90293 |
rs763263254 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117914222 | TTTAGAAAAAAATGG[A/G]TATCTGCTTTTTTTT | 90293 |
rs763281192 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117938994 | TGTGCAGAACATGCA[C/G]GTTTGTCACATAAGT | 90293 |
rs763284345 | snp | C/G | 0.000587199 | 0.0171247 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975193 | ACACACACACACACA[C/G]ACACACACAGCCACA | 90293 |
rs763304132 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111552 | CACCTGAGGTCAAGA[A/G]TTTGAAACCAGCCTC | 90293 |
rs763330151 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998262 | CAACTACAGATACAA[C/T]GATATCATCTCTGAA | 90293 |
rs763334157 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117958609 | AGCATCTGCTATGTG[C/T]CAGGCACCACACTAG | 90293 |
rs763335857 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118016210 | TGACAGATGAGGACA[C/T]CACTTGACAAATAGT | 90293 |
rs763352853 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938616 | TGGCAATCATTGTTC[A/G]GTTTCTAGTAAATTT | 90293 |
rs763360499 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104977 | TGTACACAAAAACAG[A/G]GCTCTGATTAGCTGT | 90293 |
rs763363415 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078306 | TCACACTTTTTAGGT[C/G]TACAGCTGAGTTTTG | 90293 |
rs763390452 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071256 | GCATGATTTATAGTC[A/C]TTTGGGTATATACCC | 90293 |
rs763401710 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967379 | AAGTTATTAGCACAA[A/G]TACTTGCCTATCCCA | 90293 |
rs763407757 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117976292 | TATTATGCCAAAGTC[A/C]TTAAAAATAATCCCT | 90293 |
rs763415176 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118090005 | AGAATCGCTTGAACC[A/G]GGGAGGCAGAGGTTG | 90293 |
rs763431477 | in-del | -/CAC | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118017982 | CAAACTGGTGACTCT[-/CAC]CACAACGTGTCCTCC | 90293 |
rs763440184 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047429 | TCATAACACACATGA[C/T]AGGCAACAAAGGGCT | 90293 |
rs763442420 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117906720 | GCGTTTGATGGGTAT[G/T]CTGATTTTAAGGGAC | 90293 |
rs763447199 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070970 | GTCCATGTGTTCTCA[A/C]TGTTCAGTTCCCACC | 90293 |
rs763451287 | in-del | -/AAC | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117998923 | TATAAATTTTATATA[-/AAC]AACTATATGAACATA | 90293 |
rs763454196 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004042 | TTCTGGAAGTCAGAG[A/T]CGGGGAGGCAAGGGT | 90293 |
rs763457627 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117977655 | CTCTTCAGATTAATC[C/T]AAAATATCCATGTTA | 90293 |
rs763470811 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118062603 | CATCTTCTAGTACAG[C/T]TGGGCCCTCACAGTC | 90293 |
rs763475546 | in-del | -/TGTTT | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118048196 | TGTACAAGTAGTTAA[-/TGTTT]TGTTTTATTTTGTTT | 90293 |
rs763486146 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118017472 | GAACCTAGAGAAAAA[G/T]GAACTAACCAATTGG | 90293 |
rs763486777 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936764 | GTATACCCATAACTT[C/T]TGATCAGCTCTATTC | 90293 |
rs763495309 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048841 | ATACCTGCCAACGAC[C/T]TAATTGTAGTTTTGC | 90293 |
rs763498335 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117939569 | CAACAGAGTAAACGT[C/G]TTCCTATTTCTCCAC | 90293 |
rs763498958 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076197 | CACTGGTACCTTATT[C/T]AGAAAGAGGAGCATA | 90293 |
rs763502235 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117929294 | AAACAAATCCAGAAT[A/G]TTAGGAGGAGAGCAT | 90293 |
rs763511524 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117990700 | TGTAAATGGTATGCT[A/G]AGCAGTCAAGAGCAA | 90293 |
rs763534926 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117929219 | AAAACTCTAAGATGA[A/G]ATGGTTTCACTGGTG | 90293 |
rs763537755 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118076749 | CCCCCACCCCCAAAC[A/G]AGAAGACTGCCTTTG | 90293 |
rs763547252 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117960745 | AATGTTTTGGGAAGG[C/T]AGAAATGTAGAGTCC | 90293 |
rs763554256 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118094657 | AAGGTCGGGTTACCC[A/T]CAAAGGGAAGCCCAT | 90293 |
rs763559395 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103449 | CTGAGTAGAAACAAC[C/T]CAAGTAGATAATAGG | 90293 |
rs763560857 | snp | A/G | 2.28313e-05 | 0.00337863 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899034 | AACCTTATGCCATTC[A/G]TCTTTATCTGGATCA | 90293 |
rs763576605 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118021606 | AGTATTCCATAGTGT[A/G]TATGTGCCACATTTT | 90293 |
rs763580686 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045294 | CAGGAGAATGGCGTG[A/C]ACCTGGGAGGTGGAG | 90293 |
rs763590445 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118003900 | CATAGAGACTCTTTG[A/T]GGGGCTTGAGAAGAT | 90293 |
rs763612528 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115309 | AGCTTTCTTCACACA[C/G]TAATTGCAGTATGAA | 90293 |
rs763614044 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118010019 | GGCCATCAGAGAAAT[A/G]CAAATCAAAACCACT | 90293 |
rs763623816 | in-del | -/GT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085797 | GAGTAATATTCCATG[-/GT]GTGTGTGTGTGTGTG | 90293 |
rs763626830 | in-del | -/TAAAAAATTAAAAAG | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069711 | AGAGGCAAAAAGTTT[-/TAAAAAATTAAAAAG]TGTACAAAGTAAAAA | 90293 |
rs763639038 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118087186 | AATGGGTCCTGCCAC[C/T]TACACAATGCTTAAT | 90293 |
rs763646432 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933786 | AGGCATACAGAAACA[A/G]CAACTTAGATCCTAG | 90293 |
rs763648905 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101183 | ATTATTTTATTTTAT[C/T]AATACCTCTTACAAA | 90293 |
rs763660202 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118112368 | GGGGAGATGGCCAGG[A/C]ATCAAATAAGCATAA | 90293 |
rs763660889 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951328 | CATTTATAGTATCAT[C/T]ACACAAAGAAATTAT | 90293 |
rs763665683 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015566 | AGCAACACTCAAGAT[A/C]GGTAGGATGACTGAA | 90293 |
rs763666493 | snp | A/T | 0.0121112 | 0.0768695 | intron-variant | KLHL13 | GRCh38.p7 | X:118036903 | AATTTACAAGAAAAA[A/T]ACAAACAACCCCATC | 90293 |
rs763670125 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118069147 | CACACACACACACAC[A/C]CCCTCACCTGAACTG | 90293 |
rs763673797 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032034 | CTGCGCTTTTCCGAC[A/G]GGCTTAAAAAACAGC | 90293 |
rs763684779 | snp | A/C | 2.46415e-05 | 0.00351 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898869 | ATTTATGACACATTG[A/C]AAAGATAGAACTACA | 90293 |
rs763686118 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023671 | CCTCCCAGGTTCAGG[C/T]GATTCTCATGCCTCA | 90293 |
rs763693057 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117925797 | CATTGGTGATAAAAA[A/T]TTTTTTTCACCTGGA | 90293 |
rs763699764 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935635 | ACAGGAGGAAGAGAG[A/T]GAAGGGGGAGGTGCT | 90293 |
rs763706643 | snp | G/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973052 | TGATGATTCAATCAT[G/T]CCAACTCAACAATAG | 90293 |
rs763711800 | snp | C/T | 0.00211696 | 0.0324653 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986653 | TCTTTCTCGCCTTTG[C/T]TCCAGAGGTCCCTCT | 90293 |
rs763714042 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117996411 | TTACATTTTAAAAAT[G/T]CAATTTTTATCCATT | 90293 |
rs763748483 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926545 | CATGAGTGGAAACCT[C/T]ACAAGGCTGGGGTTT | 90293 |
rs763748488 | snp | A/C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118007674 | CGTGCTGTGCTGATA[A/C/T]AGGAAAACATCTTTA | 90293 |
rs763750256 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113335 | AATTTCCCTGGATAA[-/T]TTTTTTAAGCCAATG | 90293 |
rs763754122 | in-del | -/AG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023310 | CTGAATTGTTGTTTC[-/AG]AGAGATAATTTTTTC | 90293 |
rs763765512 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108992 | TTAAATTTTTTTTTG[G/T]TCTTATAGAGACAGG | 90293 |
rs763765652 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117918720 | GTGTCCTATCTTATC[C/T]ATTAAAAAATGGCTA | 90293 |
rs763769552 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118024695 | TGAGGAAGTACTACA[C/G]ACCCACAGAATGGCT | 90293 |
rs763769847 | snp | C/T | 2.28094e-05 | 0.00337701 | missense | KLHL13 | GRCh38.p7 | X:117909825 | AGTGGAAATCGTATG[C/T]TCTTCATTAATTTTG | 90293 |
rs763793993 | in-del | -/GGAGAGC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903173 | AGAGAGAGAGAGAGA[-/GGAGAGC]GAGAGAGAGAGAGAG | 90293 |
rs763801025 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971292 | GTTTTGTTTTGTTTT[C/T]ATAATAAAGTTGCTT | 90293 |
rs763813610 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963144 | ATTACTCCATTGAAC[C/T]ATATTATAAGAAATC | 90293 |
rs763815017 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900592 | AAGACATTCTGTAGT[G/T]GCTCATGAATTTAAC | 90293 |
rs763818669 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044226 | CACTGATGAAAAATT[C/G]AAGTGGACACAACAA | 90293 |
rs763836190 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008261 | AAGACTGAAAAAGGA[A/G]GGAAGTGAACATCTG | 90293 |
rs763839050 | in-del | -/TTCT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117987814 | CTGTCTACACCTTCC[-/TTCT]TTTTTATTGAGTGAA | 90293 |
rs763845778 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118086747 | TGGCTGCCTCCAGAG[A/T]GAGAAGACTTATTTT | 90293 |
rs763868721 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117917294 | GGTAATTCCTAAAAG[G/T]TCATAGGCAAGAAAA | 90293 |
rs763881758 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088513 | AGATATAACAGACAC[A/G]TATGTGGTACATGTT | 90293 |
rs763924241 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117918754 | ACTATTCAGTAGGTG[A/G]TATGTTTCTATGGAA | 90293 |
rs763937848 | snp | A/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118098375 | CAAAACCACAATGAG[A/T]TACCAACTCACACCA | 90293 |
rs763960155 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118119287 | GGGAAGCATTTCAAA[C/T]GCCAGCTAGAGTATC | 90293 |
rs763960742 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962585 | AAGATAATTGCCTCA[A/G]TATTTTCCTTCAACT | 90293 |
rs763962002 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117950495 | GAAAAAAAAGAAAGT[A/C]TCTTGCATTAGTGTC | 90293 |
rs763972601 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897617 | ATAATCTAATTCCCC[A/G]AACACAACCAGCAAT | 90293 |
rs763986972 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118042521 | CTTCTCTGACCACAA[C/T]AGAATATAACTAGAA | 90293 |
rs764000424 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097774 | CTCAGAAATAACGCC[G/T]CATATCTACAACTAT | 90293 |
rs764033969 | snp | C/G | 2.30449e-05 | 0.0033944 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972798 | GGAATTTCCAGATAG[C/G]AGGAGAGCTCGTTTT | 90293 |
rs764041771 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018678 | TTTTTAAAATGTCTT[C/T]TTTCCTGTCTCTGAG | 90293 |
rs764043279 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057169 | ATCAATGGAATAGAA[C/T]TGAGAGTCCAGAAAT | 90293 |
rs764045026 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107832 | TGGGAGGCTGAGGCA[G/T]GAGGATTGCTTGAGC | 90293 |
rs764048058 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118110022 | CTACCAAAAACAAAA[A/G]AAAATACACCAATTG | 90293 |
rs764061574 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005229 | ACAACAGATGACTGT[A/G]TATATAAAATATTAA | 90293 |
rs764064865 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041688 | ATGAGTTATAAGATA[-/T]TTATTTGAAAGTCTC | 90293 |
rs764065007 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117961518 | TTACATGGCAAAGGA[A/G]ACTTTGAAAATGTGA | 90293 |
rs764074983 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118035171 | CAGAGGTACAAGGAG[A/G]AACTGGTACCATTCC | 90293 |
rs764078663 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118051398 | ACAAAAAAATTGGCC[A/G]GGCGTGGTGGCGGGC | 90293 |
rs764085410 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117963510 | CTTTGCTATTGTGAA[C/T]AGTGCCGCAATAAAC | 90293 |
rs764086724 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941540 | GTCTATTCAGGGATT[C/T]GACTTCTTCCTAGTT | 90293 |
rs764089361 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117984383 | TGTTATCAGCATATA[A/G]AAAGTAAGCATTAGC | 90293 |
rs764097564 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118055781 | TGAATAATAATTTAA[C/T]GTAATATTTTTAAAA | 90293 |
rs764120295 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118004980 | AAGTGTCAAGGTCAT[C/G]AAAGTCAAGAGAAGA | 90293 |
rs764121606 | snp | A/G | 2.38937e-05 | 0.00345634 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909368 | GGCACTTAGGTGGAA[A/G]AAGGTGCGCTTTTCA | 90293 |
rs764133416 | snp | C/G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038088 | CACATTTATGTACCA[C/G/T]AGGACACACCAAACA | 90293 |
rs764135504 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019299 | TGTCTTCTTTTGAGA[A/G]GTGTCTGTTCATATC | 90293 |
rs764143847 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942220 | ATTTCTGTTCTTTTA[A/C]ACTTACTGAGGAGTG | 90293 |
rs764144742 | snp | G/T | 2.59262e-05 | 0.00360034 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909314 | ACGCAGTTCACCTGC[G/T]GCATTTCGCCCACCA | 90293 |
rs764150978 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117900739 | GTAATGTAACTGCTG[A/G]CCTGGCACTGGCAGG | 90293 |
rs764166825 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975638 | TCAGGTGATCCACCC[A/G]ACTTGGCCTCCCAAA | 90293 |
rs764179551 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117946368 | AATAGTATTTTCAAG[G/T]GGCATAAGTAAGAAT | 90293 |
rs764180753 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117964848 | CAGTGTTTGGTTTTT[-/G]GTCCTTGTGATAGTT | 90293 |
rs764185287 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942865 | GAATCTGATCCTGTC[A/G]TTATGATGCTAGCTA | 90293 |
rs764191189 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117927961 | ATGTACTAATAAAAA[A/G]TTGACTTTTACTGTA | 90293 |
rs764201248 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998328 | AGATCTTTAATTGGT[G/T]GCAACTGTCTGGGTC | 90293 |
rs764207793 | snp | C/T | 2.28556e-05 | 0.00338042 | missense | KLHL13 | GRCh38.p7 | X:117901923 | TCCATTCATTTGTTC[C/T]TGGATTGTAACATTC | 90293 |
rs764223378 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012833 | GAGAATAAAGTTCCA[G/T]CCTCTAAAGAAGGTA | 90293 |
rs764229102 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047446 | GGCAACAAAGGGCTA[A/G]TAATTTTAACTTACA | 90293 |
rs764230941 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938537 | TTAACAAGCCCTCCT[A/G]ATGATTCTGACATGC | 90293 |
rs764232240 | snp | A/T | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118918 | ATATGCCCCACAGCA[A/T]TGTTTTGGGTTTCAA | 90293 |
rs764237135 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955898 | CAAAAAGTCTTCACT[A/G]TTACTTACAGCCCAC | 90293 |
rs764245428 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030018 | AAAGAAGTTATGTGA[A/C]GATCTAAAATAATTA | 90293 |
rs764250756 | in-del | -/AA | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118066767 | ACATCCAGAATCAAT[-/AA]AAAAATTACAACTCT | 90293 |
rs764254078 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117933833 | TGATAGGTGATATTT[A/G]TAACAGATAAAATGT | 90293 |
rs764267632 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117925711 | ACTTCTTTGATCTGA[A/T]CCCAACCTTATTTTT | 90293 |
rs764290591 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967976 | AGGCCCTTTAAGACA[A/C]GCAGAGATTCTGCTT | 90293 |
rs764314804 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070323 | TTTGTTATTGCTCAG[C/T]TTTAAGTAGTTTACA | 90293 |
rs764317084 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046220 | ACTACAAAAAGAATG[C/T]GATCTTGTCAATTGC | 90293 |
rs764321395 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117914225 | AGAAAAAAATGGGTA[G/T]CTGCTTTTTTTTTTT | 90293 |
rs764324190 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056930 | TTTATTATCAGCCTC[C/T]GAGCACTTAAATCTA | 90293 |
rs764350773 | snp | A/G/T | 5.71653e-05 | 0.00534603 | intron-variant | KLHL13 | GRCh38.p7 | X:117945619 | GGGAAATTAAAACTT[A/G/T]TACAATTTACAATGA | 90293 |
rs764372445 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905844 | TACTTATTGTAAAAC[A/G]TACAATTAAATTATT | 90293 |
rs764381059 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118016302 | TCTACACCATGAAGA[C/T]ATGATTATACATTAC | 90293 |
rs764401383 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975203 | ACACACACACACACA[C/G]CCACACACATGTATG | 90293 |
rs764402517 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089665 | GAAAGAAAGAAAGAA[A/G]GAAAAAAGAAAGTTT | 90293 |
rs764406894 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938702 | ACATTAGGTAGGAGT[A/G]TAGTAGTGAGGTATT | 90293 |
rs764418487 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117945261 | TTAATAAACTTCATT[G/T]TTTAGAGCCATTTTG | 90293 |
rs764433299 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118017480 | AGAAAAATGAACTAA[C/T]CAATTGGTTATTGCA | 90293 |
rs764433922 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996154 | TTCACACCAGAATGT[A/G]TGTCTCTACACATCT | 90293 |
rs764440667 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070650 | TAATAGATTTTTTTT[G/T]GTCTGCTTGTTCTAT | 90293 |
rs764443674 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921024 | TAATTGTCTCCAAAT[A/G]CCTAAAGGTTTAGTG | 90293 |
rs764448600 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117966641 | AGCTGGAGGCATCAC[A/G]CTACCTGACTTCAAA | 90293 |
rs764452559 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:117976321 | CTTTAATCAGAAATA[C/T]AGTTCATGAACAACA | 90293 |
rs764459943 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117940023 | TCTTTGCCGATGCCT[C/G]TGTCCTGAATGGTAT | 90293 |
rs764484731 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096526 | CTGGTACCATTCCTT[A/C]CGAAACTATTCCAAT | 90293 |
rs764490120 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027235 | CACCATAACAATGCT[A/T]CTGCTCATTTCTCAA | 90293 |
rs764491425 | snp | A/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986697 | TTCCAAACTCCACTT[A/T]CCTGAACTCAACCCA | 90293 |
rs764492558 | in-del | -/ATA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081502 | ATTTTTGGGGTGCAC[-/ATA]ATATTTTTGATACAA | 90293 |
rs764492571 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117977898 | CTTATACACTTACAT[A/G]CATGTGTGTTTGTGT | 90293 |
rs764497171 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117906736 | CTGATTTTAAGGGAC[A/G]CAATCATTTTCTACA | 90293 |
rs764497825 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016612 | CAGCCAGTCACTCTC[C/T]GAAAGGGCTCCCTTA | 90293 |
rs764513276 | snp | A/G | 4.56574e-05 | 0.00477772 | missense | KLHL13 | GRCh38.p7 | X:117919636 | AGCTTTGCAGTATAA[A/G]TGAAATCAATAATTT | 90293 |
rs764527771 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089639 | AAGAAAGAAAGAAAG[-/AA]AGAAAGAAAGAAAGA | 90293 |
rs764537482 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007124 | AAGTCAAAAGTAGGA[A/G]TCAGCCAGGTGAGGT | 90293 |
rs764538281 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039131 | AAAGGGCCCTTGGGC[A/C]CTGAAAAATCAGCAG | 90293 |
rs764540858 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959924 | CAAGAAGGGAGTGCA[A/G]TTAGGTACAGAGGGA | 90293 |
rs764541826 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118062611 | AGTACAGTTGGGCCC[C/T]CACAGTCATATCCTG | 90293 |
rs764561399 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060488 | AAGTATACCTAAAAA[G/T]GGAAGCAGATGAAAA | 90293 |
rs764561797 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117971536 | TTTAACACCCAAAGA[G/T]ATAAAAATATCCTGG | 90293 |
rs764562434 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048854 | ACCTAATTGTAGTTT[C/T]GCCCTTAAAATATTC | 90293 |
rs764568620 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955496 | TTTTTGTAATGGCCT[A/G]GAGTCATCTCTAATT | 90293 |
rs764574889 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967688 | CTAGCTCTTTGTCTT[C/G]CAAGTGTCTTGTGTG | 90293 |
rs764580878 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117990738 | AAATGACACACAAGA[C/G]GGCCCAATGCGAACA | 90293 |
rs764582863 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:117980575 | GGTTAAAAATACTTA[C/T]AGAGTAATCAAAATA | 90293 |
rs764610678 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117947871 | TGCAAGGAGGTAACA[C/T]TTCTCTGCAAACCCC | 90293 |
rs764618069 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118115812 | CTTGGACTAAGTTAA[A/T]GAAACCTAGAAAGAA | 90293 |
rs764628313 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039818 | TCAGGTGGGACCCAG[G/T]GCAGTCCCAGTGGTG | 90293 |
rs764629854 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052500 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 90293 |
rs764630002 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063766 | ATTTCAAAAAGGTCA[C/T]TGTGAATTCTTAATA | 90293 |
rs764645342 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118090074 | CAACAGAGCAAGACT[C/T]TGTCTCAAAAAAAAA | 90293 |
rs764652732 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117929278 | AACACCAATACCCCA[A/C]AAACAAATCCAGAAT | 90293 |
rs764684320 | snp | C/T | 2.28133e-05 | 0.0033773 | missense | KLHL13 | GRCh38.p7 | X:117919607 | TGTCTTGAAGGTTGT[C/T]CATATTAAGAGAAAG | 90293 |
rs764696363 | in-del | -/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118101825 | GTTCCTCCTTCACTC[-/TT]CTCTCTCCTGCCACC | 90293 |
rs764702413 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074251 | AAACCCTCAACCATA[A/T]ATCTGTCAGCCCTTG | 90293 |
rs764710116 | in-del | -/G | 0.10695 | 0.205029 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118116866 | GAGGGAGGGGGCAGT[-/G]GGGGGGGGAGCGCGC | 90293 |
rs764717126 | snp | A/G | 0.0984496 | 0.198828 | intron-variant | KLHL13 | GRCh38.p7 | X:118052829 | AAGACGCCATCTCAA[A/G]AAAAAAAAAAAACTA | 90293 |
rs764762480 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099642 | AACACAGCAACACCT[C/T]GTCTCTAATAAAAAT | 90293 |
rs764763260 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913583 | GGGGGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 90293 |
rs764770794 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117953105 | AAAGACACATGCACA[C/T]GTATGTTTATTGCGG | 90293 |
rs764772062 | snp | C/T | 2.76778e-05 | 0.00371997 | intron-variant | KLHL13 | GRCh38.p7 | X:117910120 | CCAATTAAAAAAAAT[C/T]AAAACATGACTACTT | 90293 |
rs764773143 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002447 | AAAAATACAAAATTA[C/G]CCGGGCGTGGTGCTG | 90293 |
rs764774815 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027541 | TTTATTTCCATTTTT[A/T]CCATGAACTTTTAAA | 90293 |
rs764788374 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094098 | TAAAGGAGGAAGTTC[A/G]AACCTCCTCCTTTAG | 90293 |
rs764792954 | in-del | -/AAGAAA/AAGAAAGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089667 | AGAAAGAAAGAAAGA[-/AAGAAA/AAGAAAGA]AAAAAGAAAGTTTCA | 90293 |
rs764797736 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971197 | GGCTGCAATTTGGAT[A/C]TTTTAGACAATCAAA | 90293 |
rs764804714 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | KLHL13 | GRCh38.p7 | X:118020992 | TCTGGGGACTGTTGT[A/G]GGGTGGGGGGAGGGG | 90293 |
rs764813167 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950031 | ATTAGAGAAAAGCTA[G/T]AAAGGTAAAAGTATA | 90293 |
rs764816593 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118111805 | GCTGAGGTAGGAGAA[C/G]CGCTTGAACCCAGGA | 90293 |
rs764817785 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117943839 | TCTGTCAGTTTGTCA[A/G]ACTCATTCTCTGTCC | 90293 |
rs764820970 | snp | C/T | 0.124138 | 0.216007 | intron-variant | KLHL13 | GRCh38.p7 | X:118036470 | TGATCTTTGACTAAC[C/T]GGAGAAAAACAAGAA | 90293 |
rs764832551 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117920736 | TCTTAACATTCCTTT[A/T]CGCGATAATTTAATA | 90293 |
rs764833934 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117935834 | AGTTGCCATATTGAG[A/G]AAAGAGTTGGGGGCA | 90293 |
rs764850261 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093771 | ATGATGCCAAAAACT[G/T]GTTATTACAGGTTTT | 90293 |
rs764851870 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911489 | CGTACCATGGTGGTT[G/T]GCTGCACCTATCAAC | 90293 |
rs764863831 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117965158 | GATCCCTGAGGAATG[C/G]CCACACTGACTTCCA | 90293 |
rs764867794 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118057895 | ATACCTGACAATAAA[C/T]TATATGTAAGGATAT | 90293 |
rs764890359 | snp | A/T | 0.000159528 | 0.00892964 | missense, intron-variant | KLHL13 | GRCh38.p7 | X:117983504 | GATTTTTTGAATATA[A/T]CCTTGAAATCGGCTT | 90293 |
rs764894671 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006684 | AAGCATATTATCTCA[-/T]TAATTTTCAAGACAG | 90293 |
rs764896659 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935584 | AAACGTACAACCATG[A/G]CGGAAGGTGAAACAG | 90293 |
rs764923873 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922462 | CCATTAACGCATGAA[C/G]AAACAAACAAAATTT | 90293 |
rs764926699 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118003357 | CTGTCTCATTTTTTT[-/T]AAACTCTTTCTTCTA | 90293 |
rs764939527 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025791 | CAGATCAACAGTAAG[-/A]AAGAAATCTGTTGGT | 90293 |
rs764948930 | in-del | -/TTT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075988 | TTAAGTAAAAGCAAG[-/TTT]ATTAAGAAAGTAAAG | 90293 |
rs764956048 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107376 | CTACTCACCATTTAC[A/G]AGATGCACATTCGAA | 90293 |
rs764962951 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014664 | CAGAACCTGACGATA[C/T]GTGACTTCGCCTCCA | 90293 |
rs764971985 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902251 | ATAATTTGACATTTC[C/T]CCATTTTCTTTGCTC | 90293 |
rs764988596 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915962 | TCAGGAGTTTGAGAC[C/T]AGCCTGACCAACATG | 90293 |
rs764991265 | in-del | -/AGAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911970 | TGAGTCTCTAGAAAT[-/AGAC]AGCATAACACTGTAT | 90293 |
rs764995743 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903729 | GCTTTTAGAAGTAAT[C/T]AAACCACACATCCTA | 90293 |
rs765021580 | snp | A/C | 2.2941e-05 | 0.00338674 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117898986 | TGTGAGTGTGCAAGC[A/C]CGAATGCCACCAAGG | 90293 |
rs765043701 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118087064 | TCTCTTATTGAAAAT[A/G]AGAAAAATACAATAT | 90293 |
rs765045158 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956870 | CATCTTCAAAATCCA[A/G]TCTTTTCATATGTCA | 90293 |
rs765045597 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079319 | ACAGAATGAAAAAAA[A/G]GTAACCAAATAGGAA | 90293 |
rs765050640 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118112191 | TAAAACAGTATTAAA[C/T]GATCTAACATCAAAA | 90293 |
rs765073570 | snp | A/G | 0.0450304 | 0.143134 | intron-variant | KLHL13 | GRCh38.p7 | X:118036814 | AACAGGAAACCTAAA[A/G]AATGGGAGAAAATTT | 90293 |
rs765081689 | snp | A/G | 0.000317158 | 0.0125888 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028509 | TGACCTGTTCAGGAG[A/G]AAAAGAAGCCAATAT | 90293 |
rs765089205 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118105001 | TAGCTGTCAGTAAAA[A/G]GATTGTCAATTTGTT | 90293 |
rs765101297 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118077663 | GTTTTCTTCCATCAA[A/C]GTTGCTTCTGTTTGG | 90293 |
rs765102397 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117957676 | AAAAAATTCAGGACA[A/T]AAATGTAAATACTTT | 90293 |
rs765118968 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031671 | GTTATATATAATATA[C/T]ATAACTAAAATTTTT | 90293 |
rs765122200 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007542 | TCAAAAACAACATTA[A/C]ATTTAATTTGGATTC | 90293 |
rs765125536 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118001642 | GCTGAGGCAGGTGGA[C/T]TGCTGGAGCTCTGGA | 90293 |
rs765131425 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023426 | TATTCTTAAAAGGAG[C/T]ATGTAATTGTTTTCA | 90293 |
rs765141855 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968524 | CTAACACAAAATTTA[C/T]CTTAGGTGTTAGTTG | 90293 |
rs765154504 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072775 | TTTTCTCTTCCTGAT[G/T]AATTGAAGCCTATAT | 90293 |
rs765178646 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118003832 | CCCCTTCCTGAACAG[C/T]TCAATCCATTAGTGG | 90293 |
rs765185208 | in-del | -/A | 0.00105932 | 0.02299 | intron-variant | KLHL13 | GRCh38.p7 | X:118091278 | AACTTAAAGTATAAT[-/A]AAAAAAAGTATCAAT | 90293 |
rs765185720 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118049260 | GTAAGAAAAGAAAAC[G/T]GACAGAAAGGATTAG | 90293 |
rs765192442 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057028 | TTCCTTGGGACTTTT[A/T]TTCAGCAAAGATTAA | 90293 |
rs765209196 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118040849 | ACAATGGAGCTCCAA[C/T]ACATCTGTCAGCAGG | 90293 |
rs765209894 | in-del | -/CAATTTGG | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118018591 | GTAGAATGTATAGGA[-/CAATTTGG]AAATAATGTATCTCT | 90293 |
rs765210202 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978557 | TATAGTTGGGTGTCA[A/G]ATGAAAGAGGTTATG | 90293 |
rs765223040 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117949521 | TATAGTAAATATGTT[G/T]GTTGGAATGCTATAT | 90293 |
rs765223835 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941464 | GTGAATCCGTCTGGT[C/T]CTGGGCCTTTTTTGG | 90293 |
rs765232413 | snp | A/C | 3.29804e-05 | 0.00406068 | intron-variant | KLHL13 | GRCh38.p7 | X:117945598 | TTTTTTTACATAAGA[A/C]AGAAGGGGAAATTAA | 90293 |
rs765238998 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981176 | CAAACAGAAATTCAA[C/T]TAAAATCCTATGATG | 90293 |
rs765241039 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117917212 | ATTTCTACTCTAAAA[C/T]CATACAGACATATCC | 90293 |
rs765247160 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046521 | ACAACTTAGTTGTAC[A/T]TTTTAAAATAACTTA | 90293 |
rs765277071 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117932727 | TCCTTTGGATATATA[C/T]CCAGTAATGGGATTG | 90293 |
rs765281649 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933607 | TGGGCAAGGATTTTT[C/T]TAATAGGTCCTCAAA | 90293 |
rs765287100 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066392 | CAAAATACCAACTGG[A/T]GGCAATAACTCCTAG | 90293 |
rs765305943 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117954050 | CACAATAACAGATAT[A/C]ACACTATGACGTAGA | 90293 |
rs765308453 | snp | A/G | 2.28906e-05 | 0.00338302 | missense | KLHL13 | GRCh38.p7 | X:117945475 | TGCTGGTAAAGATGC[A/G]TGTAGGTCCTGCCTT | 90293 |
rs765339897 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118067990 | ATACCACTAGAAGCA[A/G]CACAGTGGGGTCGTT | 90293 |
rs765341527 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117908446 | CCCCTCCCTGTGACA[C/G]ACTCTATTTATAATA | 90293 |
rs765349120 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117931629 | CTTTGCTAATACATG[G/T]TTTTACATTTATAGT | 90293 |
rs765355761 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097742 | AGAGATATAGACCAA[C/T]GGAACAGAACAGAGC | 90293 |
rs765356053 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943554 | TTCTTTGATCTTGTC[C/T]TCTTGCTTTATTTCA | 90293 |
rs765364524 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108980 | CCCAGCTAATTTTTA[A/C]ATTTTTTTTTGTTCT | 90293 |
rs765364811 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118119024 | CTCTAAGATGGGCCC[A/G]AATCCAATATGACTG | 90293 |
rs765371746 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073161 | CTCCCTTCTCCCCTA[C/T]ATTAGTCTGTTTTCA | 90293 |
rs765372042 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924290 | AAGGCAGTCATTTCT[A/C]TAAACACCTTTTATT | 90293 |
rs765385279 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118033523 | AGAAATAAAATACTT[C/T]ACAGACAAGCAAATG | 90293 |
rs765411881 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963247 | ATAACCTCATCATAG[-/T]TAAGTTATGCTGGGA | 90293 |
rs765414614 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115610 | TTATCCCAAACCACT[A/G]AAGTCCTCTGACTAC | 90293 |
rs765451569 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118091958 | AAGTAACTCAGGAAT[A/G]GAAAACCACCAAACA | 90293 |
rs765462512 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118004129 | TTTCTTAATGTTACC[A/G]ATTGAGAAGTGAAAT | 90293 |
rs765472755 | in-del | -/TTC | 0.000529661 | 0.016265 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897565 | AGATATGGCTGGCAG[-/TTC]TTCTGTGGTGATGAA | 90293 |
rs765486348 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084094 | GGAGGCCAAGGTAGG[C/T]GGATTGTTTGAGGCC | 90293 |
rs765508381 | snp | A/T | | | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898187 | TGCCACTCAATTTTT[A/T]AAAAAATTATATTTG | 90293 |
rs765509582 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118054074 | AAATTGAGTGAAGAT[A/G]AAAAACTGCTGAGCA | 90293 |
rs765523266 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014540 | CTTGTGATCTTTTAT[C/T]GCCCTTTGAAGCATG | 90293 |
rs765527927 | in-del | -/CAAA | 0.000529661 | 0.016265 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898746 | ATAAACATTCTAGGC[-/CAAA]CAAAGAGCACAAATA | 90293 |
rs765539890 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077711 | CACATAACTTGGCCT[C/G]TTCTACTATCTGAGA | 90293 |
rs765541421 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974440 | ACTTAAATAGTTAGC[A/G]TTCGAATATTCTTTC | 90293 |
rs765548793 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117983280 | GAAAGCATGTTGGAA[A/G]ATATAAGGCACAATA | 90293 |
rs765548996 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004804 | TTATCAAGTTGTATG[G/T]GACAAATCAATATCA | 90293 |
rs765572260 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076920 | TTCTCTCTCTCTCTC[C/T]CCCTCTCTCCCCTTC | 90293 |
rs765579493 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924009 | CTGCTTTTGTAAGGT[G/T]TTACATTTATTTTCA | 90293 |
rs765580560 | in-del | -/TG | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118022209 | GAATAATATCCCATT[-/TG]TGTGTGTGTGTGTCA | 90293 |
rs765593612 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942346 | ATGTCTATTAGGTCT[G/T]CTTGGTCTAGAGCTG | 90293 |
rs765597165 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118038189 | TTTAGCCAATTAAGT[A/G]ACAAGTGAAGTGATG | 90293 |
rs765597720 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055615 | GGGGTTGCAAAAAAA[A/T]TTCAGTAATAAAGAT | 90293 |
rs765609882 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045909 | AATGTTGGCAAGGAT[A/G]TAGATAAAAGGAAAC | 90293 |
rs765611396 | snp | C/G | 0.10695 | 0.205029 | intron-variant | KLHL13 | GRCh38.p7 | X:118021702 | TCGCAATAAACATAC[C/G]TGTGCATGTCTTTAT | 90293 |
rs765612666 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069844 | CTATAGTAGTGTACA[A/G]TAATATCCTAGGCAT | 90293 |
rs765630455 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117988742 | ACCTCCCAATCCTAA[C/T]TGAATGAATCAGGAC | 90293 |
rs765654964 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117995580 | CAGAATGTTGCGCAA[C/T]CACCCCCTTCTATCT | 90293 |
rs765661990 | snp | G/T | 2.8607e-05 | 0.00378189 | intron-variant | KLHL13 | GRCh38.p7 | X:117909288 | TCTCTATGCTTAATA[G/T]AAATGCACTTACGCA | 90293 |
rs765670453 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965824 | GATTATCTCAATAGA[C/T]GCAGAAAAGGCCTTT | 90293 |
rs765687442 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032323 | ACAGCAGTAACCTCT[A/G]CAGACTTAAATGTCC | 90293 |
rs765691238 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904784 | GACAGAGATTTAATG[G/T]CCCACAAAGCTGGAA | 90293 |
rs765693597 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905499 | TGAGCACGTGTGCTA[G/T]TGCGTGCACACACAC | 90293 |
rs765695166 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027091 | TTGGGATGATCAAGA[C/T]GTTTTGCTTGAGGAT | 90293 |
rs765738524 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968342 | TGCAATGCCATCTTC[A/G]AGAGGTGTCATGGAA | 90293 |
rs765758151 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005462 | TCTTAATTCCTGGGA[C/T]CTATGCATATGTTGC | 90293 |
rs765761996 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118015885 | TATTTTTATTGGCTA[A/G]ATCTTCTAGCCAAAG | 90293 |
rs765788578 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938478 | GCCTTATCCCCAGAG[G/T]TTTTTATTAAAAAAT | 90293 |
rs765790441 | in-del | -/CCA | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118070917 | CCCCCTTCCCCCACC[-/CCA]CAACAGTCCCCAGAG | 90293 |
rs765791458 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118114357 | ACCAGATGGACTATC[-/A]AACACATATTGAGTC | 90293 |
rs765797176 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039017 | CATTCCAGGCCCTAG[C/T]TCCCAGATGACATTT | 90293 |
rs765837771 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088747 | GTCAAACTTCCTCTG[A/G]AAAGATGAGGTAGAT | 90293 |
rs765840043 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117938955 | GGATTTATTTTTTTT[A/T]TATACTTAAAGTTCT | 90293 |
rs765843009 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994177 | TTTGCACTTGTACAT[-/A]AGAGTTTAGTTTAAT | 90293 |
rs765851671 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117951324 | ATGTCATTTATAGTA[C/T]CATTACACAAAGAAA | 90293 |
rs765879164 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118105963 | CTGGAGTGCAGTAGC[A/G]CGATCTCAGCTTACT | 90293 |
rs765883097 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118032481 | CCCCAGCAGGGGCAG[A/C]CTGACACCTCACAGG | 90293 |
rs765887197 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117960557 | CAACAACCACATAAT[C/T]ATATGCCACTGCTAG | 90293 |
rs765910258 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052401 | GGTGGCAGGCGCCTA[C/T]AGTCCCAGCTAGGCG | 90293 |
rs765916266 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117980396 | ATTTTCTTCAACATC[C/T]CAATTTTAAATTAAT | 90293 |
rs765918355 | snp | A/T | 2.74326e-05 | 0.00370345 | intron-variant | KLHL13 | GRCh38.p7 | X:117910110 | ACCTATTAAGCCAAT[A/T]AAAAAAAATTAAAAC | 90293 |
rs765918821 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117987806 | GATAAAAGCTGTCTA[C/G]ACCTTCCTTCTTTTT | 90293 |
rs765922260 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118002324 | GATGGAGGCCAGGCG[C/T]GGTGGCTCACACCTG | 90293 |
rs765926443 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074473 | GCCAGGCCAGGAAAT[G/T]TTCCATGGATGTCCC | 90293 |
rs765928730 | in-del | -/AC | 0.00844535 | 0.064431 | intron-variant | KLHL13 | GRCh38.p7 | X:118051648 | CACTCACGCGCACAT[-/AC]ACACACACACACACA | 90293 |
rs765928859 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111991 | GCAAGTTCTATTACC[C/G]CTTTTTTACATATGA | 90293 |
rs765931653 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118026519 | ATTTATCACAAAGTT[G/T]GGGTGGAAGAATGAT | 90293 |
rs765933226 | snp | A/G | 0.0338441 | 0.125605 | intron-variant | KLHL13 | GRCh38.p7 | X:118089594 | AGAAAAGAAAAGAGA[A/G]AGAGAGAGAGAGAGA | 90293 |
rs765936061 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040273 | ACTAAATGAGGTACC[A/G]GAGACCAGTCTTAGA | 90293 |
rs765960828 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060113 | ACATAACAGAGCATA[C/T]AAATGCTATGAATGA | 90293 |
rs765974936 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117952002 | TTTATAGATTCAATG[A/C]CATCCCCATCAAGCT | 90293 |
rs765977607 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118001651 | GGTGGATTGCTGGAG[C/G]TCTGGAGTTCGAGAC | 90293 |
rs765984674 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117928883 | AAAACAGAAAAAGCA[A/G]TAAGACCAAAAGCTG | 90293 |
rs765985888 | in-del | -/CAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103309 | TACTAGCTGTGAGAT[-/CAC]CACACCTTTTGCCAT | 90293 |
rs765997647 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043474 | TCTGATGAACATTGA[C/T]GCAAAAATCCTCCAC | 90293 |
rs766005091 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089207 | CACACTCCTTTCTGC[A/G]CTGGGATGGGGTCAG | 90293 |
rs766011946 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059140 | TATTGTAGAAGCAAA[G/T]AGTTCTACAAGTCTC | 90293 |
rs766012772 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903500 | AAACTGCCACATGCC[C/T]CAGTACTGTTGTTTT | 90293 |
rs766018261 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089614 | GAGAGAGAGAGAGAA[-/AA]AGAAAGAGAAAGAAA | 90293 |
rs766020357 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081465 | TTTGGTTTTTTTTAA[C/T]TGATACATAATAATT | 90293 |
rs766023680 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019968 | TTAGGATTGACTTGG[C/T]GATGTGGGCTCTTTT | 90293 |
rs766045008 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117994449 | TAGAGATGGGGTCTC[G/T]CTATGTTGCCCAGGC | 90293 |
rs766093955 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118007031 | CCTTATTAGACTTAG[A/C]ACTGCTTCAGGGAAT | 90293 |
rs766102130 | in-del | -/T | 2.36894e-05 | 0.00344153 | frameshift-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117945561 | ATGTGTTGGTCTTCC[-/T]CTTCCACGAGAGATC | 90293 |
rs766111798 | snp | A/G | 0.111166 | 0.207907 | intron-variant | KLHL13 | GRCh38.p7 | X:118020437 | CAAATCAAAACCACA[A/G]TAAGATACCATCTCA | 90293 |
rs766112335 | in-del | -/T | 0.306401 | 0.243555 | intron-variant | KLHL13 | GRCh38.p7 | X:117971499 | TTACAAACTAGCCTA[-/T]TTTTTTTTTTACTTC | 90293 |
rs766112785 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956067 | TAAGATCACCATAAT[A/G]TTCCAGTCCATATCA | 90293 |
rs766115053 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117919181 | GGCATGCACCACCAT[A/G]CACAGCTAATTTTTG | 90293 |
rs766123862 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930852 | TCATAAAAACCACAA[G/T]AATCTAGACTATTTG | 90293 |
rs766148961 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986541 | AACTAAGCCTAGCAC[C/T]AAGAACTCAGTACAT | 90293 |
rs766165452 | snp | C/G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971966 | AACAATACTTTAAAA[C/G/T]AACATTTTATTATAT | 90293 |
rs766175340 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914106 | ATAACTGATGTACCC[A/G]AAACACTGTCATTAA | 90293 |
rs766177502 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933161 | TCTCCCATTCTGTAG[G/T]TTGTCTCTTCATTTG | 90293 |
rs766178668 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117964142 | GCACATGTATACATA[C/T]GTAACTAACCTGCAC | 90293 |
rs766199999 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118094064 | GAAGAAGGCTTCAGA[A/C]GATCAAACTACTCTG | 90293 |
rs766209645 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118067683 | GCACATAGGCCTACA[A/C]AGGGTCAGGATCATA | 90293 |
rs766216714 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118086263 | TAATGGCTTTTTTTT[C/T]CCCCTTTGGGTAGAT | 90293 |
rs766228854 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902060 | GAAACATATCTATTA[C/T]AGCTATGATAGATAT | 90293 |
rs766255527 | snp | A/C | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118057825 | AGCGAGAGTCCATTT[A/C]AAAAAAAAAAAAGTG | 90293 |
rs766268156 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118058600 | GCTGGTCATGAATTT[A/G]TCACCCAAAATATTT | 90293 |
rs766270896 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117956808 | ATGCTACTACCCTCA[C/T]TCACTCCATCTCCAT | 90293 |
rs766276659 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118036148 | AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 90293 |
rs766277943 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017790 | ATATTTGTTAAAATG[A/G]TAAAAATATGATTGT | 90293 |
rs766279727 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041544 | AAAAAGAAAAGAAAG[A/G]GACAACAAAAAGTTA | 90293 |
rs766298245 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117976818 | TCAGAGACGTAACAA[A/T]CAAAGGACAATGATG | 90293 |
rs766303329 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117964776 | CAGAGTGTGATGTTC[C/G]CCTTCCTGTGTCCAA | 90293 |
rs766326482 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118078546 | CTCTTTTAGTTGATT[A/G]GCATTAACGCCTTTG | 90293 |
rs766337351 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117949333 | GTGGTTTTTTTTTAA[C/T]AGCAAGCAACATGAC | 90293 |
rs766340239 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111747 | AATACAAAAAACTAG[C/T]CTGGCGTGGTGGCAC | 90293 |
rs766345668 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023745 | AGCTAATTTTCTTTG[C/T]ATTTTTAGTAGAGAC | 90293 |
rs766354654 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117905265 | TATTAATATTTAACT[A/G]AAGTGAAAGATATTG | 90293 |
rs766356987 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006544 | AAAAAAAGTGTAGTA[C/T]GTTATTTGTGGAGCC | 90293 |
rs766362448 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036438 | CTCAGAAACAACGCC[A/G]CATATCTACAACTAT | 90293 |
rs766377607 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117947432 | GACCATCAATTATCA[C/T]TCTTATGAAACTGCA | 90293 |
rs766414885 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939898 | CTGTAGGATTCCTGT[A/T]CACTCTGATGATAGT | 90293 |
rs766414980 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118084553 | ATTTATAAATGCACA[C/T]GCCTTTTGCTGCAGA | 90293 |
rs766452430 | in-del | -/T | 0.112567 | 0.208835 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031539 | TTAGTTATATATATA[-/T]TTAGTTATATATATA | 90293 |
rs766458161 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961762 | TAGCCAACAAGATGA[C/T]AGGAACCTTGGTCCT | 90293 |
rs766460421 | snp | C/G | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029133 | TTTATACAGGAAATT[C/G]GAATAAACTGAGAAT | 90293 |
rs766472343 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083136 | GGTATTTTGGTAGGA[C/T]TGCATTGACTCTGTG | 90293 |
rs766491772 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959088 | TACTGCACATCATTT[-/A]AAAAAAACACTCTAA | 90293 |
rs766496452 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117999144 | AACAAAAGGTTCCTC[A/G]GGGATCTAGAACTAG | 90293 |
rs766506163 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079857 | GAAAAAAGCCAGAGG[A/C]ATCACACTACCTGAT | 90293 |
rs766525024 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117960615 | TTTAAGGTTCTCAAC[A/G]ACCTGTATTATTTGA | 90293 |
rs766525570 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040742 | GATTTAGCTCAAAGA[A/C]GACCACCTCAAGGCA | 90293 |
rs766527107 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117940982 | CTTCCAATACTATGA[C/T]GAATAGGAGTGGTGA | 90293 |
rs766533629 | snp | A/G | 2.28042e-05 | 0.00337663 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909791 | TTGCACGTAATTAAT[A/G]AGCTCCTGTGGTGTC | 90293 |
rs766544033 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118105390 | GTTCTTATACATATT[A/C]GGTGTGTAACCACAG | 90293 |
rs766547094 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118024483 | GCCATGGACTGGAAG[A/G]AAATATTCACAGTAC | 90293 |
rs766569643 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051831 | ATTGGGAGAACTGAA[C/T]ACATAAAAATTGTCC | 90293 |
rs766578414 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942217 | ATGATTTCTGTTCTT[A/T]TACACTTACTGAGGA | 90293 |
rs766597174 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118011595 | TGAATTGGAGAAATA[A/C]TTGGGAAGGAGAAGT | 90293 |
rs766603235 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117931504 | TTTTTCTCTTTTCAG[C/T]AGGTGAACGGAAGAA | 90293 |
rs766620612 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118091070 | ACTCATAGGTGGAAA[C/T]TGAACAATGAGAACA | 90293 |
rs766621155 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999786 | CAACACATGGTGAAT[A/C]TGAAGCTGAGGGCCA | 90293 |
rs766621270 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991106 | TGTTTTTGGGGTATG[C/T]TTGGAAAGGCTGGAA | 90293 |
rs766624343 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118033469 | GAATTTTCAACCCAG[A/C]ATTTCATATCCGGCC | 90293 |
rs766625639 | in-del | -/CT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991855 | AGTGAAACTCTCTCT[-/CT]CTCTCTCTCTCTCTC | 90293 |
rs766635182 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118018495 | ACAATGTACTAATAA[C/T]GGAGATACATTTCTT | 90293 |
rs766641112 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108142 | ACCATTTTTTTAAAA[A/G]TGGGACCAAGAAAGA | 90293 |
rs766665236 | in-del | -/G | 0.0850455 | 0.187856 | intron-variant | KLHL13 | GRCh38.p7 | X:118053849 | AGAGAGAGAGAGAGA[-/G]GAGAGAGAGAGAGAG | 90293 |
rs766669949 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117982596 | GAAAAGTTCTTTACC[A/T]TTAAGGCAGATGTGC | 90293 |
rs766672810 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083520 | ACTCATAATGAGGAA[-/T]TTTTTAAGTTTATCT | 90293 |
rs766680242 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118072674 | AAGTGGGCGAAGGAC[A/T]TGAACAGATTTGTCA | 90293 |
rs766706570 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093526 | GTTCGAGTACCATTT[C/G]ATGTAATGAATACAC | 90293 |
rs766710046 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029296 | TGGGGTCTGAGAAGT[C/G]TATAAACAGGGAACA | 90293 |
rs766732918 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115369 | TAACACCACAACTAC[A/T]TGGGGAGAAAGCGAT | 90293 |
rs766735204 | snp | A/C/G | 9.16674e-05 | 0.00676956 | missense | KLHL13 | GRCh38.p7 | X:117899320 | ACAGTGGTCATTGGC[A/C/G]CCTTCTGGATCCATT | 90293 |
rs766736903 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117925164 | TAATTTGTATAAAAA[C/T]TACTTGGATGTCAAT | 90293 |
rs766761903 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922034 | TTATATATCCTATGC[C/T]ACTATTTTTATTTTC | 90293 |
rs766764810 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076132 | CAACAGTTTTTGTCC[C/G]TTCTATTTCTTCTTC | 90293 |
rs766769131 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014242 | TTTTCCCAGCAAGGA[A/C]TATTAATAATTGGGA | 90293 |
rs766769670 | snp | C/T | 0.00112909 | 0.0237333 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973437 | CTAAATTCAGCAGCC[C/T]GCTTTCCTCCTGTGC | 90293 |
rs766779638 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974201 | TTATGCTGAACTGTT[G/T]ATTTACAGGCTGAAG | 90293 |
rs766788476 | snp | C/T | | | missense | KLHL13 | GRCh38.p7 | X:117909832 | ATCGTATGTTCTTCA[C/T]TAATTTTGCAGCAAA | 90293 |
rs766816355 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028664 | AATTAAGAAATTGAA[C/T]CTTATTTAAAAAACT | 90293 |
rs766821110 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118109659 | ACCCTGCTCAATCAG[C/T]ACATGTGCTCCACTT | 90293 |
rs766844424 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117990429 | TTTATTAGTTTGTTA[A/C]CACCTAGGCCAGGGA | 90293 |
rs766848767 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076841 | AAAATCTTTTTTCTC[C/T]TTCTTTTCTTTTCTT | 90293 |
rs766854091 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924097 | GAATGACCCCACTAT[A/C]CAATTCCATATTAGT | 90293 |
rs766858944 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117965305 | TGAGACAGTATCTCA[C/T]TGTGGTTTTGATTTG | 90293 |
rs766862753 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004729 | AAATACTATTAATTA[G/T]AAATAAAAGAAAAAG | 90293 |
rs766897231 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117937510 | TTGTCAGCTGTTATA[C/T]ATTTTTTTATTACAG | 90293 |
rs766914036 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965677 | ACTGGCAAACGGAAT[C/G]CAGCAGCACATCAAA | 90293 |
rs766916587 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023719 | AATTACAGGTGTGCA[C/T]CACCATGCCTAGCTA | 90293 |
rs766916712 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045811 | GACTCTGTCTCCAAA[A/C]AATAAAAATAAAAAT | 90293 |
rs766919196 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118067491 | CTTAGCTTACTGTAA[A/C]TTTTTTTATATGCTT | 90293 |
rs766969851 | snp | A/T | 4.58327e-05 | 0.00478688 | missense | KLHL13 | GRCh38.p7 | X:117945453 | AACACCACAGAACTG[A/T]GGGTATTGCTGGTAA | 90293 |
rs766989908 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118094781 | CAGAATTTCATATCC[A/G]GCCAAACTAAGCTTC | 90293 |
rs766997692 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118079778 | TTATTCTTCACAGAA[C/T]TAGAAAAAACTATTC | 90293 |
rs766998647 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118006725 | TTCTGTTCTAAAAAC[A/G]AAAAAAAAGGAAGAA | 90293 |
rs767004554 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044250 | ACAACAAAATGGAAA[C/G]ATATTTCATCTTCAT | 90293 |
rs767004615 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117945783 | AGTACAGAATATACA[A/G]ATGATAACTGAGAAA | 90293 |
rs767009006 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997499 | AAAACAAATGAACAA[A/C]AATCTGTCTTCAAGC | 90293 |
rs767019533 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | KLHL13 | GRCh38.p7 | X:117899273 | TGACATAGAGCCTTT[C/T]TCCCACTGTACACAT | 90293 |
rs767025447 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113395 | TTCCTATTGTTCTGA[G/T]AATCAAACCCAAATT | 90293 |
rs767027046 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117903524 | TTGTTTTTTTTTACT[A/G]TTTCCAGTCACTGGA | 90293 |
rs767027835 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118061155 | ACCTTAAGTGTTTTT[A/C]AATCATAAATAAAAT | 90293 |
rs767049653 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117938395 | CCACCTCTAGAACAA[C/T]GGTCTTAAAACTATG | 90293 |
rs767056214 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060050 | AATATAAATATGAAC[A/G]AGGAACAGTACCTAC | 90293 |
rs767058819 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008945 | CCTAGTACAAAGTAA[C/T]GCTATTTAAGTGTTA | 90293 |
rs767064951 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080808 | AAAAATACACGTGCA[C/T]TTGTATGTTCATCAT | 90293 |
rs767082236 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015747 | GATAAATTTCATGTG[C/T]GTCTACCATAAGATC | 90293 |
rs767086366 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118095537 | AGCCCTGCACCAAGC[A/G]GACCTAACAGACATC | 90293 |
rs767094907 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927198 | AGCTACCGCGCCCGG[A/C]CACTTCTTTCTTAAA | 90293 |
rs767102138 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032284 | GGCTCCACCTCTGGG[A/G]GCAGGGCACAGACAA | 90293 |
rs767109470 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005357 | CAGCCATTATCTTAA[C/T]ACCCTCCAAAAGAAA | 90293 |
rs767113969 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954792 | TAGGCCCTCTAGAAG[A/G]ATGCTTCGCCCTACA | 90293 |
rs767120488 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078154 | TCCTTATAGTTTAGC[A/G]TCACCTGTAGCAGTT | 90293 |
rs767131565 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950544 | TTTCAAGTTCCCCAG[A/G]TTAATAATATTACCT | 90293 |
rs767177924 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118088584 | TGCCTACATAATGAT[-/A]ACTTTAAATAACTCT | 90293 |
rs767181471 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117918796 | ATTCTTACAGGTTTG[C/T]CCATAGGTATTAGTT | 90293 |
rs767191935 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032467 | AACTGGGAGGCACCC[C/G]CCAGCAGGGGCAGCC | 90293 |
rs767219893 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928587 | AAATGTTTTGAAACT[A/G]AAACATACTTCTAAA | 90293 |
rs767221068 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994440 | TATTTTTTTAGAGAT[-/G]GGGGTCTCGCTATGT | 90293 |
rs767229275 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050760 | TCCACTGAGCCCTGA[A/T]ACACACACATCTTGC | 90293 |
rs767253268 | snp | G/T | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118098419 | TCATTAAAAAGTCAG[G/T]AAACAACAGGTGCTG | 90293 |
rs767255651 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025178 | CTGTGAGCAAGTCTG[C/T]TTTACAGCCCCTAAG | 90293 |
rs767258593 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941577 | TGGGAGGGTGTATGT[A/G]TCTAGGAATTTACCC | 90293 |
rs767316972 | in-del | -/A | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118051540 | GTGAGACTTCATCTC[-/A]AAAAAAAGTAATAAA | 90293 |
rs767352663 | in-del | -/TAAC | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093284 | AGTTATATAAAATAA[-/TAAC]TAACATTTATTAAAT | 90293 |
rs767361634 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117910224 | TAGATACAAATAGGA[C/T]TCTTATCTAAATGTA | 90293 |
rs767371006 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074193 | AGAACACTATGACCT[C/T]AGCAGAAATGTAGGT | 90293 |
rs767382489 | snp | C/T | 2.6454e-05 | 0.0036368 | intron-variant | KLHL13 | GRCh38.p7 | X:117910100 | GTCTAAAGTGACCTA[C/T]TAAGCCAATTAAAAA | 90293 |
rs767385082 | in-del | -/AA/AG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089588 | AGAAAAGAAAAGAAA[-/AA/AG]AGAGAGAGAGAGAGA | 90293 |
rs767386978 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118092699 | AATTTATGTCTCTTA[C/T]GGTGAAATATTTCTG | 90293 |
rs767396225 | in-del | -/CA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948134 | AAACATCCTACAAAA[-/CA]CAGGACAGTTCTCTA | 90293 |
rs767398929 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903192 | AGCGAGAGAGAGAGA[C/G]AGAGAGAGAGAGACT | 90293 |
rs767408502 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994359 | CCTGGGCTCAAGTGA[C/T]CCTCCCACCTTAGTC | 90293 |
rs767409339 | snp | A/C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088891 | TCAGGACCCAAGGAA[A/C/T]AGCACAGTGGAGATT | 90293 |
rs767409396 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118019859 | TGATCTATATCTCTG[-/T]TTTGGTACCAGTACC | 90293 |
rs767417845 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118035242 | CCCTAACTCATTTTA[G/T]GAGGCCAGCATCATT | 90293 |
rs767432176 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | KLHL13 | GRCh38.p7 | X:117964098 | CCTAATGCTAGATGA[C/T]ACGTTAGTGGGTGCA | 90293 |
rs767438406 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039120 | ATCTGCTGATTAAAG[A/G]GCCCTTGGGCCCTGA | 90293 |
rs767441480 | snp | A/C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117965457 | TGTTGTAAATTTGTT[A/C/T]GAAATTCTACCAGAG | 90293 |
rs767449910 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971455 | TTTTGACAAACAGTT[C/T]TTGAAAAACAAATAT | 90293 |
rs767452894 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118014068 | AATATTAAATCAGTG[C/T]ACCCTAAGAAAGAAC | 90293 |
rs767460844 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117900968 | AACAATTTGAGAATG[A/G]AAGTTGCTACTGGGA | 90293 |
rs767464395 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092001 | ACTCATATGCGGGAG[C/T]TAAGCTATGAGGATG | 90293 |
rs767476851 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084862 | GAAACCCCATTCTAC[-/T]AAAAATAGAAAAATT | 90293 |
rs767492491 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968143 | CACATGAGAAGACGC[C/T]TAAGCGTGTATGTAA | 90293 |
rs767493615 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118016523 | GGTACAACTTCTACA[C/G]GTATTTACTGAAAGC | 90293 |
rs767497245 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043424 | CCAAAACCAAACAAA[C/G]ACACATCACAGAAAG | 90293 |
rs767498098 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117976700 | GGCTTCTATTATGTA[C/T]AATTGCATAAAACAG | 90293 |
rs767502551 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:118067563 | GCTTAAAACACATTA[C/T]ACAGCTGTAAAAAAT | 90293 |
rs767504203 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047553 | TTAGGTTGGTGTGAA[A/G]GCTATTGCAGTTTTT | 90293 |
rs767519661 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118110648 | TCCTTAAGTGCTGGT[A/G]TTACAGGCGTGAGCC | 90293 |
rs767535138 | snp | A/C | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985669 | CACCAGGAAATCCAA[A/C]TTAGAAAAAAAAACA | 90293 |
rs767542047 | snp | C/T | 2.31967e-05 | 0.00340556 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909992 | CCCTGTGCTCAGCAA[C/T]GCAGGAAAATTCTTC | 90293 |
rs767553177 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998536 | CAACTACCCCTAGGG[C/G]TGAGAAAGAGCACCA | 90293 |
rs767560846 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900806 | GTCAGGGCCAAATGA[C/T]AATAACCTGACTAAC | 90293 |
rs767571037 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957224 | TCTTACCTGGATTTA[A/G]TTATAATTTTCACAT | 90293 |
rs767574754 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118013644 | GTAAAGAGAGGATTT[C/G]ACACAGTATAGAGCA | 90293 |
rs767596640 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118057709 | CGGACACCTGTAGTC[C/T]CAGCCACTCGGGAGG | 90293 |
rs767601822 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103660 | ATAATAGAAAGGAAA[C/T]AGTAATTATTTAGTC | 90293 |
rs767613057 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026750 | CAGACATGATACCCA[-/AC]ACCATAGATACCACA | 90293 |
rs767642213 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979878 | ACCTGTTTAGTCATC[G/T]CTCAGCAACTTCCTA | 90293 |
rs767672412 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085432 | TAAAAGGAGATAGAT[-/AT]ATATATATATATTTC | 90293 |
rs767672865 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040537 | GAAAAAATAAAAAAG[-/A]ATAAAGTATACTTAC | 90293 |
rs767685689 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081582 | CCTCAAACATTTATC[A/T]TTTCTTTGTGCTGGG | 90293 |
rs767686695 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948032 | TCAATGTGGGGAGGG[A/G]GAGCAGGAGGCATTT | 90293 |
rs767703201 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924918 | AATGTTTTAATGTTT[A/C]ATGTTTAATGTTTTT | 90293 |
rs767716862 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118096975 | ACAGCCAATATCATA[A/C]TGAATGGGCAAAAAC | 90293 |
rs767729354 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118023697 | CCTCAGCCTCCCAAA[C/T]AGCTGGAATTACAGG | 90293 |
rs767732636 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073949 | TACCCTTAACATACT[G/T]TATAAATGAGGAAAC | 90293 |
rs767738781 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048440 | AGGAAAATGCAATTG[C/T]GGAAGGATACTCTAG | 90293 |
rs767741675 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939734 | GTTGGACACATAAAT[A/G]TGTTCTTTTGAGAAG | 90293 |
rs767750967 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999077 | CAAAACTTCAGTGTC[A/G]GGTGGTAATGGAAGC | 90293 |
rs767765968 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040603 | GGAGTTATTGGCATT[A/C]AAGAAGTGGTAGATA | 90293 |
rs767777579 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118096570 | GGGAATCCTCCCTAA[C/T]TCTTTGATGAGGCCA | 90293 |
rs767780352 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991603 | ATCTATTCAACCCTA[C/T]TTCCCATTACAGGTA | 90293 |
rs767787586 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049593 | AGTGGTGATTCTTCA[C/T]TACAGTAAATCTAAA | 90293 |
rs767790225 | in-del | -/CA | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118063862 | TACTTACAAAGAGAG[-/CA]CAGTCTTATCTTTTG | 90293 |
rs767802795 | in-del | -/TG | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118082584 | TGATTGTTTCCTAGC[-/TG]TGTAGAAGCTTTCTA | 90293 |
rs767804027 | in-del | -/AAAC | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118115949 | TAGTCAACTGTAATT[-/AAAC]AAACAAACAAACAAA | 90293 |
rs767811009 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118011451 | GAGAAACTGTCAGGG[A/G]AGAAGGGGAGGGCTA | 90293 |
rs767811131 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118090168 | ACTTAAATGTTAGAC[C/T]TAAAACCATAAAAAA | 90293 |
rs767817339 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118018110 | TAAAGCACTAGAATA[A/G]AACTTCATATAGGGT | 90293 |
rs767818096 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998488 | AGATTCTAAAAAAAA[A/C]CACAAGAATCAAAGA | 90293 |
rs767822500 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968369 | GGAATGAGTTCCTGT[C/G]TTAAAAGGGGTTTGG | 90293 |
rs767826547 | in-del | -/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118040127 | TACCTGGAAAGCCTT[-/C]CCAGGAAGGATGAGT | 90293 |
rs767827755 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922620 | GTGCTTAAAGTGTTC[A/G]TTTGTGTTCGTTTGT | 90293 |
rs767832879 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071090 | AGGACATGAACTCAT[C/T]ATTTTTTATGGCTGC | 90293 |
rs767851537 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118062752 | TTCCCACTAATTAAA[A/C]AAACTGCTACAAAAT | 90293 |
rs767867863 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117989921 | TGTCTCCCTAGACTA[C/T]AAATTCCTGAGAACT | 90293 |
rs767873165 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981308 | CTATCCAATGAAAGG[G/T]AAATCATTTCTTTTC | 90293 |
rs767874031 | snp | A/C | 0.114895 | 0.210349 | intron-variant | KLHL13 | GRCh38.p7 | X:118010372 | TAGACTGGATTAAGA[A/C]AATGTGGCACATATA | 90293 |
rs767874606 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082910 | ATCAGTTGGCTGTAT[A/G]TATGTGTATTTGTTT | 90293 |
rs767875617 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117978090 | CTACATTGGAAAGTT[C/T]TACATTAGAAATTTC | 90293 |
rs767876020 | snp | A/C | 0.000617623 | 0.0175622 | intron-variant | KLHL13 | GRCh38.p7 | X:117920377 | GTCAAAGCCCTACAA[A/C]AAGAACATGAGTTGA | 90293 |
rs767878202 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117990917 | ACTGGTGGAGGAGAA[A/T]TATCAAGAATATTTA | 90293 |
rs767881307 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924071 | TAACCTTTATTTTTA[C/T]ATGCATAAATGAATG | 90293 |
rs767881402 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113846 | CAAGAGCAAAGATCA[G/T]GCCTTATAAGGTTTA | 90293 |
rs767895280 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118003151 | CTTTTTGAACTCATG[C/T]TCCTAACCCTAAATA | 90293 |
rs767897315 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959203 | TTGTTTCCAGTTTCA[C/G]GAACTTTGTTTAGCT | 90293 |
rs767908903 | in-del | -/AAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085026 | AGACTCTGTCTAAAA[-/AAT]AATAATAATAATAAT | 90293 |
rs767922580 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071314 | ATTTCTAGTTCTAGA[A/T]CCCTGAGGAATCGCC | 90293 |
rs767942158 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117988462 | AAATATCCATAGTGA[A/T]AGATTTTGAGAACCA | 90293 |
rs767970454 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944090 | AACAGGCCCCTCTGC[C/T]GCAGATCTGCTAGAG | 90293 |
rs767980882 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118012672 | AAAATGTGGCCATCC[G/T]GGGCGGGGGCGGGGG | 90293 |
rs767981264 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008749 | TGCAAAGACTCTGGA[A/G]CTAGACTTCCTGCAT | 90293 |
rs767986824 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117933368 | ATCCATGTATTTACA[A/G]CCAAGTGATTTTTTT | 90293 |
rs767987836 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118032967 | CTCAGGAGCCGATGC[A/G]ATCAAATGGAAGAAA | 90293 |
rs767990513 | snp | A/G | 3.29495e-05 | 0.00405877 | missense | KLHL13 | GRCh38.p7 | X:117899075 | CTATCTCTACCATAC[A/G]ACGATTATTCCAAGA | 90293 |
rs768001623 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117982121 | CATGTTCCCTGGCCA[C/T]AAGACCATTATAATC | 90293 |
rs768016656 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961677 | CAACCTGCTGTCGCT[C/G]GCCTTAACGAGGGAG | 90293 |
rs768018867 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117952135 | AGCTGGAGGCATCAC[A/G]CTACCTGATTTCAAA | 90293 |
rs768027409 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014931 | AATCTAATAAGAAAA[-/A]CAGGGAGGTACAGAC | 90293 |
rs768036139 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118055076 | AGGTCACTCTACTTT[C/T]ACTGTGCAAGGGATT | 90293 |
rs768044632 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118012099 | TTGCTTTTTAAAGCA[A/G]CCAGAGTTCTAGTAC | 90293 |
rs768048817 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044339 | CAATGTAACCCCTAT[A/C]AAAATACCAATGACA | 90293 |
rs768063894 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118065065 | CTGGATCGACAAGAC[G/T]TTCACTATGTGGATG | 90293 |
rs768070703 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004532 | AGACTTGTGAAAAAG[A/G]TACATAAACCAGCTT | 90293 |
rs768073995 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953119 | ACGTATGTTTATTGC[A/G]GCACTATTCACAATA | 90293 |
rs768075982 | in-del | -/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118033133 | TGTACCTGAAAGTGA[-/G]GGGGGGGGAATGGAA | 90293 |
rs768082174 | in-del | -/AC/ACAC | 0.0589768 | 0.162506 | intron-variant | KLHL13 | GRCh38.p7 | X:118027648 | TCTCTCTCCACACAT[-/AC/ACAC]ACACACACACACACA | 90293 |
rs768089764 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083972 | GTACAAATGGAGAAA[C/T]AATAAAAAACAAAAA | 90293 |
rs768108935 | in-del | -/AGA | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118053812 | GTGAGAGAGAGAGAG[-/AGA]GAGAGGAGAGGAGAG | 90293 |
rs768133892 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076054 | ACCAGTTTCTAATTT[A/T]ATGTTTATTTGAGCA | 90293 |
rs768144567 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117945666 | AATCAGTCACTATTG[A/C]AATCATATGACCATG | 90293 |
rs768147346 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118108682 | TAAAGTTAGCAAAAG[C/T]GAACTTCAAATCAGT | 90293 |
rs768155802 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118063091 | TTGGGGTTAAGGGAT[G/T]ATCTAAATAGATATG | 90293 |
rs768169737 | snp | A/G/T | 4.61162e-05 | 0.0048017 | missense, synonymous-codon | KLHL13 | GRCh38.p7 | X:117945524 | TGAGAGGCCCATTTC[A/G/T]CTGCCTCCAAGGGAC | 90293 |
rs768176568 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974531 | ATTTTAGAAACACAC[A/T]TGAATGTTTCTACAG | 90293 |
rs768179551 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084372 | ATAATAGTGACAAAC[-/T]TCTTAAAAGACTGAT | 90293 |
rs768186897 | snp | C/G | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117670 | CTGCTTCCAAACTCT[C/G]GTGGGACTGCTCTTC | 90293 |
rs768187770 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910873 | CTGTTTCTCTCTGGC[A/G]TCAACATGAGCCCAG | 90293 |
rs768189604 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117993031 | AGTCACAGTACTATA[C/T]AAGCTATGCTATAAA | 90293 |
rs768210407 | snp | A/G | 2.28045e-05 | 0.00337664 | missense | KLHL13 | GRCh38.p7 | X:117899257 | AAGTGATTGCCACCA[A/G]TGACATAGAGCCTTT | 90293 |
rs768218723 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118101417 | TCCTCAAGGAATTCA[C/T]AATCCAGGGAGAGAG | 90293 |
rs768230691 | snp | A/C | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118045795 | TTGGGCAGCAGAGTG[A/C]GACTCTGTCTCCAAA | 90293 |
rs768255055 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078120 | AAAGTATTTAATTAG[C/T]AGACGCAGCAGAAGG | 90293 |
rs768255595 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029202 | AAGAGAAGTTAGAAG[C/G]GGGGAGTTGAGGCAA | 90293 |
rs768270449 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024793 | AATGGTACAACTATT[C/T]TCAAAAAACGTTTGG | 90293 |
rs768303128 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087835 | AATATAGTGGCCCCA[A/G]GATCAGAGAATCTGA | 90293 |
rs768316752 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118037871 | GAGATAAGAGCCCAG[A/G]CAATGTCTATGAGGA | 90293 |
rs768318462 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047005 | ATAAATAAATTATTT[C/G]AAGATCTTGTGAGGA | 90293 |
rs768323098 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118101680 | AATTTATAATCCCCA[A/T]GTGTGGAGGGAGGGA | 90293 |
rs768323960 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118077359 | CGTTTGGGGCTGGTC[C/T]TTAAGGATGGATGAG | 90293 |
rs768337690 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046499 | ACAGGAGCAACTATA[A/G]TTAATAACAACTTAG | 90293 |
rs768342143 | snp | A/T | 0.080205 | 0.183493 | intron-variant | KLHL13 | GRCh38.p7 | X:118095302 | ACAAAGAAGGCCATT[A/T]CATAATGGTAAAGGG | 90293 |
rs768357238 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089253 | GAGCCAGGACTTTCA[A/C]CACTATCCAGTGGCT | 90293 |
rs768365670 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117966220 | AGCAAAGTCTCAGGA[C/T]ACAAAATCAATGTGC | 90293 |
rs768376577 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955481 | AAATCTCAGTCTTGA[A/T]TTTTGTAATGGCCTG | 90293 |
rs768389774 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118032458 | AAGCAGCCTAACTGG[A/G]AGGCACCCCCCAGCA | 90293 |
rs768393671 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926886 | GAAGCCCCCTACTTC[-/TTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 90293 |
rs768402276 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113965 | CCTGATTGTTATGAA[C/T]ATCAGTAACTTGAGA | 90293 |
rs768404806 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118067318 | GCATGAATGGAACCT[G/T]CAGGACTGGAAGTTG | 90293 |
rs768407444 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994989 | AGAGTTCAAGGCTGC[A/T]ATGAGCTATGATGGT | 90293 |
rs768407550 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117998018 | CGCTGCCTCACCAAG[A/G]CAGAAATTGAGACGC | 90293 |
rs768412991 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102222 | CAGATAAGTCAAAAA[A/T]TGATGAATGATTAAA | 90293 |
rs768421422 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997281 | AATTTTTAAACAAAA[C/T]GTTTCCCTTTTTAAA | 90293 |
rs768425526 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069627 | TATGTATATATGTAC[A/G]GATATAAAAAAAGAA | 90293 |
rs768425652 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045744 | CCCGGGAGGCAGAGA[C/T]TGCAGTGAGCTGAGA | 90293 |
rs768432331 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008142 | TAACCCAAAATAGAA[C/T]ATTACACAACTGTTG | 90293 |
rs768435254 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927063 | GGCGCATGCCGCCAC[A/G]CCCGGCTAATTTGTA | 90293 |
rs768440915 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975665 | CAAAGTGCTGGGATT[-/A]AAGGCGTGAGCCACC | 90293 |
rs768441006 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117960185 | AGGCTAGGAGTTCAC[A/G]ACCAGTCTTGGAAAC | 90293 |
rs768445043 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081411 | AATATCTATAAAAAA[A/G]TAAGAATACAAATAC | 90293 |
rs768474779 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117988511 | AGCCAGGAGTATTTA[C/T]ATTGGAAGCAATTGC | 90293 |
rs768475293 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959655 | CACATTCTCTTTCAA[A/G]GTAAATGGTATGACC | 90293 |
rs768479436 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118026305 | GAGGGATCTTCAAAA[A/C]GTTCATGCAAAATGT | 90293 |
rs768488193 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117928611 | TTCTAAATAACCCAT[A/G]AAGAAATCAAAAGAA | 90293 |
rs768491897 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951765 | AAGATCATTTACCCA[C/G]CACCTGCTGTGTACT | 90293 |
rs768492191 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118115249 | TGCGTATGTCAGCAT[A/G]TGCTTGTTCACTGGT | 90293 |
rs768499256 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118095812 | TACATAATGAAATGA[A/C]GGCAGAAATAAAGAT | 90293 |
rs768513244 | snp | G/T | 2.51629e-05 | 0.00354695 | intron-variant | KLHL13 | GRCh38.p7 | X:117899440 | AAATAATTATAGAAA[G/T]GCAAAAGTAATTAAA | 90293 |
rs768516259 | in-del | -/GTTTT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971271 | CCTGATTTTAGTGAG[-/GTTTT]GTTTTGTTTTGTTTT | 90293 |
rs768517992 | snp | A/C | 2.28613e-05 | 0.00338085 | intron-variant | KLHL13 | GRCh38.p7 | X:117920227 | TTTCAGAGTTTTAAA[A/C]GGCAAACTACCTGTG | 90293 |
rs768519379 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118102773 | ACCTACATGCAGAGT[C/T]ATTCTAAACCATTTA | 90293 |
rs768525046 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905368 | AGATGCCAGAAATAA[A/C]TGACTCCTTTTACAC | 90293 |
rs768551598 | in-del | -/GGAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954411 | GATAGGTAGACGGAT[-/GGAT]GGATGGATGGATGGA | 90293 |
rs768556835 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059921 | GAGCACTTAACTACC[A/G]TCTGTAAAACAGAGA | 90293 |
rs768572899 | snp | A/G | 0.089378 | 0.191574 | intron-variant | KLHL13 | GRCh38.p7 | X:118009563 | ATCAGATAGTTGTAG[A/G]TATGCGGCGTTATTT | 90293 |
rs768582403 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060978 | AGGACACCAGTTACA[C/T]TGAATTAGAGTCTAC | 90293 |
rs768589125 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080734 | TAAAACAGAGTTACC[A/G]TTTGATTCAGCAATC | 90293 |
rs768651367 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099725 | TGGTGGGGGATTCCT[G/T]AAGCCCTGGAGGCAG | 90293 |
rs768666651 | snp | C/T | 2.29579e-05 | 0.00338798 | intron-variant | KLHL13 | GRCh38.p7 | X:117920207 | TTCATATTGTTTTAA[C/T]GTGGTTTCAGAGTTT | 90293 |
rs768668486 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107527 | ATTTAGCCACAAATC[A/T]ATGAAAATAATAATA | 90293 |
rs768674718 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970320 | AAGATCTTATATCAC[A/C]TATGAAGAATTCTAT | 90293 |
rs768676822 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002111 | TGCATCTATAAACAA[C/G]ACAATAATTATTCAG | 90293 |
rs768724381 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099417 | AAGTAAGTATTAATA[G/T]GTGTCTGAAGCTATA | 90293 |
rs768746458 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:117963980 | TCTCACTCATAGGTG[A/G]GAATTGAACAATGAG | 90293 |
rs768749625 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994890 | GTGAGACTTCATCTG[C/T]ATAAAAAATAAAAAA | 90293 |
rs768762078 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052190 | ATATGTTTCAGATAG[A/G]TTAAATATTGCAATA | 90293 |
rs768776068 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118091987 | CATCATGTATTCTCA[C/T]TCATATGCGGGAGCT | 90293 |
rs768787818 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117948983 | AGCCTAAGCCATTGT[C/T]ATATGTTAACAAAGG | 90293 |
rs768789821 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994234 | CTCCCTCCCCCTCTT[C/T]CTTCTTTCCTTCTTC | 90293 |
rs768798815 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018488 | ATAGCAGACAATGTA[C/T]TAATAATGGAGATAC | 90293 |
rs768805096 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118019794 | GTTTGTCAAAGATCA[C/G]ATAGTTGTAGATATG | 90293 |
rs768819204 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965001 | ATTGATGGACATTTG[A/G]GTTGGTTTCAAGTCT | 90293 |
rs768835131 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925326 | CTAGTTTTGATCATT[A/G]TCATTTTAAGTAGAG | 90293 |
rs768835164 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006305 | GTATTTTACCAAAGA[A/C]GGGTTTTATTTTGCA | 90293 |
rs768849280 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117910903 | GAACCATCTCCCCAC[C/T]ATAGAGCAAAATATA | 90293 |
rs768851049 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092885 | CAGGACCTCTCTGTA[C/G]TATCTTTGCAAGTTC | 90293 |
rs768854070 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942787 | TCTATCCAATTTGCC[A/G]GTCTGTGTCTTTTAA | 90293 |
rs768855143 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902833 | GCAGACACTGCCAAC[G/T]GCTAATCCAATTTCT | 90293 |
rs768861377 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118035826 | TTGCAGACGACATGA[C/T]TGTATATCTAGAAAA | 90293 |
rs768864150 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902852 | AATCCAATTTCTTGC[A/G]TCCCCCAACCCTACT | 90293 |
rs768884542 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048284 | AAATGTAAACTGAAG[A/G]AGTAAACAAGTACAC | 90293 |
rs768893937 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040000 | AAACAACCAAGGCAG[C/T]ATCTCCAAGAGTTTG | 90293 |
rs768953002 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118055462 | TTTAAAACAGATATA[C/G]AATATAAAGACACTT | 90293 |
rs768978857 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118093947 | AGCTCCCAACGTGAG[C/T]GACACAGAAGACGGG | 90293 |
rs768983305 | snp | C/G/T | 0.00475684 | 0.0485365 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031456 | TTAGATATATATATA[C/G/T]ATATATATATTTAGA | 90293 |
rs768985033 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014026 | CCACTATTGTACAAA[C/T]TGATTGTAAAATATG | 90293 |
rs768995286 | snp | C/T | 5.44774e-05 | 0.00521878 | intron-variant | KLHL13 | GRCh38.p7 | X:117919750 | TCAATTAAATGAAGG[C/T]GGATAATTATGGTCA | 90293 |
rs769005903 | in-del | -/GAAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099895 | AAGGAAGGAAGGAAA[-/GAAG]GAAGGAAAGAAGGAA | 90293 |
rs769019727 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112636 | AAGGACATATGGGAA[A/G]GTAGGCTGGGATCAA | 90293 |
rs769022045 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017625 | AGACCCGGTGTATAT[A/T]TGTGTTATACACAGT | 90293 |
rs769049321 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118058481 | AAATCCATGGCTAGC[A/G]TCTTGATCTTTCAAA | 90293 |
rs769053017 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104098 | ATGGTGATGTGCGCC[C/T]GTGTTCCCAGCTACT | 90293 |
rs769059266 | in-del | -/AATAGGACCTGGAATTTGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112460 | AATGGGGAATAGTGT[-/AATAGGACCTGGAATTTGA]AATGACAAAAAAGAA | 90293 |
rs769074304 | snp | C/T | 2.28024e-05 | 0.00337649 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909692 | TGACTGCATAACTGG[C/T]TGCATATATGGCATC | 90293 |
rs769076126 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079205 | GAAATGTGAATATCC[A/G]AGAAGCGTAAGAAAA | 90293 |
rs769079579 | in-del | -/TATTCCCTTCATA | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118023557 | TAGTCAAAAAGAGTT[-/TATTCCCTTCATA]TATTCCATTTTTCTT | 90293 |
rs769079739 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118031871 | GTCAGTGGGTGCAGG[A/C]CAGTGGCTGCGTGCA | 90293 |
rs769086185 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118007114 | CAAGTTTGAGAAGTC[A/C]AAAGTAGGAGTCAGC | 90293 |
rs769088116 | snp | A/G | 2.2887e-05 | 0.00338274 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909887 | AAGCCAACGACAGGT[A/G]GCCTTAAAGAGCTCA | 90293 |
rs769095137 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118000430 | GCAATGTATTTCCTT[A/G]CAAACAAAATAGAGA | 90293 |
rs769104999 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072438 | AGGACTTCATGTCTA[C/G]AACACCAAAAGCAAT | 90293 |
rs769106176 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117948629 | GGAGAGACTATATTA[A/C]CGAATTTTGTTTCTA | 90293 |
rs769116525 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907694 | GCTTTTAAAAGTCCA[A/G]TTATTAAAATATATT | 90293 |
rs769117303 | snp | C/G | 0.0194105 | 0.0965841 | intron-variant | KLHL13 | GRCh38.p7 | X:118090744 | AGGGATCTAGAACTA[C/G]AAATACCATTTGACC | 90293 |
rs769117966 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915374 | TCTCTTGTCTCCTTC[A/C]CACTTATGTACCTCC | 90293 |
rs769119773 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104986 | AAACAGAGCTCTGAT[C/T]AGCTGTCAGTAAAAA | 90293 |
rs769137173 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048733 | GACAGAACAAAAATA[C/T]AACGAGACAAGTATT | 90293 |
rs769138801 | snp | A/G | 0.00079164 | 0.0198795 | stop-gained, intron-variant, missense | KLHL13 | GRCh38.p7 | X:118028425 | TTCCATAAATATACC[A/G]GTTACGAAGTATTGC | 90293 |
rs769143934 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018359 | ATCATGCTTTTGCAC[A/G]TGACAATGTTTAGTT | 90293 |
rs769147529 | snp | C/T | 2.2893e-05 | 0.00338319 | missense | KLHL13 | GRCh38.p7 | X:117909508 | AGAGAAAATTTCCAA[C/T]GACGGCGATGCCATG | 90293 |
rs769163830 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118071269 | TCCTTTGGGTATATA[C/G]CCAGTAATGGGATGG | 90293 |
rs769166221 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962135 | AGGATCACTTGAGTC[C/T]GGTGGTCGAGGCTGC | 90293 |
rs769174827 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941058 | CAGCTTTTGCCCATT[C/T]GGTATAATATTGGCT | 90293 |
rs769198800 | in-del | -/TG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081940 | TGAATAGTATTCCAT[-/TG]TGTGTGTGTGTGTGT | 90293 |
rs769209229 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118083271 | GTATCTATCATCATA[C/T]ACCTATGCCCTCGTG | 90293 |
rs769209659 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118106659 | CCTGGTCTTTTCCCT[C/T]CTGTGCACCTGTGGC | 90293 |
rs769213057 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940326 | TGGTACCAGTACCAT[G/T]CTGTTTTGGTTACTG | 90293 |
rs769223002 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018007 | TGTCCTCCTAGACAT[C/T]ACCATAATGCATGCA | 90293 |
rs769235807 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118011940 | TTGGATAAGAAAAAT[A/T]TAGATAAATATTTGA | 90293 |
rs769249129 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117908325 | AGTATACACGTGCCA[C/T]GGTGGTTTGCTGCAC | 90293 |
rs769250006 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118066950 | TATTCTTCCCATTGG[A/T]ATATACATAGAGAGT | 90293 |
rs769256071 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979592 | TGAAAATCAGAATTA[C/T]ATATTGAAGCCAGAA | 90293 |
rs769281614 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000795 | TTAGTATAAATATTC[A/T]TATATTTCACTGCAG | 90293 |
rs769304254 | snp | C/G | 2.28553e-05 | 0.0033804 | intron-variant | KLHL13 | GRCh38.p7 | X:117920229 | TCAGAGTTTTAAAAG[C/G]CAAACTACCTGTGAA | 90293 |
rs769308150 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040515 | ATTTGAAAATAGAGA[A/G]ACAAAAGAAAAAATA | 90293 |
rs769332213 | in-del | -/TTC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943523 | GGAGGCTTTGTTCGT[-/TTC]TTTTCATTCTTTTTT | 90293 |
rs769338487 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118002893 | CATCAAATACTCTTT[G/T]TCTTCCTCATTGTTT | 90293 |
rs769353064 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969155 | CTCACAGGGTCTGTC[A/T]TGCTAGAATTCACTG | 90293 |
rs769364414 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907056 | TAGGAATACCCTAAG[A/C]AAAGCATGATTTCCT | 90293 |
rs769389326 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084278 | TGCTATGATTGCACC[C/T]TTGCACTCCAGCCTG | 90293 |
rs769393947 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041296 | CTTTGGGGGACCAAG[A/G]TGGGTGGATCACTTG | 90293 |
rs769394020 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | KLHL13 | GRCh38.p7 | X:118033118 | ATCTGCGTCTGACTG[A/G]TGTACCTGAAAGTGA | 90293 |
rs769400792 | in-del | -/GGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117956721 | GAAGCAGACAAAAGG[-/GGA]GAAGAGTCACCATGT | 90293 |
rs769407277 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044039 | GATAAATTCAGTAAA[G/T]CTGCAGGATACAAAA | 90293 |
rs769430314 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029674 | CAATTTAGTTTATTC[A/T]TAAAGTTATGTTGGC | 90293 |
rs769433178 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030976 | CCTGGATTTCTGAGT[A/C]TGGGATATTCTTATT | 90293 |
rs769441899 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065409 | CCACAAGGCAAACAT[A/G]GGTTGTTCTTTCCAA | 90293 |
rs769453720 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944630 | ATATGCATTTAGAAA[G/T]GCAAATTTTCCTTAT | 90293 |
rs769454709 | snp | C/G/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974796 | GTAATATATGAACTT[C/G/T]GTAAATATTAAAATT | 90293 |
rs769479565 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118835 | ATTTATGTGCTATGT[C/G]ACATTAAGTTAGTGC | 90293 |
rs769482890 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118012668 | GATTAAAATGTGGCC[A/C]TCCTGGGCGGGGGCG | 90293 |
rs769483912 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033354 | AGAGAAAGGTCGGGT[C/T]ACCCTCAAAGGGAAG | 90293 |
rs769492739 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118064805 | TTTCTGTGTGTTTTA[A/G]TTTCTTCACTGCTTC | 90293 |
rs769496926 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928942 | AAAACTCTAACAAGA[C/T]GGATTAGGTGAGAAA | 90293 |
rs769509987 | snp | A/C | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118095206 | GGAAGATCTACCAAG[A/C]AAATGGAAAACAAAA | 90293 |
rs769520141 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021877 | AAAGTGTTCCTATTT[A/C]TCCACATCCTCTCCA | 90293 |
rs769522827 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083719 | AGAAGAGAGGATTTC[A/C]AATGTTCTCACCGTG | 90293 |
rs769531833 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118045254 | TGGCAGGCGCCTGTA[A/G]TCTCAGTTACTAGGG | 90293 |
rs769535697 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013988 | GTTATCTTCGTAAGC[A/G]GAGAATGTATGTCAC | 90293 |
rs769559439 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118037831 | CTAGAGATCAGTTAA[C/G]AAAGTTCTTCTACAG | 90293 |
rs769565804 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118003787 | AAGGTGGCAACAACT[C/T]GTCAAAGTACAGAAA | 90293 |
rs769569140 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045732 | GAATTGCTTGAACCC[A/G]GGAGGCAGAGATTGC | 90293 |
rs769584487 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:118071418 | TCCTCTCCAGCATCT[A/G]TTGTTTCCTGACTTT | 90293 |
rs769588169 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045264 | CTGTAGTCTCAGTTA[A/C]TAGGGAGGCTGAGGC | 90293 |
rs769606195 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994559 | ACCCAGAAGCCTATT[A/C]TAGCATTTTCTGAAA | 90293 |
rs769609257 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117965625 | ATTTTAGACCAATAT[C/G]CCTGATGAACGTCAA | 90293 |
rs769618306 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118015432 | AAAATAAACAACTTT[C/T]AGTCTGGGACTCAGA | 90293 |
rs769638954 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117927054 | GGGACTATAGGCGCA[C/T]GCCGCCACGCCCGGC | 90293 |
rs769650091 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117913345 | AAATGGATAATTGGA[C/T]TTATAATGCAATTTA | 90293 |
rs769650844 | snp | C/G | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117415 | GAAGGATAAAAACTA[C/G]AAATAACAGTTTAAC | 90293 |
rs769653793 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004433 | GATTCCAGAGCTAAT[G/T]CAGAGAAAGTACAAG | 90293 |
rs769663590 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117979079 | GGGATTACAGGCATG[C/T]GCCACCACGCCCGGC | 90293 |
rs769666079 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954216 | CCTCTGCTTACCATA[C/T]TTCAAGACTTTAGTG | 90293 |
rs769670467 | in-del | -/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987219 | GTAAGTGGAGAGAAA[-/T]TGTGATTGTGCTTTA | 90293 |
rs769684290 | in-del | -/CA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069111 | CATCCAGAAGAGTCA[-/CA]CACACACACACACAC | 90293 |
rs769692220 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117918624 | CCCAGAAGTAAAATT[C/T]AAAGGTCTCAACTAA | 90293 |
rs769693337 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904466 | CTTCAATCGTAGTCT[A/G]TAAGAGTTGGAAATG | 90293 |
rs769699386 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118079204 | AGAAATGTGAATATC[C/T]GAGAAGCGTAAGAAA | 90293 |
rs769708132 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118016124 | AGCATGTACTATGTG[C/T]TTCGTCTTAAAAATA | 90293 |
rs769710898 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967958 | AAAAAATAATATAAT[C/G]TCAGGCCCTTTAAGA | 90293 |
rs769714222 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118114960 | TGCCATAAGACGTGC[C/T]ACCAGGACAGTGAAA | 90293 |
rs769718175 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997169 | CGTAACCACCTCTAA[C/T]TTAAATAGTATGCTA | 90293 |
rs769748288 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024381 | CAAAAAGCACCAAGC[A/G]TAACAGAAGAAAAAT | 90293 |
rs769749654 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118095780 | ACTGAACAACCTGCT[A/C]CTGAATTACTACTGG | 90293 |
rs769762374 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118061713 | AAATGGCAGAGGATA[C/T]TTGAGTCCATTCTTA | 90293 |
rs769775359 | in-del | -/GAAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930217 | AAGGATGAAAAGGAA[-/GAAG]GAAGGAAGGAAGGAA | 90293 |
rs769785392 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080652 | AGGGAACACTTATAC[A/T]CTGTTGGTGGGAATG | 90293 |
rs769787503 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089109 | CTAAACACTACAGAA[A/T]AAAATATGGCTGCAC | 90293 |
rs769798466 | snp | A/G | 2.28141e-05 | 0.00337736 | missense | KLHL13 | GRCh38.p7 | X:117899191 | CACTGGTCAAGGATA[A/G]GTGAATAGTATTCAC | 90293 |
rs769799588 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118008793 | CCATGCTTATTTACT[C/G]TGTGGCCTTAGACAA | 90293 |
rs769802137 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070247 | TGTGTAAGCATTTAA[A/G]GCTACAAATTTTCCT | 90293 |
rs769805361 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118106331 | ACAGGAATAAACAGA[A/T]TAAGAACAGTTAATC | 90293 |
rs769823157 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118060638 | AAACAGAGGCTTCTC[A/T]GAGTTTATTAATATG | 90293 |
rs769836056 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118051992 | TATTACAGTGTGGTA[A/C]TAGTGTGGGAACAGA | 90293 |
rs769842309 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900379 | TATAGTTTCTAACCA[C/T]TCTTGATTGGGAAGG | 90293 |
rs769843172 | snp | C/G | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972894 | TACCAACTAAGACTT[C/G]CATTCCACACTGTAC | 90293 |
rs769865195 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117959466 | AGAAGAGCTCTGATA[C/T]AATCACATTTAATAA | 90293 |
rs769875152 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118081273 | CCCTAACAAGAATAA[A/C]TTATTTTTCTATCAA | 90293 |
rs769881780 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118032219 | AGCAGCCAGGAAGCT[C/T]GAACTGGTTGGAGCC | 90293 |
rs769885208 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118009307 | TGCTTTTGGTGTTTT[A/G]GACATGAAGTCCTTG | 90293 |
rs769887447 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117970496 | ATGTTTGCCAGCCAA[A/G]CAATTGTGAGAACAA | 90293 |
rs769892652 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032419 | AGACTGCCTCTTCAA[A/G]TGGGTCCCTGACCCC | 90293 |
rs769896073 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974285 | CTAAAAACAGAATTA[C/T]CCATTTCCATCAATG | 90293 |
rs769896134 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951289 | ATTTCAAATATTGAA[A/G]GATTTGTCCCCCAAC | 90293 |
rs769897255 | snp | A/G | 5.08511e-05 | 0.00504212 | missense | KLHL13 | GRCh38.p7 | X:117910089 | TCAACACAGTTGTCT[A/G]AAGTGACCTATTAAG | 90293 |
rs769901796 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088350 | TAATCATTACTTAAG[C/T]ATTATATATAATACA | 90293 |
rs769905162 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001915 | TCATCGTGTTGCATA[A/T]GAATCTTACAGATTT | 90293 |
rs769917450 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942761 | TGAATACAGCACACC[A/G]ATGGGCCTTGTCTAT | 90293 |
rs769933395 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968720 | TAATCACAAATGATT[A/G]TCAATTTAATAAGTA | 90293 |
rs769937284 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039872 | ACCTCTCCCTCAGCT[A/C]TAAACAACTCAGAAA | 90293 |
rs769938227 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117971162 | CCATCTCTAAAAATC[A/G]ACAAATCAGGGGCAA | 90293 |
rs769939778 | in-del | -/AAATA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117979919 | TAAACTACTTTGAGT[-/AAATA]AAATAGTCAAGCTAT | 90293 |
rs769956850 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118066753 | CTGATGAAAGATTTA[C/T]ATCCAGAATCAATAA | 90293 |
rs769961072 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117994055 | GCATTTATTAAGTAA[C/T]TTTTCTCCCTGTTTC | 90293 |
rs769965733 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951008 | AGAAGCCATTTTCCA[C/T]TGGCTTTTTAAGATA | 90293 |
rs769971086 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938345 | TAAAATATATAGGGA[C/G]AAAAGAAAAGGCCAT | 90293 |
rs769973770 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118025595 | GGTGACTTGGATATA[C/T]CAAAGAGAAGCCATA | 90293 |
rs769982540 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111495 | GGGGGAGGTGGTTCA[C/T]GCCTGCAATCCCAGC | 90293 |
rs769985286 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117953733 | CAGACAGTAGAGGCT[A/G]TAAGTCACTTAGCAT | 90293 |
rs769989210 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005943 | AGGCAGGAGAGTGAA[C/G]TGTAACTGAATTAAC | 90293 |
rs769994506 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944960 | CTACCAATGCGAGTT[C/G]GGACACCAAATAAAT | 90293 |
rs770012175 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000726 | TATGAACTCATCTGG[C/T]AGTCAAGCTTGACCT | 90293 |
rs770018265 | snp | G/T | 0.000179888 | 0.00948219 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973418 | CGCTAATAGAGATCA[G/T]TGACTAAATTCAGCA | 90293 |
rs770022455 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117955775 | ACCATTAAGGGTTTT[A/T]TTCCACAAAACTTTA | 90293 |
rs770037210 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118098305 | AAGACATTTATGCAG[C/T]CAAAGGACACATGAA | 90293 |
rs770043777 | snp | C/G | | | utr-variant-5-prime, intron-variant | KLHL13 | GRCh38.p7 | X:117985385 | GTAGCGCACCCCAGT[C/G]CATCTGCCTGGTACA | 90293 |
rs770046512 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117934579 | AGAACAAGAAGGGAC[C/T]ATAAAGCTGAAGGTG | 90293 |
rs770052015 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117993216 | TAGGAGAGAGGGTGC[A/G]GGTGCAAGACTAGTT | 90293 |
rs770052454 | in-del | -/TG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081941 | TGAATAGTATTCCAT[-/TG]TGTGTGTGTGTGTGT | 90293 |
rs770057263 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | KLHL13 | GRCh38.p7 | X:117963963 | AACCAAACACCGCAT[A/G]TTCTCACTCATAGGT | 90293 |
rs770064324 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117933699 | AGCAAAGTAGCATCT[C/G]TTTTAATGATAACTA | 90293 |
rs770096979 | snp | C/G | 0.000137898 | 0.0083024 | intron-variant | KLHL13 | GRCh38.p7 | X:117919503 | CCACAGGAAAAATCA[C/G]ATTTCAAAATATCTT | 90293 |
rs770112490 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118035639 | ACAGCCAATATCATA[A/C]TGAATGGGCAAAAAC | 90293 |
rs770112496 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117964435 | TTAATTGCTTATGAA[C/T]GAAGATAGTATGGAA | 90293 |
rs770117263 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117918575 | ACCTCTGGAAGTCTT[A/G]GCAATATTTCTGTCC | 90293 |
rs770119885 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118058128 | TTTAAAGCCTCTCCA[C/T]TACATAGTGTTACCA | 90293 |
rs770132101 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092422 | AAGTGCTGAAAGATA[A/G]GAACTGTCAACTCAG | 90293 |
rs770145766 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947137 | ATGATATATAGCACA[A/C]ACACACAATTTTAAA | 90293 |
rs770155423 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979092 | TGCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 90293 |
rs770175311 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038969 | TAGCTTACCTACAGT[A/G]GGCTAGGACAGCAGG | 90293 |
rs770186746 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118067285 | GATAAAAAATGGTAC[A/T]CCTGTATAGGGCACT | 90293 |
rs770189735 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117924785 | AATATTTCCCTTTCT[G/T]CTTCTATAAATCTCC | 90293 |
rs770194139 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118005630 | GATTTGACCCAGCAC[C/T]GCTGGCTTCGAAGAT | 90293 |
rs770220157 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093117 | ATTTGCCTGCTAAAA[A/G]TGCCTCCACTAGTTG | 90293 |
rs770232271 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117900473 | CTCAGAGGAGTTGGA[C/G]CTCTCATTATAATGG | 90293 |
rs770235096 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070205 | TGCATTTCTCAGAAT[A/G]TATACCTGTCGTTAA | 90293 |
rs770237236 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118091646 | CAGAATTAGGGACTT[C/T]AGGGACTATAACAAA | 90293 |
rs770245936 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118013879 | ACTGCAATCTCTGAA[C/T]ATAAATTGTGAAGAT | 90293 |
rs770248834 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928978 | AGAATATACAAATTA[C/T]CAATGCCAGGATGAA | 90293 |
rs770249268 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907222 | TAGATGGGTATACCA[A/T]AGGAGCAGCTGAAAG | 90293 |
rs770257918 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079181 | TGAAATTGTAAATTC[A/G]CAGAAAAAGAAATGT | 90293 |
rs770273143 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056794 | TTCATCTCATTAATT[C/T]TCAGAATGTTACTAG | 90293 |
rs770278051 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118103244 | AAAGGTATGCATAGA[-/T]TTTTTTATTCTAGTG | 90293 |
rs770292102 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073536 | TCATCCTCTCTACAT[A/C]TACTTGGCTGTGGAT | 90293 |
rs770317467 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039603 | ATTCCTAAGGTTTCC[A/G]ACTCTAGGCTTTAAC | 90293 |
rs770317756 | snp | C/G | 2.2969e-05 | 0.0033888 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972771 | ACCTGGATGTTTTAA[C/G]CACAGGAACTGGGAA | 90293 |
rs770323243 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968042 | TGGAGCATCACATTC[-/A]AATGTAGTGTCTTAC | 90293 |
rs770330003 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006224 | TGGTGGTAAAGGCTA[C/T]ACTAATTTAACTATA | 90293 |
rs770336726 | snp | A/G | 9.16275e-05 | 0.00676797 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909482 | ATAATTACTCTGTCC[A/G]CCAACCACATAGAGA | 90293 |
rs770361322 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118057543 | ATGTGAAAAATCGGC[C/T]GGGGCCGTGGCTCAT | 90293 |
rs770369304 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117975949 | AAACAATCAACTGAT[C/T]CAAAAAAAACAACAT | 90293 |
rs770369854 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117916182 | AAACAAACAAACAAA[A/C]AAAAAAACACTAGCT | 90293 |
rs770372121 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118104032 | CCTGGGCAACATACC[A/G]AGGCCTCATTTCCAC | 90293 |
rs770403464 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117946703 | TCTTCATTTTTTCTG[C/T]AATTTCCTCAATTTT | 90293 |
rs770415688 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117906568 | AAACCTCTTGCTTCT[C/T]GGCTTTATCTAATGA | 90293 |
rs770462541 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028685 | TTAAAAAACTGAAAG[C/T]AAAAATATCTATGAA | 90293 |
rs770474423 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117981062 | ACAAACAGCTAAAGA[A/G]TACAGAGACAGTTAT | 90293 |
rs770481207 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000119 | TACAAATGCCAAAGA[-/T]TTAATCAGTTAACCT | 90293 |
rs770493844 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977221 | TAGAAGTGGGAGAAA[A/G]ACACCATAAAAGAAA | 90293 |
rs770496093 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011497 | AAAAAAAACAGATTA[A/G]AAGGATATTTTAATG | 90293 |
rs770501467 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922211 | TGTTTTTTTGAGACA[C/G]AGTCTCGCTCTGTCG | 90293 |
rs770509751 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118096818 | TATAAACAGAACCAA[C/T]GACAAAAACCACATG | 90293 |
rs770517252 | snp | G/T | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:118071967 | CTTTCTTCACAGAAT[G/T]GGAAAAAACTACTTT | 90293 |
rs770523777 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117920547 | ATGTGACAATGCATG[C/T]TTTCTTTCACTGTAG | 90293 |
rs770530410 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118116444 | GCCGCGCACCGCGCA[A/G]CGCCGGGTCCGAAGG | 90293 |
rs770540432 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118062431 | TTTTCATTTTCTGTA[A/G]TTTTCTATACAGAAT | 90293 |
rs770547323 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117939504 | GTTCTAGATCCTTGA[A/T]GAATCACCACACTGT | 90293 |
rs770552864 | snp | C/T | 3.03053e-05 | 0.00389252 | intron-variant | KLHL13 | GRCh38.p7 | X:117909254 | TGATTTGATAAGAAT[C/T]TCTGAGTGAAGAAAT | 90293 |
rs770557053 | in-del | -/TCT | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118040346 | CTGTTTTGATGAACC[-/TCT]TCAATGAAATTAAAG | 90293 |
rs770557430 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048658 | ATGTAGATGTGCAGA[C/T]GGGATATGACATAGA | 90293 |
rs770558082 | in-del | -/TAAACA | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:117991419 | ATCCCAAGCCAAGAG[-/TAAACA]TAATACTCCATCATT | 90293 |
rs770580180 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117952611 | CTACCATCAGAATGA[A/G]CAGGCAACCTACAAA | 90293 |
rs770582762 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108454 | CCTTTTTCTTCTTCA[C/T]CTTTCTCATCTGGAG | 90293 |
rs770586362 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970710 | AAATGGTCAAAAACT[-/A]AAACAACATATTTAA | 90293 |
rs770589729 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050982 | ATGTTGCTGCTGCAG[G/T]ATCATAAATGATTGT | 90293 |
rs770591608 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118090572 | GCAAATCAAAACCAC[A/T]ATGAGATACCATCTC | 90293 |
rs770607087 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064420 | GCATTAAGGTTTAGA[A/G]TATAAGGTTAAAAAA | 90293 |
rs770610350 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118017960 | TCAGAAAATACCGCC[A/C]CAACAACAAACTGGT | 90293 |
rs770617458 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093373 | TCTATAAAATCTCTT[G/T]TTCCTCCATTAGAGA | 90293 |
rs770618489 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117929916 | GCAGTGAGCCAAAAT[C/G]ATGCAACTGCACTCC | 90293 |
rs770630404 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962071 | TAATAATAAGCTGGG[C/T]GTGGTGATGCGTGCC | 90293 |
rs770630418 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082525 | TTGTCAGATGCACAG[G/T]TTGAAAATATTCTCT | 90293 |
rs770631951 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118053384 | TCTCAGCAAACTATT[A/G]CAAGGACAAAAAACC | 90293 |
rs770637050 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914988 | TCAGAATGGATGGCC[A/G]ACCATAAGCAACGGG | 90293 |
rs770648616 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118033082 | GCCTCCAAGAAATGT[A/G]GGACTATGTGAAAAG | 90293 |
rs770658007 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045024 | GTGATTAATAACCAA[A/C]ATATGTAAGGAGCTC | 90293 |
rs770660975 | in-del | -/AAAAGGGTG | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117981794 | ATAACATGTATTCCA[-/AAAAGGGTG]AAGAGGCAAGATCGA | 90293 |
rs770668854 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118100770 | TCTCAAAATTCTCCC[A/C/G]TATATCCTTGTCTTT | 90293 |
rs770669353 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118052787 | AGCCAAGATCGTACC[A/T]CTGCACGCCAGTCAG | 90293 |
rs770689811 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117921533 | GAAATGTTTCATTAT[A/T]AAAAACCAGGAAGAC | 90293 |
rs770692573 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118028203 | ATTTATACCAATTAC[A/T]TTTTCTAAATATATT | 90293 |
rs770698496 | snp | A/G | 0.00016218 | 0.00900353 | intron-variant, missense, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973365 | TTGAGCTGCAACAAT[A/G]CAAATGGGATATAAA | 90293 |
rs770709608 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973674 | CACATTTACAACATG[C/T]TGTAGTAACACAAAT | 90293 |
rs770710564 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117668 | AACTGCTTCCAAACT[C/T]TGGTGGGACTGCTCT | 90293 |
rs770719665 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118045031 | ATAACCAAAATATGT[-/A]AGGAGCTCAGCAACT | 90293 |
rs770730936 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118106420 | GCTAATGACCTAATG[A/G]TAGAGTAAGTCTAAT | 90293 |
rs770733153 | snp | C/T | 4.58206e-05 | 0.00478625 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909449 | GACTGTATCAACTGC[C/T]GTTTTTCCTTTTGTA | 90293 |
rs770736453 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113367 | CCTTCCCCAGGAAAG[A/T]CTCTTCAGTGGCTTC | 90293 |
rs770738585 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114753 | TTGATAAGCAATAGG[C/T]CTTACTTTTCTTGTG | 90293 |
rs770742495 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912950 | CTGTTGAATTAATGT[A/G]GCAAATTACTAAAAC | 90293 |
rs770758837 | snp | C/T | 4.56366e-05 | 0.00477663 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117919569 | AACTGGCAGAATCTG[C/T]AGGAAACTGGCAGCT | 90293 |
rs770769104 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117996100 | GGTGGACTTTGTATA[A/G]CACACTTTGTGTTTC | 90293 |
rs770771885 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118083182 | CCAATATAGACAACT[A/G]TATGGAGGTTCCTCA | 90293 |
rs770780661 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029041 | AAAACATAGTATATA[C/T]AGGGTTCGGTACTCT | 90293 |
rs770780849 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020899 | CACAAGGACAGAAAA[C/T]CAAACACCGCATATT | 90293 |
rs770783181 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963914 | GGATGAAATTGGAAA[C/T]CATCATTCTCAGTAA | 90293 |
rs770784659 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100550 | TTTTAAATTGGCACA[-/A]TTAGACAATATGCCA | 90293 |
rs770789528 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014612 | TTTTAGAATCCCTAA[A/C]AAAAACTTGCTGGTT | 90293 |
rs770799644 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117937347 | ACCACAGGAAATATT[C/G]TAACAACATAAAAAA | 90293 |
rs770814589 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912092 | TTGTAAATGGAGTTA[C/T]AGTCAATACCTGTTT | 90293 |
rs770823636 | snp | C/G | 0.0655152 | 0.168717 | intron-variant | KLHL13 | GRCh38.p7 | X:117903161 | ACACACACACACAGA[C/G]AGAGAGAGAGAGGAG | 90293 |
rs770825042 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906744 | AAGGGACGCAATCAT[C/T]TTCTACAAAAGTTTA | 90293 |
rs770838054 | snp | C/T | 0.0850455 | 0.187856 | intron-variant | KLHL13 | GRCh38.p7 | X:118094490 | TATCCAGGAGAACTT[C/T]CCCAATCTAGCAAGG | 90293 |
rs770859762 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083776 | TGATATCCTAATTAC[C/T]CTGATTTGATCATTA | 90293 |
rs770861859 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075835 | TATTCTAACTGAAGG[C/T]TGGGTATGCTTTACC | 90293 |
rs770873007 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117984799 | TTGCTTTAAAATGCA[C/T]CAAAATGTCTTTAAA | 90293 |
rs770876714 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118067519 | CTTTTAAATTTTTTT[-/T]AACTTTTTGCCTCTT | 90293 |
rs770878144 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908721 | GATGGGCTTATGGAA[A/G]AGAAAACTATCTGAT | 90293 |
rs770885881 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118101569 | TTCCTAGAAGAGGTG[C/G]TATCTAAACTGAAAC | 90293 |
rs770900697 | snp | C/G | 2.33446e-05 | 0.00341639 | missense | KLHL13 | GRCh38.p7 | X:117898961 | GTGTGGTTTCTTCTG[C/G]TGGAAAAACTGTGAG | 90293 |
rs770903242 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987211 | ATAGAGCTGTAAGTG[A/G]AGAGAAATTGTGATT | 90293 |
rs770921237 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965070 | CATGTGTCTTTATAG[C/G]AGCATAAATTATAAT | 90293 |
rs770927684 | snp | G/T | 0.0317957 | 0.122012 | intron-variant | KLHL13 | GRCh38.p7 | X:118095054 | AATATTAACCTTAAA[G/T]GTAAATGGGCTAAAT | 90293 |
rs770935052 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045661 | TACACACAAAAAAAG[G/T]AGATGGGCGTGGTGG | 90293 |
rs770946486 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904360 | TTTCCATATTTACAC[A/G]ACACTCAGATATAGG | 90293 |
rs770948659 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117898051 | TCAAAATTTCTAGCC[C/T]TTATCCACCTAAATT | 90293 |
rs770949217 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118069497 | AAGACTTCACCATTA[C/T]ACAATATACCCATGT | 90293 |
rs770949341 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117996922 | CAAAAAGATAAAGTA[C/T]GGATTCATCACAAAA | 90293 |
rs770963298 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092546 | CCTACCCTATTAGTT[-/A]AAAAGAAGTTATCTA | 90293 |
rs770977548 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117901509 | CTCCGTTTTTCTGGA[-/T]TTTTTTTTTTTTTGA | 90293 |
rs770980788 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117936699 | AGGAACCACATCCCA[C/T]AGCCAGAGCCTGGTC | 90293 |
rs770995576 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060533 | ATAGAATTCTTCCAC[A/G]TACCAGACACTTTAC | 90293 |
rs771017646 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088237 | TACTGTTTCAAAGAA[C/T]GTAAAACAATACCCT | 90293 |
rs771024643 | in-del | -/CT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080565 | CCACAATGAGATACC[-/CT]CTTACACCAGTGAGA | 90293 |
rs771025547 | snp | A/C | 0.11443 | 0.21005 | intron-variant | KLHL13 | GRCh38.p7 | X:118036728 | CAATGGCAACAAAAG[A/C]CAAAATTGACAAATG | 90293 |
rs771031709 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117992330 | GAATCCATCGCACCT[C/T]TCCTGACTCTCTGCT | 90293 |
rs771033960 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917952 | ATCACATTCAATATG[A/C]TTCATTTTTCCTTGA | 90293 |
rs771047770 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117957391 | TCACCCTCCTTAACT[A/C]ATTGCACAGTCCAGC | 90293 |
rs771053021 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118097625 | CCGCATTGCCAAGTC[A/G]ATTCCAAGCCAAAAG | 90293 |
rs771055252 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118008696 | GTCCTCAGGGAGTTT[A/G]CATTCCAGGGAAGGA | 90293 |
rs771059081 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950871 | ATTTCTTGTGATAAA[A/C/G]TTGCATGGCAGGTGG | 90293 |
rs771061693 | snp | C/T | 2.45577e-05 | 0.00350403 | missense | KLHL13 | GRCh38.p7 | X:117910050 | ACTTCGGTTAGATTG[C/T]AGGTGTTGGCAATCC | 90293 |
rs771075194 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050146 | CTGTCTCGGCCTCCC[A/G]AAGTGTTGGGATTAT | 90293 |
rs771091113 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113035 | TAAGATATCATTCTT[C/T]GAAAAATAAATTCTT | 90293 |
rs771100899 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117958412 | CACCTATTTTCATGC[C/T]ATGGTTAACCATGGG | 90293 |
rs771104372 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005000 | TCAAGAGAAGACTGA[C/G]AAAGTGTTCCAGATA | 90293 |
rs771114561 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118073107 | TCAAAAAAAAAAAAA[A/C]CCCACAAATGAAGAA | 90293 |
rs771130509 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117970410 | ACGATTTATTGAGGA[A/G]TCAGAATTGAACAAT | 90293 |
rs771135368 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117950139 | TTAAATCTAACAATA[G/T]ATGCTAAAAACTCAA | 90293 |
rs771140490 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024163 | GCCATTTACAAAGGT[A/G]TTAGCTTAGAATTAA | 90293 |
rs771153255 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019084 | AAAATCTACTTCCTT[A/G]GAAAATTTTCAGAAT | 90293 |
rs771182782 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113692 | CTTCCCACACTAAAG[G/T]AGGCCCTTCCTAGCT | 90293 |
rs771184017 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941821 | TGAAGTGTTCCTCGT[A/G]TCTCTATCTCCTTCA | 90293 |
rs771184657 | in-del | -/G | 0.00949095 | 0.0682305 | intron-variant | KLHL13 | GRCh38.p7 | X:118104995 | TCTGATTAGCTGTCA[-/G]TAAAAAGATTGTCAA | 90293 |
rs771188271 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941252 | GGATTACATTTTATC[A/G]AGGATTTTTGCATCT | 90293 |
rs771191128 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057741 | TGAGGCAGGAGAATG[A/G]TGTGAACCTGGGAGG | 90293 |
rs771192998 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118032210 | GGTAAACAAAGCAGC[A/C]AGGAAGCTTGAACTG | 90293 |
rs771213777 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935091 | AAAAATTAGACAGAA[C/T]TACCATAGGATCCAG | 90293 |
rs771224768 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117926463 | TCTGCAGAAAGAACC[A/G]CCAAAAAAGAGCACA | 90293 |
rs771227637 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118077374 | CTTAAGGATGGATGA[A/G]GTTTAAATTACTGCC | 90293 |
rs771239675 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081181 | CATGCTACCTGAGTG[C/G]GATATACCCATGTAA | 90293 |
rs771250661 | in-del | -/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118921 | TGCCCCACAGCATTG[-/T]TTTGGGTTTCAAATA | 90293 |
rs771255285 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907741 | TCATGATCATGCGAC[-/AT]AGTCCAACAATCTAG | 90293 |
rs771255341 | snp | A/G | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118053 | TTTGTATTTCAACTT[A/G]CATACACTGAAATTC | 90293 |
rs771265721 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069915 | CAGTCCTGCAAGCTC[A/C]ATTCATGATAAATGC | 90293 |
rs771267126 | in-del | -/TGTTG | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971080 | GTGATTAATTTAAAA[-/TGTTG]TGTTGAGTTGTATCT | 90293 |
rs771278439 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118026131 | ATGGTATCTGTCAAG[C/T]AACAGTAACTTTATA | 90293 |
rs771282854 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078978 | ACATTCTAGTAGGTT[A/C]CTAGGGGTATCTCAT | 90293 |
rs771316686 | in-del | -/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118092929 | TTATTTCAAACAAAC[-/T]TTTTTTTTCTTTTTA | 90293 |
rs771328471 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118012688 | GGGCGGGGGCGGGGG[C/G]AGGGGGCGGGGGTAT | 90293 |
rs771329546 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118073827 | TGCCAGTAACTGTCA[C/T]GTGAGCCTGCCTCTA | 90293 |
rs771345562 | in-del | -/CTTTA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013950 | ATTTCTTATGCCTGT[-/CTTTA]CTTTAATCTCTTAAT | 90293 |
rs771347317 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118035497 | AGACAAAAACCACAT[C/G]ATTATCTCAAAAGAT | 90293 |
rs771354251 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118092346 | GGAAACAATTCACAT[A/G]ACAGCAGATTTTTCA | 90293 |
rs771362866 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117909147 | TGCCCAGATAAGGCA[C/T]AAAGATGGTCTTCAA | 90293 |
rs771368224 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118019520 | CATTTGTCAATTTTG[G/T]CTTTTGTTGCCATTG | 90293 |
rs771369046 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117992235 | GAGAAACTGAGATGT[A/G]AAAAAAAAAAAAAAG | 90293 |
rs771378685 | in-del | -/AGAGA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053840 | GAGAGAGAGAGAGAG[-/AGAGA]GAGAGGAGAGAGAGA | 90293 |
rs771408191 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084486 | GGTTGTGAGGAAACA[A/G]GTACTTAGAGGAATA | 90293 |
rs771413330 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900181 | ATGAAAGTATTAAAC[A/G]ATACCTTCTGTAGAC | 90293 |
rs771418515 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013221 | ATGAGTCTTATGGAG[A/G]GAATTAAATTGGGAT | 90293 |
rs771425799 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | KLHL13 | GRCh38.p7 | X:117963889 | GAGTTCATGTCCTTT[A/G]TAGGGACATGGATGA | 90293 |
rs771428598 | in-del | -/CTC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902314 | AAAAGAAATGAAAAA[-/CTC]CTCAATTCTGGGTCC | 90293 |
rs771432336 | snp | C/T | 2.30651e-05 | 0.00339588 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972753 | CTGGAGAAAGTGGAG[C/T]TGACCTGGATGTTTT | 90293 |
rs771433794 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914229 | AAAATGGGTATCTGC[-/T]TTTTTTTTTTTTTTT | 90293 |
rs771439040 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088194 | TATTGTTAAAGCAGA[C/T]AGCCTTTTCCTCAAT | 90293 |
rs771445940 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117900267 | TGGCCAGATGCCAAT[C/T]ACTATCACTGTTTCC | 90293 |
rs771452254 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117983895 | CAGTAAATATATACT[C/T]GCCCCTTGGAATAAT | 90293 |
rs771478790 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117955594 | TTTTAAGACAGGGGA[A/G]AATAATACAAAAAAA | 90293 |
rs771486983 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118016042 | ATTAATAAAAGGACT[C/T]ATCTCCAATGGCTGA | 90293 |
rs771487343 | snp | C/T | 0.000595436 | 0.0172442 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909905 | CTTAAAGAGCTCAAG[C/T]TCAGTACAGTGCTTA | 90293 |
rs771494356 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998052 | GAAGCCAAAAGCAAT[G/T]CTGGGGTTGGAAACT | 90293 |
rs771498197 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085321 | TTTATATAACATGTC[C/T]AGAATAAGCAAATCC | 90293 |
rs771507091 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975175 | AAAGAAGGAGAAATA[C/T]ATACACACACACACA | 90293 |
rs771522179 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117954657 | TGCACATGTGATAAT[G/T]GTGGTAGGGAGATGG | 90293 |
rs771534683 | in-del | -/CA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069110 | GCCATCCAGAAGAGT[-/CA]CACACACACACACAC | 90293 |
rs771558420 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111384 | TCAGGTTTTGCCACC[A/C]CATGAGTTTTGGCAT | 90293 |
rs771560353 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117956833 | CTCCATGAGATACTT[A/G]TTGAAGCAATCATCA | 90293 |
rs771562092 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911272 | AAATAAAATAATCCT[C/T]CTGTTGACATTTCTT | 90293 |
rs771570385 | in-del | -/TT | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118038932 | AAGGGAAAAAGATGA[-/TT]TTGTCTTGCAACTTG | 90293 |
rs771586159 | in-del | -/TGG | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078201 | TTTCATAATCACAAA[-/TGG]TGGTCCAATTTATAA | 90293 |
rs771596093 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006194 | ATAAGAGGGAAAGTA[-/T]TTTACATACAAAAAT | 90293 |
rs771596130 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117966293 | CAGCCAAATCATGAG[G/T]GAACTCCCATTCACA | 90293 |
rs771601136 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913153 | GTAAACAATGGCCCA[C/G]AGAAATACATAATAT | 90293 |
rs771615535 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938512 | GGTTTGGGACCTAGC[A/G]TTCAGTGTTTTAACA | 90293 |
rs771616236 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056536 | GAAAGCCTTATCTGT[C/T]CTGGGTAAAAAAATA | 90293 |
rs771628517 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967691 | GCTCTTTGTCTTGCA[A/G]GTGTCTTGTGTGCAA | 90293 |
rs771646762 | snp | C/T | 0.000791014 | 0.0198716 | utr-variant-5-prime, intron-variant | KLHL13 | GRCh38.p7 | X:118028494 | CTAAAAGTTGGATAA[C/T]GACCTGTTCAGGAGG | 90293 |
rs771649530 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967289 | CTTGAGGATATAAAG[A/C]AATACATCATGGCAG | 90293 |
rs771659080 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118022097 | GATTTTTTCTTGCAA[A/G]TTTGTTTAAGTTCTT | 90293 |
rs771662154 | snp | A/G | 2.36471e-05 | 0.00343846 | intron-variant, splice-donor-variant | KLHL13 | GRCh38.p7 | X:117972729 | TATTTTCTCTCACTT[A/G]CATGTATGCTGGAGA | 90293 |
rs771696194 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117997613 | AAAGTACGTATTGCA[A/G]GGCTCATTTGTGCCA | 90293 |
rs771701514 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118047888 | AGGGAAACCAGGAAG[G/T]TGTGGTAACCCAGAA | 90293 |
rs771704110 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947058 | TTAAAAAGCATAAAA[G/T]AAACTGGATATAGCC | 90293 |
rs771706107 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118057460 | ATGACACCAAAAGCA[C/T]GAGCAACAATAGATA | 90293 |
rs771742237 | snp | A/C | 2.35278e-05 | 0.00342977 | missense, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117945556 | ATTTCATGTGTTGGT[A/C]TTCCTCTTCCACGAG | 90293 |
rs771746741 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118095961 | TATAGCACTAAATGC[C/G]CAAAAGAGAAAGCAG | 90293 |
rs771746928 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118022729 | TGTAAGTTATGTTAA[G/T]ATATTAACCCTCATC | 90293 |
rs771750455 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117998772 | TGAGAAGCTACTGAC[C/G]ACTGGGTAAAGAAGC | 90293 |
rs771764673 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118115396 | CGATATCGCTAAGAG[G/T]GAGTAGTCTTTTTTG | 90293 |
rs771785237 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048373 | GACAAAAATAATAAG[A/G]GAAATGATAAATACC | 90293 |
rs771788924 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118082170 | GAGATCTATTTAGAT[C/T]TTTTTAGGAACCTTC | 90293 |
rs771789160 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039442 | GAACATCACTGGTAG[C/G]TAGATAGTACTCATT | 90293 |
rs771805837 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117990282 | GAAGAATGAGGATGG[C/G]GGTGTGAATGGATCA | 90293 |
rs771808588 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118106887 | CTTCTCTTAGGGTAT[C/T]ATTTGATTTGTTATT | 90293 |
rs771816832 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117969606 | TCTATCAAGACAATC[A/C]CTTCAGAAATCCACA | 90293 |
rs771820957 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961390 | AATTGGAACACTTTC[C/T]ACAACGCATGTGTAA | 90293 |
rs771830191 | snp | A/G | 0.11536 | 0.210647 | intron-variant | KLHL13 | GRCh38.p7 | X:118009732 | TTGACTTGGCGATGC[A/G]GGCTCTTTTTTGGTT | 90293 |
rs771854232 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:117952330 | ATTTAATAAATGGTG[C/T]TGGGAAAACTGGCTA | 90293 |
rs771872892 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075045 | CTTTTCCCAAGTTCA[A/G]TACACTACAGTTAAT | 90293 |
rs771879685 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026756 | TGATACCCAACACCA[C/T]AGATACCACAGTTGG | 90293 |
rs771907566 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117943628 | TGATTTGGCTATTGA[C/T]ACTTTTGTATGCTTC | 90293 |
rs771911162 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118063886 | ATCTTTTGCTAAAGT[C/T]TTAATGCATATTCTT | 90293 |
rs771912181 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970852 | AGACCAATTCAATAA[C/T]ATAGAGTGTTGTAAT | 90293 |
rs771912990 | in-del | -/C | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975086 | ACATTAGAAGGCTTT[-/C]TGCAATAATCCTTAA | 90293 |
rs771915689 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118020412 | AGACAATTTGGCCAT[C/T]AGAGAAATGCAAATC | 90293 |
rs771916942 | snp | A/C/T | 6.88047e-05 | 0.00586502 | intron-variant | KLHL13 | GRCh38.p7 | X:117920389 | CAACAAGAACATGAG[A/C/T]TGAGTCACTAATCAA | 90293 |
rs771919184 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027230 | TTCTTCACCATAACA[A/G]TGCTTCTGCTCATTT | 90293 |
rs771923225 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033062 | AATAAAAAGAAATGA[A/G]CAAAGCCTCCAAGAA | 90293 |
rs771959175 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041093 | AATCTGAAAGAAAAG[A/G]ATATTATTGAGCAAG | 90293 |
rs771967545 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111895 | AGAGAGCGAGACTCC[A/G]TCTAAAAAAAAGAAA | 90293 |
rs771971834 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921975 | TTATGTTAACAAATA[A/T]CAAATCTTTCACAAA | 90293 |
rs771990849 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118099927 | AAGGAAGAAAGGAAG[A/G]AAGGAAGGAAGGAAG | 90293 |
rs772002942 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117960048 | TTTTAGTGCTCTAAA[-/AC]ACAATATTTTCAATC | 90293 |
rs772006557 | snp | G/T | 4.56673e-05 | 0.00477824 | missense | KLHL13 | GRCh38.p7 | X:117919540 | GATATGAGAAACACT[G/T]TACAGAAGTCCAAAA | 90293 |
rs772018635 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118090444 | AAAAAACAAACAAAC[A/C]ACCCCATCAAAAAGT | 90293 |
rs772024764 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117904985 | ATAGGAATCCAGAAT[C/T]GGTCCCAGAAGAGGA | 90293 |
rs772026852 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923269 | TTTTAAAGTTTTGAA[C/T]AGCTAATGGCAAGTT | 90293 |
rs772053002 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080311 | TCTGCACAGCAAAAG[-/A]AAACTGTCAACAAAC | 90293 |
rs772053720 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112872 | AGGAATAAAGGTATG[C/G]CCATTTGAAAATGTT | 90293 |
rs772068075 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052709 | GGGCGCACCTGTAAT[A/C]GCAGCTACTCAGGAG | 90293 |
rs772073231 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094408 | AAAGACCAAATCTAC[A/G]TCTGATTGGTGTACC | 90293 |
rs772074099 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117981757 | AATTTTTCAGATTCA[G/T]ATTTGTAAAGCACAG | 90293 |
rs772080683 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118100657 | TACTTAAAACTGCCA[A/G]TGGTTTCCCTCAGCA | 90293 |
rs772092876 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911965 | AATTATGAGTCTCTA[C/G]AAATAGACAGCATAA | 90293 |
rs772099093 | snp | C/T | 0.000158115 | 0.00889003 | synonymous-codon, intron-variant | KLHL13 | GRCh38.p7 | X:118028438 | CCGGTTACGAAGTAT[C/T]GCAGCAACCAATTCC | 90293 |
rs772105593 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036682 | CAGGACATAGGCATG[G/T]GCAAGGACTTCATGT | 90293 |
rs772109587 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051695 | ACAAACTCAAAATCA[C/T]AAAGATGCAAACTTC | 90293 |
rs772115328 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117950673 | ACAACAAAACAGGTT[A/G]GTTAATCAAGGCACT | 90293 |
rs772140201 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117995937 | AGCTCTTTCCACCTT[C/T]GGGTATTGTGAATAG | 90293 |
rs772143460 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117962313 | ACATAGAGGTTTGGG[-/T]TTTTTTTTTTTCATT | 90293 |
rs772144143 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902989 | ATAGTTCTGGGCAGC[A/G]ACGGGTAAGCAGAAG | 90293 |
rs772149139 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118020828 | TAAAAATGATGAGTT[C/T]ATGTCCTTTGTAGGG | 90293 |
rs772163348 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036421 | ATGAACAGAACAGAG[C/T]CCTCAGAAACAACGC | 90293 |
rs772173259 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014963 | TGATATATAGTATAA[C/T]AAAACAGTAAGCGCT | 90293 |
rs772180497 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011359 | TGCCACACTGGCAGC[C/T]ACTGAAGAAATCTAA | 90293 |
rs772191426 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118031918 | GCAGGGCAAGACATT[G/T]CCTCACTCAGGAAGC | 90293 |
rs772193776 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958234 | ATACACTACGTTTTA[C/T]TCCTATACATACATA | 90293 |
rs772203692 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118022652 | TTTTAAAATATATCT[A/G]TTCAGGTCCTTTGCT | 90293 |
rs772204899 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117920424 | AAATGAGGTTACAAA[G/T]CTTCGTGTGCTAAAA | 90293 |
rs772215035 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118003189 | ATAGGTTACTGTGCA[A/G]TAGGTTTTTAAAATA | 90293 |
rs772224902 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086098 | GTGCGCCACCACAGC[C/T]GGTTAAATTTGTATT | 90293 |
rs772240363 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118058559 | TCAATAACTATAGCT[C/G]AGTTATGCAACGTGC | 90293 |
rs772255473 | in-del | -/AT | 0.0230396 | 0.104828 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031497 | GATATATATATTTAG[-/AT]ATATATATATACACA | 90293 |
rs772257301 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118077026 | AGAAACATACTTTTG[C/T]TTTATTATTGTATTT | 90293 |
rs772264612 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987155 | ATGAGAAAGGGATAC[C/T]GACAGAAGAGCTGAA | 90293 |
rs772274547 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936438 | CAACCGCCTGCTCAA[A/G]CCAACCAGATGGACA | 90293 |
rs772288259 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094338 | AAGAGAAGTTTAGAG[-/A]AAAAAAGAGTACAAA | 90293 |
rs772304593 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018767 | ATTGATTGTTTGCCA[C/T]TATATCTTCTAAATG | 90293 |
rs772324950 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977447 | AGTTTGTCACCAGTA[A/C]CACCTCACCAAATGA | 90293 |
rs772329427 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117937109 | ATGCCTTTTGAAGCC[A/G]GAGTATGTGTTATTG | 90293 |
rs772343043 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969403 | AAACACTTAGATGTG[A/G]TTGCTCTTTCAGCTT | 90293 |
rs772346508 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117949407 | CAAAGCAAGAGTGCT[C/G]TGCTGATCTGACTTA | 90293 |
rs772360914 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038539 | CATTGGAACTCAGTG[C/T]TACCCTGTCAGAGTA | 90293 |
rs772363201 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117899452 | AAATGCAAAAGTAAT[A/T]AAAGGAGCTCTGTCA | 90293 |
rs772370842 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118024399 | ACAGAAGAAAAATGA[G/T]AAACTGAACTTCATT | 90293 |
rs772374049 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117916400 | TCATTTCATTGTCCT[C/T]TTTTCCATAACTCCA | 90293 |
rs772375953 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092982 | TACTTCCTAATAGTG[A/G]AAAAATTTTAAAACA | 90293 |
rs772422321 | snp | C/T | 2.28196e-05 | 0.00337776 | missense | KLHL13 | GRCh38.p7 | X:117899143 | GCGACCCCAACATCA[C/T]TCTGCCCTCTTAACA | 90293 |
rs772423356 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940461 | AAATTTAAAGTAGCT[C/T]TTTTCTAATTCTGGG | 90293 |
rs772444593 | snp | C/T | 0.085528 | 0.188279 | intron-variant | KLHL13 | GRCh38.p7 | X:118098146 | AGTGAACAGGCAACC[C/T]ACAGAATGGGAGAAA | 90293 |
rs772449032 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000882 | GTAATATAGGATATA[A/C]AGACTGCTACCTTTC | 90293 |
rs772449086 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118096237 | CACAATACAAAATGA[C/T]AAAGGGGGTATCACC | 90293 |
rs772455290 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926125 | AGAGATTCGATTTAC[A/C]TTACGTCCTGAAACT | 90293 |
rs772462255 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118018419 | CATCATAAACAGAAC[A/G]AATATAGATTTTTTA | 90293 |
rs772490912 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118042040 | ATGCAAATGGAAACC[-/A]AAAAAAGAGCCAGGA | 90293 |
rs772505464 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065471 | CAGAAGTGGAACTTG[C/T]CCTAAACTAATTATA | 90293 |
rs772524799 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025287 | TACCCATGGTCAACC[A/G]CATTCTAAAGAAAAT | 90293 |
rs772526620 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118097593 | ACTTTAAAGTTCATA[A/T]GGAACCAAAAAAGAG | 90293 |
rs772537913 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938574 | ATTTGAGAACCATTG[C/G]TTTAAATATCTCTCA | 90293 |
rs772547202 | in-del | -/TTC | 0.0661441 | 0.169402 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117937 | TCTTTGGCTGTTTTT[-/TTC]TTCTTCTTCTTCTTC | 90293 |
rs772553772 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018912 | TATAGATATACAAGC[A/C/T]TAACCTTTTTATTTC | 90293 |
rs772559601 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107012 | TTAACTATTACAAAT[A/G]CTTCAGTATTTTCTT | 90293 |
rs772561994 | snp | G/T | 2.29103e-05 | 0.00338447 | missense | KLHL13 | GRCh38.p7 | X:117909909 | AAGAGCTCAAGTTCA[G/T]TACAGTGCTTAAGGC | 90293 |
rs772563795 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916396 | GTATTCATTTCATTG[A/T]CCTCTTTTCCATAAC | 90293 |
rs772572628 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118081059 | AGTGGGAGCTAAACA[C/T]TGAGCACATATGGAC | 90293 |
rs772575153 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000464 | AAATTATTATTGGCT[A/G]GGGATGAGTGTAACA | 90293 |
rs772575844 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118041427 | AGCTACTAGGGAGGT[A/T]GAGGTGGGTGGATCA | 90293 |
rs772581601 | in-del | -/AAAC | 0.0197025 | 0.0972782 | intron-variant | KLHL13 | GRCh38.p7 | X:118080408 | ATCTATAAGTAACTT[-/AAAC]AAATCAACCAGCAAG | 90293 |
rs772581643 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072634 | CAAACAAATTTACAA[C/G]AAAAAAACAAACAAC | 90293 |
rs772583175 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117905485 | AGCACTAAACCAGGT[A/G]AGCACGTGTGCTAGT | 90293 |
rs772594011 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064688 | GAAAAGTTTAATAAA[C/T]ATACTTTCATACCCC | 90293 |
rs772594242 | in-del | -/ATA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910667 | AAATAATTTAATAAG[-/ATA]ATTATCCCTAGGGCA | 90293 |
rs772607268 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047917 | AAGACAAAATAAGGT[A/G]TTATATGAAGAAAAG | 90293 |
rs772612405 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117908944 | TAAAATATCATATGG[C/T]CTTTTAAAAGCAGAA | 90293 |
rs772614896 | in-del | -/GCAATGTTGTT | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118012075 | TGAAACTGAGACCTG[-/GCAATGTTGTT]GCTTTTTAAAGCAGC | 90293 |
rs772622807 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004620 | CAATAAAATAGGAAA[C/T]TATGATTCCATATTG | 90293 |
rs772624945 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117992227 | TTCTCTTAGAGAAAC[G/T]GAGATGTAAAAAAAA | 90293 |
rs772640973 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962166 | AGGGAGCCATGATCA[C/T]GCCACTGTACTCCAG | 90293 |
rs772651386 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083841 | ACCCCATAAATACGA[A/G]CAATTATCATGTATC | 90293 |
rs772657498 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117932281 | AACAGAAAACCAAAA[C/T]TTATTCTTCCTAACT | 90293 |
rs772658018 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118078204 | CATAATCACAAATGG[A/T]GGTCCAATTTATAAT | 90293 |
rs772667356 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073070 | CTGCACTATCACCTG[C/G]GTTACAGAGTGAGAC | 90293 |
rs772671010 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048555 | CATGGGCAACTGTTA[C/T]ATTGTACTTTTCTGC | 90293 |
rs772676190 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117960363 | CAAGTTTAGAAATGC[C/T]ACTTCTGAGGCCATA | 90293 |
rs772687330 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118115465 | TTATACAAACATGAA[A/G]TCTACTGTTAAGAAA | 90293 |
rs772691542 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039476 | GCCCTGGGGTAAGGA[C/T]GGCCAAAAGGAGTGG | 90293 |
rs772697736 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117982499 | CTCCCCACTGCCCTG[A/G]TTAATATGGTTTGAC | 90293 |
rs772720503 | in-del | -/A | 2.74326e-05 | 0.00370345 | intron-variant | KLHL13 | GRCh38.p7 | X:117910110 | CCTATTAAGCCAATT[-/A]AAAAAAAATTAAAAC | 90293 |
rs772725507 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959755 | ATTATATGATGTCAA[G/T]GTCTTATCTCATTGA | 90293 |
rs772726072 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118062185 | CATCAGGGTCTTGTT[C/T]TCTATCACAATATAG | 90293 |
rs772735815 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060097 | CTCATGGAGAAAACA[A/G]ACATAACAGAGCATA | 90293 |
rs772740902 | in-del | -/AA | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118033416 | AACTCTACAAGCCAG[-/AA]GAGAGTGGGGGCCAA | 90293 |
rs772747966 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118070890 | TAGGTATATCCCCCA[A/C]TGCTATCCCTCCCCC | 90293 |
rs772748934 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117984028 | AGAACAGATGGCTAA[A/T]GTTCTTCTAGGTTCA | 90293 |
rs772755530 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118095964 | AGCACTAAATGCCCA[A/C]AAGAGAAAGCAGGAA | 90293 |
rs772756788 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:118081454 | TGATGTTGATTTTTG[G/T]TTTTTTTTAACTGAT | 90293 |
rs772760873 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117990379 | GTAATCAACTTTCTA[A/C]GTCAAGATAGGATTG | 90293 |
rs772765119 | snp | C/T | 0.126432 | 0.217327 | intron-variant | KLHL13 | GRCh38.p7 | X:118009778 | AGTAGTTTTTTCCAA[C/T]TCTGTGAAGAAAGTC | 90293 |
rs772767746 | snp | C/T | 5.95628e-05 | 0.00545691 | intron-variant | KLHL13 | GRCh38.p7 | X:117901983 | GAAAATTATTTTTAA[C/T]TTCAAATTTAGCAAT | 90293 |
rs772781205 | snp | C/T | 2.49728e-05 | 0.00353352 | intron-variant | KLHL13 | GRCh38.p7 | X:117901785 | GGAAAGATAACCATA[C/T]AGTTAAAAGCTTATA | 90293 |
rs772786566 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118038951 | GTCTTGCAACTTGCA[C/T]ACTAGCTTACCTACA | 90293 |
rs772808802 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082428 | AGAAACAGCTCTTCC[A/G]CTCTTTTGCCAATTT | 90293 |
rs772811967 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117980994 | TCATGACTATTTCCA[A/G]ATCCTTTTCGTTTTC | 90293 |
rs772825651 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117977427 | ATTTGCTAACTGACT[A/G]GTATAGTTTGTCACC | 90293 |
rs772830969 | snp | A/G | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028536 | ATATTTACTATGAAG[A/G]TTAACACTGGAATTT | 90293 |
rs772835120 | in-del | -/A | 2.29964e-05 | 0.00339082 | intron-variant | KLHL13 | GRCh38.p7 | X:117919494 | AGAGTCTACCACAGG[-/A]AAAAATCAGATTTCA | 90293 |
rs772869545 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938907 | CAAACAAAAATAGCC[A/G]AAGACTCGTTTTCAT | 90293 |
rs772880333 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117906473 | CAGGATGTGACGTGA[C/G]AAGACAATCTACTTC | 90293 |
rs772889075 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107046 | TGGGGACTTAAAATC[G/T]GGAACAATTAGAGAT | 90293 |
rs772890883 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118026488 | CTGCTAAAACTGAAG[A/C]AAGAACAAACATCAA | 90293 |
rs772892335 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008196 | CATAATCTTTCTAAC[A/G]CTCACCTTGTAACTG | 90293 |
rs772893309 | snp | A/G | 0.119993 | 0.213537 | intron-variant | KLHL13 | GRCh38.p7 | X:118032825 | TCAAACCAAAGGCAA[A/G]GAAGTTGAAAACTTT | 90293 |
rs772895499 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117928722 | TTTATATCAGTCAAT[-/G]ACTATATTAAAAAAG | 90293 |
rs772896830 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954808 | ATGCTTCGCCCTACA[A/G]CTAGCACCCAGCCTG | 90293 |
rs772911444 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942879 | CATTATGATGCTAGC[C/T]AGTTATTTTGCCCCT | 90293 |
rs772926012 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118018774 | GTTTGCCATTATATC[C/T]TCTAAATGGCGATTT | 90293 |
rs772949274 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041199 | AAATATAATTACAAC[-/T]TTTTCACAGCATAAA | 90293 |
rs772983976 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118041492 | TGAGATCACACCACT[A/G]CACTACAGCCTGGAT | 90293 |
rs772991808 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063475 | TCATTTCCCCTACAC[C/T]GGGCCAATATCTGGG | 90293 |
rs773002386 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050350 | TCCTTGTATTAATGC[-/A]AATTCTATATGATTT | 90293 |
rs773020993 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117952564 | CAAATGGGATCTAAT[G/T]AAACTAAAGAGCTTC | 90293 |
rs773025832 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117988950 | TTTAATAGTTACACT[A/G]AGAATTTGAAAGGGC | 90293 |
rs773032797 | in-del | -/AAAT | 0.00954126 | 0.0684076 | intron-variant | KLHL13 | GRCh38.p7 | X:118011073 | TGAGACACTGTCTCA[-/AAAT]AAATAAATAAATAAA | 90293 |
rs773044446 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020848 | CCTTTGTAGGGACAT[A/G]GATGAAGCTAGAAAC | 90293 |
rs773047729 | snp | A/C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117947330 | GAGCCTAGCACGAAA[A/C/G]ACTTAATATATGTCC | 90293 |
rs773066128 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118028158 | AAATTCAAATAAATA[G/T]CTCCACTGATTGTAT | 90293 |
rs773072300 | in-del | -/GGAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954407 | GGTAGATAGGTAGAC[-/GGAT]GGATGGATGGATGGA | 90293 |
rs773075895 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040220 | ACGAAAATCTACAAA[C/T]GTTGAGACCACCCAG | 90293 |
rs773076067 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118062144 | GGTAGTATTTCAAAA[C/T]AGGAAATATGCTTTC | 90293 |
rs773094317 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117911210 | TTATCAATGTATTGT[C/T]AACCTCACACCTGTA | 90293 |
rs773105397 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118082235 | ACTCCACCAACAATA[C/T]GTAAGTTCCCTTTTC | 90293 |
rs773109690 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118068664 | AAAGCTGTGCTCCCC[C/T]CACAGATAAGAAGCC | 90293 |
rs773120512 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002726 | AAAAGCAAAGGCACA[A/G]AGAAGGGCCTAAAAT | 90293 |
rs773132247 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014601 | ACCCCCTCCCCTTTT[A/C]GAATCCCTAACAAAA | 90293 |
rs773136463 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118086099 | TGCGCCACCACAGCC[A/G]GTTAAATTTGTATTT | 90293 |
rs773155390 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117987690 | AATCTTTCCATCTTA[A/G]TCAACTGTTTTATGT | 90293 |
rs773160066 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117995163 | TTGTGAACTGCCTTC[A/G]TGTGTCATATCAGTA | 90293 |
rs773173544 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117964722 | AGGCATATCTCCTAA[C/T]GCTATCCATCCCCCC | 90293 |
rs773181382 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031524 | ACACACACATATATA[C/T]TTAGTTATATATATA | 90293 |
rs773193133 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083107 | TTCTCTTGTTTTTAT[-/A]AAAAACTATCATTGG | 90293 |
rs773194237 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939806 | TGTTTTTTTCTTGTA[A/T]ATTTGTTTAAGTTCT | 90293 |
rs773196439 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118067645 | TATTTTACTTTTTAA[A/G]CTTTTTTTTAACTAA | 90293 |
rs773204295 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117969636 | ATAGATGGCACACCA[C/G]CCTGCAATGCTAAAA | 90293 |
rs773208911 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118057718 | GTAGTCCCAGCCACT[C/T]GGGAGGCTGAGGCAG | 90293 |
rs773217366 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986237 | TGCAACTGAGGCTGA[A/G]GAATGAAGCATACAT | 90293 |
rs773222341 | in-del | -/CTCT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991853 | ACAGTGAAACTCTCT[-/CTCT]CTCTCTCTCTCTCTC | 90293 |
rs773248392 | in-del | -/TACAATAACAG | 0.000170547 | 0.00923278 | intron-variant, utr-variant-5-prime, splice-acceptor-variant | KLHL13 | GRCh38.p7 | X:117972845 | TTGTCACCACGGTAC[-/TACAATAACAG]TAAAGAGCGTTTCCA | 90293 |
rs773261005 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936462 | ATGGACACCTTATTC[G/T]GTATACCCATAACTT | 90293 |
rs773263672 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023725 | AGGTGTGCACCACCA[A/T]GCCTAGCTAATTTTC | 90293 |
rs773271161 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117920568 | TTCACTGTAGGAATA[A/G]CACAAAATTAAGACT | 90293 |
rs773276269 | snp | C/G | 0.0266548 | 0.112325 | intron-variant | KLHL13 | GRCh38.p7 | X:117903157 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGA | 90293 |
rs773285171 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915669 | TTTTGTTCATTCTAT[A/G]TATTTGTATATTTAA | 90293 |
rs773286107 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968377 | TTCCTGTGTTAAAAG[A/G]GGTTTGGACTTTCTA | 90293 |
rs773294434 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948912 | AACGTGGTCAAACCA[A/G]ACATACACAGACTGT | 90293 |
rs773305866 | snp | A/G | 2.65132e-05 | 0.00364087 | intron-variant | KLHL13 | GRCh38.p7 | X:117910102 | CTAAAGTGACCTATT[A/G]AGCCAATTAAAAAAA | 90293 |
rs773335402 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118104915 | AATTATATCTTAATA[A/G]AGCCGTTAAATATTT | 90293 |
rs773362173 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030196 | TTATTTGTACAATCA[C/T]TTTTCTGCTTATAAT | 90293 |
rs773366346 | in-del | -/TAAC | | | intron-variant | KLHL13 | GRCh38.p7 | X:117976765 | GCATTTTATGAACAT[-/TAAC]TAATCAGTTAAAAAA | 90293 |
rs773381964 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924088 | TGCATAAATGAATGA[A/C]CCCACTATCCAATTC | 90293 |
rs773391529 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117949472 | TTTAATTTGGTAGAC[A/G]TTCTATAGAGAACCA | 90293 |
rs773395813 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925507 | ATGTTTTTATGAGGC[A/T]GCTCTTCATTTTATT | 90293 |
rs773398166 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082617 | TTGATGTAATCCCAT[-/C]CTGTCTATTTTTGCT | 90293 |
rs773427063 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097599 | AAGTTCATATGGAAC[A/C]AAAAAAGAGCCCGCA | 90293 |
rs773445921 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118031939 | CTCAGGAAGCACAAG[A/G]GGTCAGGGTGTTCCC | 90293 |
rs773447437 | in-del | -/TTC | 0.00328766 | 0.0404107 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117938 | TCTTTGGCTGTTTTT[-/TTC]TTCTTCTTCTTCTTA | 90293 |
rs773458214 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117978382 | CCATGTTGGGCAGAG[-/A]AAAAAACAGCAATAA | 90293 |
rs773463151 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940487 | CTGGGAAGAAAGTCA[A/G]TGGTAGCTTGATGGG | 90293 |
rs773479826 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007399 | AAAAAAAAAAGAGAG[A/C]GAGACCTGCCAGCCC | 90293 |
rs773483881 | in-del | -/ATGT | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079271 | AATAAGGCTTAAAAG[-/ATGT]ATAGGAAGTCTAGCC | 90293 |
rs773486522 | in-del | -/AA/AAAAAAAAAAAA | 0.093839 | 0.199232 | intron-variant | KLHL13 | GRCh38.p7 | X:117992234 | GAGAAACTGAGATGT[-/AA/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 90293 |
rs773496048 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117982529 | CATGGAACACAGAAG[C/T]TGCTGAGAGAAAAGT | 90293 |
rs773501279 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118003208 | GTTTTTAAAATACCT[C/G]TATTCAAAAATGAAA | 90293 |
rs773508242 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118112923 | AAAATGATAAGCCCT[C/T]CTTAAAATTCCAAAG | 90293 |
rs773513551 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118097015 | TCCCTTTGAAAACGG[A/G]CACAAGACAGGGATG | 90293 |
rs773522832 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117916412 | CCTCTTTTCCATAAC[G/T]CCAAGAAAATAACAT | 90293 |
rs773526019 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951241 | ATATAAAATAAGCCT[-/G]GCATTTTTGTTGAAA | 90293 |
rs773537575 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118108697 | TGAACTTCAAATCAG[C/T]GAGACAGGCAAGTGT | 90293 |
rs773544063 | in-del | -/AAG | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040703 | TCAATATTCAAGTAT[-/AAG]AAGGTTACAGAACAT | 90293 |
rs773544443 | snp | A/G | 0.0199298 | 0.0978146 | intron-variant | KLHL13 | GRCh38.p7 | X:118091022 | TCTCAGCAAACTATC[A/G]CAAGGACAAAAAACC | 90293 |
rs773547683 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033419 | CTCTACAAGCCAGGA[A/G]AGTGGGGGCCAATAT | 90293 |
rs773554978 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118014067 | CAATATTAAATCAGT[A/G]CACCCTAAGAAAGAA | 90293 |
rs773568506 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117943077 | TTTTATTTATCCTTT[A/G]TTTATGAAGCTTAGT | 90293 |
rs773577759 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079788 | CAGAATTAGAAAAAA[A/C]TATTCTAAAATTCAT | 90293 |
rs773583121 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969415 | GTGATTGCTCTTTCA[A/G]CTTTATTAATTTAGG | 90293 |
rs773585871 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117980477 | TACAACATTCACATG[G/T]GCATCATAAATGTTA | 90293 |
rs773588746 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916408 | TTGTCCTCTTTTCCA[A/T]AACTCCAAGAAAATA | 90293 |
rs773603931 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015920 | GGCTTACAATTATTG[C/T]CACGCTTACTTCACC | 90293 |
rs773613143 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117983091 | TCAAACTTTTTCCAT[C/G]AGGAAGAAGGCAGAA | 90293 |
rs773621136 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118003967 | TGGACTGATGTGGTA[C/T]GGTGAAATGCAAACA | 90293 |
rs773629008 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069421 | AAAAGTTTAAAATGT[-/AA]AAAAAAAAAAAAAAA | 90293 |
rs773634570 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118091729 | GCTGAAAAAGTACTC[-/A]AAGAGATAAGAAACC | 90293 |
rs773643591 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944704 | TAGAAGACATTAATG[A/G]ACATCCAGTACCATA | 90293 |
rs773644554 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115327 | ATTGCAGTATGAAAG[C/T]GAGCAAATGAACCTC | 90293 |
rs773649140 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118018984 | GTTTTGGTACACATA[A/G]ACAGAGTGAAATGAT | 90293 |
rs773651217 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117932446 | CAGTATTTCTCTTTC[A/C]TTGCCTGATTTATTT | 90293 |
rs773658423 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117931268 | AAATGAGAAAATATC[A/T]ACTAGAGGCCCACAT | 90293 |
rs773660365 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922637 | TTGTGTTCGTTTGTG[G/T]TAGTTTGTGGTAGTG | 90293 |
rs773664668 | snp | G/T | 0.000529661 | 0.016265 | downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897382 | AGAAGATCACAATAC[G/T]ATGCTAATATAATTC | 90293 |
rs773694629 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000488 | TGTAACAGTAATGTT[A/G]TACTCACTTCAATAG | 90293 |
rs773707295 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118103864 | TGGCCGAATTTTTTT[-/T]AATTCCAGTTATTTC | 90293 |
rs773714032 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118880 | CCCAAATTTCCAGTG[A/G]GGAGCAAAATAATAC | 90293 |
rs773715490 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117913381 | ATAATAGAATACACA[C/T]TGAAAATATAAAATA | 90293 |
rs773720405 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118092294 | TTAACAAATAAAAAA[A/T]TTTTAAAGCAGTGAA | 90293 |
rs773724471 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084006 | ATGAAATAGAAAACT[A/G]AAACAATAAATGATC | 90293 |
rs773736945 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118012676 | TGTGGCCATCCTGGG[C/G]GGGGGCGGGGGCAGG | 90293 |
rs773746120 | in-del | -/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118001550 | CTGATTGTCAGAACA[-/C]TGGACAAGATGGAAG | 90293 |
rs773753774 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118073100 | CACTCTCTCAAAAAA[A/G]AAAAAACCCCACAAA | 90293 |
rs773766525 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118075974 | AAGACAGTTTTTTTT[-/T]AAGTAAAAGCAAGTT | 90293 |
rs773782823 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118077385 | ATGAGGTTTAAATTA[C/T]TGCCTTGTGGAGGGT | 90293 |
rs773782990 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005259 | AACAATTATTCATAA[C/T]GGCTGGAAACTATCT | 90293 |
rs773791144 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954510 | TGAATGAGATAATTA[C/T]TTTATTTCTAATGAA | 90293 |
rs773812400 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084417 | ATAGCATGAATATAT[C/T]AGAAATAAAAATGAA | 90293 |
rs773813737 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108208 | TTTTACTGAATAGAC[C/T]GTAAAAGCACTTCAC | 90293 |
rs773844718 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117983851 | AAAAGACTAAACTAG[-/C]CAAATTTGGACACAA | 90293 |
rs773845102 | snp | A/T | 2.28045e-05 | 0.00337664 | missense | KLHL13 | GRCh38.p7 | X:117899264 | TGCCACCAATGACAT[A/T]GAGCCTTTCTCCCAC | 90293 |
rs773851361 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118102787 | TCATTCTAAACCATT[A/T]AAGACTTTACCATTT | 90293 |
rs773854532 | in-del | -/GCAA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047022 | GATCTTGTGAGGAAT[-/GCAA]GCAAATACAGCAGGG | 90293 |
rs773863666 | snp | A/G | 2.53094e-05 | 0.00355726 | intron-variant | KLHL13 | GRCh38.p7 | X:117899444 | AATTATAGAAATGCA[A/G]AAGTAATTAAAGGAG | 90293 |
rs773875264 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076750 | CCCCACCCCCAAACA[A/G]GAAGACTGCCTTTGG | 90293 |
rs773883045 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974585 | CAAAATACCAAATTT[A/G]GTATATAAGAAATAC | 90293 |
rs773886307 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117962513 | GAATAGTGCTTCAAG[G/T]AACTATGGAAACATC | 90293 |
rs773891465 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117923751 | CAAACTGCTTGTGGA[A/G]GTATGTAATCAATGC | 90293 |
rs773897338 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016194 | TTCCAATTCTTACAT[A/G]TGACAGATGAGGACA | 90293 |
rs773906655 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975032 | TTAAAAGTTTTTTTT[A/G]ACCTGCCATTAATAC | 90293 |
rs773938049 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118032262 | AGGAGACCTGCCTGC[C/T]TCTGCAGGCTCCACC | 90293 |
rs773942110 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938879 | CCTTAAAAATCTATC[C/T]TCATATGTATAACAA | 90293 |
rs773944834 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117945668 | TCAGTCACTATTGCA[A/T]TCATATGACCATGCA | 90293 |
rs773944967 | in-del | -/AA/AGAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089620 | GAGAGAGAAAGAAAG[-/AA/AGAA]AGAAAGAAAGAAAGA | 90293 |
rs773947110 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117995029 | CTCCAGCCTGGGCAA[C/T]AGAGCGAGACTCTGT | 90293 |
rs773959048 | snp | A/C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118026698 | GAAAAAATTAATCTT[A/C/G]CTCATGCCCTAATTA | 90293 |
rs773963700 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117966234 | ATACAAAATCAATGT[A/G]CAAAAATCACAAGCA | 90293 |
rs773968943 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117959685 | CAAAAGAGTGATTTC[C/T]AAGGTTCCTATCAGC | 90293 |
rs773978317 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101681 | ATTTATAATCCCCAA[A/G]TGTGGAGGGAGGGAC | 90293 |
rs773980724 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021642 | TCCAGTCTATCATTG[A/T]TGGGCATTTGGGTTG | 90293 |
rs773982720 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029797 | AATATGACAACACCC[C/T]GTCTCTATAAAAATA | 90293 |
rs773997160 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938195 | CATTCAATATGTACA[C/G]ATATTACTCTTTTTG | 90293 |
rs774006975 | snp | G/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973135 | CCATACAATGCAGCT[G/T]TATTTAATAAAAGCA | 90293 |
rs774015796 | snp | A/G | 2.30468e-05 | 0.00339453 | missense | KLHL13 | GRCh38.p7 | X:117909973 | AAGGGAGTTTCAAGA[A/G]CTCCCCTGTGCTCAG | 90293 |
rs774019359 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117913949 | TGCTCATTTACATTT[A/C]TTTGATATAAATTAT | 90293 |
rs774022210 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088775 | GATGCATTTTTTTCC[C/T]TATTTCTCCTACAAA | 90293 |
rs774034516 | snp | A/G | | | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909743 | CAAAAGCAAATTCAC[A/G]CAAGTATTGTCAGTT | 90293 |
rs774034982 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118114065 | CTGAAATAATTCCTG[G/T]AAATTTGTTGTATTA | 90293 |
rs774039848 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117925018 | AGAGAGGTACATATC[C/T]AATACCAGGAAACAA | 90293 |
rs774047183 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927189 | ACAGGCCTGAGCTAC[C/T]GCGCCCGGCCACTTC | 90293 |
rs774059071 | in-del | -/TG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118053766 | TGTCCAATCTCAATT[-/TG]TGTGTGTGTGTGTGT | 90293 |
rs774072237 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118095380 | ATACAGGAGCACCCA[A/G]ATTCATAAAGCAAGT | 90293 |
rs774078345 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102275 | AGCAGAGACTATTAG[-/A]TTATTCCCCAATATC | 90293 |
rs774083542 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117987477 | GAAACATGTCCTTGG[A/G]TCTAAATATTTAGTA | 90293 |
rs774088330 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045757 | GATTGCAGTGAGCTG[A/G]GATTGAGCCACTGCA | 90293 |
rs774099970 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117918775 | TTCTATGGAATCAAG[A/G]CTTACATTCTTACAG | 90293 |
rs774100303 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118064923 | TAAATGTTGGGTCTC[-/AT]ATATCTTCCCTTCCC | 90293 |
rs774110697 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117904611 | TACATTTTTTACACA[C/T]TGAAAAAGAATCAAG | 90293 |
rs774124498 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118105588 | GGCTGCTTGGTAATA[A/G]TATTAGTATTGGCCG | 90293 |
rs774149358 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032461 | CAGCCTAACTGGGAG[A/G]CACCCCCCAGCAGGG | 90293 |
rs774160569 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118017086 | ACACAGCCACCAAAG[C/T]GATCTTTCTAGCAGT | 90293 |
rs774164614 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089351 | CTCTCAGGCAGGGAG[A/G]TATCACTGGAGGTCT | 90293 |
rs774168198 | snp | C/T | 0.0183711 | 0.0940641 | intron-variant | KLHL13 | GRCh38.p7 | X:118095830 | CAGAAATAAAGATGT[C/T]CTTTGAAACCAATGA | 90293 |
rs774183755 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118001453 | AAGTACCTACAACTC[G/T]AATCCAAATCTAACT | 90293 |
rs774210635 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118106657 | TACCTGGTCTTTTCC[C/T]TTCTGTGCACCTGTG | 90293 |
rs774224130 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117979143 | TACCACGTTGGCCAG[G/T]CTGGTCTTGAACTCC | 90293 |
rs774225395 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117919275 | ACGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 90293 |
rs774227947 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117989155 | TTTACTTGCTTTAAA[C/T]GTCAGTTTAACCTCA | 90293 |
rs774265140 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118093196 | TCTTCTTGTATAAAC[A/G]TCTTAAATAAAATGG | 90293 |
rs774286171 | snp | A/C | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986255 | ATGAAGCATACATCA[A/C]GTGAACTCTAGAAGA | 90293 |
rs774297679 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118035960 | AACAACAGACAAACA[A/G]AGAGCCAAATCATGA | 90293 |
rs774310212 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117964660 | GTTACATATGTATAC[A/G]TGTGCCATGTTGGTG | 90293 |
rs774315310 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117956703 | GACTCTCAGTGTAGA[C/T]GAGAAGCAGACAAAA | 90293 |
rs774316250 | snp | C/T | 6.87033e-05 | 0.00586063 | missense | KLHL13 | GRCh38.p7 | X:117909511 | GAAAATTTCCAATGA[C/T]GGCGATGCCATGCTG | 90293 |
rs774321624 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971407 | CCATTAACTTCTCAC[C/T]TCCATTAACTTGTCA | 90293 |
rs774333597 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951797 | AGCACTGTGCCAGGC[A/G]CATTCTAGTATCCTA | 90293 |
rs774336343 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117908655 | AAAGTACATTTATGA[A/C]CAATTTTATACTGGG | 90293 |
rs774352249 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117910181 | ACCTGTTCTAGAATA[A/C]GAGTAAATTATGCTT | 90293 |
rs774354393 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117980086 | TCACTTATTTTTTTT[A/T]ATTTTGGTAGCATCA | 90293 |
rs774369923 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118066773 | AGAATCAATAAAAAA[A/T]TTACAACTCTACAAT | 90293 |
rs774370118 | in-del | -/AATAAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085028 | CTCTGTCTAAAAAAT[-/AATAAT]AATAATAATAATAAT | 90293 |
rs774377531 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117924869 | TGCTATTTTGATGCT[A/G]GAAAATAGCATTTTA | 90293 |
rs774397581 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052228 | ATCGTAAAAGAAGTA[C/G]AGGGCCGGGTGCGGT | 90293 |
rs774414424 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117976614 | CCCACTACTTTAATA[A/T]TTAGAATAGCAAATG | 90293 |
rs774416700 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117945279 | TAGAGCCATTTTGGG[A/T]TCACAGCAAAACTGA | 90293 |
rs774418222 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942402 | AATTTTCTGTCTCAT[C/T]AATCTGTCTAATATT | 90293 |
rs774437566 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049138 | TTAGCCAATTTCACA[C/T]TACATAAGGTAAGTC | 90293 |
rs774462493 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073768 | AGCTTACTTTTGTAA[A/C]TTTTACTCACTTCCA | 90293 |
rs774472953 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942801 | CAGTCTGTGTCTTTT[A/C]ATTGGGGCATTTAGC | 90293 |
rs774476201 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118096572 | AATCCTCCCTAACTC[-/A]TTTGATGAGGCCAGC | 90293 |
rs774483957 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117995043 | ATAGAGCGAGACTCT[C/G]TCTCTAAAACAATAA | 90293 |
rs774492874 | in-del | -/AAAGAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089631 | GAAAGAGAAAGAAAG[-/AAAGAAA]GAAAGAAAGAAAGAA | 90293 |
rs774519657 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118058495 | CGTCTTGATCTTTCA[A/G]AACAATTATAATCCT | 90293 |
rs774547967 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118093958 | TGAGCGACACAGAAG[A/T]CGGGTAATTTCTGCA | 90293 |
rs774558325 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118104113 | TGTGTTCCCAGCTAC[C/T]CAGGAGGTTGAGGTG | 90293 |
rs774560890 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998406 | ACATAAGAAATTATT[A/G]ACTATGACAGAGGGT | 90293 |
rs774576286 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111614 | AATAAAAAGTTAGGC[C/T]GGGAGCAGTGGCTCA | 90293 |
rs774592143 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031458 | AGATATATATATAGA[C/T]ATATATATTTAGATA | 90293 |
rs774603853 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117934793 | TTTGTTTTGGTTTGT[C/T]TTCTTCTTTCCTGGT | 90293 |
rs774608652 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948002 | AGTTAAATACAATAT[A/G]CATACAAGTCATTCT | 90293 |
rs774609487 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048760 | TATTGTAATTAAAAA[G/T]GCACACTTTCCCCTG | 90293 |
rs774614458 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000805 | TATTCTTATATTTCA[C/T]TGCAGTAACATTACT | 90293 |
rs774630649 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085566 | CCCCACAGACAGTTT[C/T]TCATCCCTCATTCTC | 90293 |
rs774648843 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118017645 | TTATACACAGTCAGT[A/G]GCACCCCATATGTCC | 90293 |
rs774657222 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014040 | ATTGATTGTAAAATA[C/T]GTGTGTTTGAACAAT | 90293 |
rs774664918 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940411 | TTTTGCTTAGGATTG[A/T]CTTGGCTACACGGGC | 90293 |
rs774666526 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117947171 | CTTTTGTGGACAGAC[A/G]TTTAAAATTACAGAA | 90293 |
rs774675529 | snp | C/T | 4.75031e-05 | 0.00487333 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117898941 | GGACTCTCTAGAAGG[C/T]GATGGTGTGGTTTCT | 90293 |
rs774681986 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118023672 | CTCCCAGGTTCAGGC[A/G]ATTCTCATGCCTCAG | 90293 |
rs774684751 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117904558 | TCCAGTCTACTTCCT[C/G]TTTTGTAGGGCCCAA | 90293 |
rs774686127 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029959 | GGTGGTAGAGTGAGA[A/C]CCTGTCTCAAAAAAT | 90293 |
rs774705888 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117932825 | ACTAATTTACATTTC[C/T]ACCAACAGTATTTAA | 90293 |
rs774715611 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118048303 | AAACAAGTACACATA[G/T]GTACACACATATACA | 90293 |
rs774730010 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117958980 | GGCTATCTGCAGGGC[C/T]GGATCAGCAATCACA | 90293 |
rs774738130 | in-del | -/CTAA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117977417 | GTAAAACTTAATTTG[-/CTAA]CTGACTAGTATAGTT | 90293 |
rs774746656 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991551 | ATGTATTTGTAGACT[C/T]CACTTTCAAGGTCCC | 90293 |
rs774762550 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118106790 | TTAAAAGATTAGTCT[A/C]TCCCTCTAACACCTA | 90293 |
rs774765917 | snp | A/G | 0.0575773 | 0.159604 | intron-variant | KLHL13 | GRCh38.p7 | X:118096923 | AGGTATTGATGGGAC[A/G]TATCTCAAAATAATA | 90293 |
rs774766289 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117999002 | GATTTGATATGTTAA[A/G]GTGGTCACCATTGTC | 90293 |
rs774802927 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907707 | CAATTATTAAAATAT[A/T]TTGGAAAACCTATGC | 90293 |
rs774811683 | in-del | -/AA | 0.000124727 | 0.00789608 | intron-variant | KLHL13 | GRCh38.p7 | X:117901952 | TCTACTGTGGCTGTT[-/AA]AAAAAAAAAGAAAAG | 90293 |
rs774816110 | snp | A/T | 0.0147244 | 0.0845304 | intron-variant | KLHL13 | GRCh38.p7 | X:117953108 | GACACATGCACACGT[A/T]TGTTTATTGCGGCAC | 90293 |
rs774819401 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011779 | TTGGACATTGGATAT[G/T]TCATGTTTACAATAC | 90293 |
rs774831024 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007188 | CCCAAGTGGGAGGAT[C/T]GCTTGTGGGCCAGGA | 90293 |
rs774836897 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082871 | TCCTTTCCCTCACTG[A/T]ATGTTCCTAACACCT | 90293 |
rs774837940 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117960318 | GTTTGGTAACCAGAT[A/C]TGAGATCAGAACTTT | 90293 |
rs774851686 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118090748 | ATCTAGAACTAGAAA[C/T]ACCATTTGACCCAGC | 90293 |
rs774859042 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044048 | AGTAAAGCTGCAGGA[C/T]ACAAAATCAACATAA | 90293 |
rs774890245 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083732 | TCAAATGTTCTCACC[A/G]TGAAGAAATGACATG | 90293 |
rs774906545 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118079734 | AAGCAATTTACAGAT[G/T]CAACGTTATTCTTAT | 90293 |
rs774910109 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083908 | AAATAGATGCACTAT[C/G]CATCTAGTTTAATAA | 90293 |
rs774910888 | snp | C/G | 2.28071e-05 | 0.00337684 | missense | KLHL13 | GRCh38.p7 | X:117920270 | AAGTAATCACTAGCA[C/G]ATGCCATCATGACTC | 90293 |
rs774914132 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023577 | CCTTCATATATTCCA[C/T]TTTTCTTTTTTGACG | 90293 |
rs774914568 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968300 | AGGTAGTGAGCCCTT[A/T]GTCAGTGACAGTGTT | 90293 |
rs774915200 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117982022 | CCCCTAGAAAGGAGA[C/T]ACATGCTCAGTGAGT | 90293 |
rs774919930 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118072582 | TCACAACCTACTCAT[C/T]TGACAAAGGGCTAAT | 90293 |
rs774921388 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118115093 | CTCTTTTACCGTTAA[A/G]TATGAGGATATTAAT | 90293 |
rs774927751 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117982282 | AAAACAACTGGGAGA[C/T]GTTATTAAAATATCA | 90293 |
rs774942830 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118101121 | TTACACATCAATTGT[G/T]TGTGCCTTCTATAAT | 90293 |
rs774951275 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118116995 | CGGAACTCCCAGGCT[A/G]TAGCGAAAGCGTGAC | 90293 |
rs774962583 | snp | G/T | 4.56017e-05 | 0.00477481 | missense | KLHL13 | GRCh38.p7 | X:117909709 | GCATATATGGCATCA[G/T]TTGGTAATTGCTGGC | 90293 |
rs774967607 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969226 | CTTGCCACACTATTA[C/T]TGTCAAAACTCGCTG | 90293 |
rs774973793 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040566 | ACAATATCTAGAAAA[C/T]AGTCTCAAAAGGGCA | 90293 |
rs774998130 | in-del | -/T | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118076733 | ACTGCTCCTTTTCTG[-/T]CCCCCACCCCCAAAC | 90293 |
rs775000998 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118053479 | GGAACATCACACACT[A/G]GGGCCTGTTGTGGGG | 90293 |
rs775011322 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118099762 | CAGTGAGCTGAGATG[A/G]TGCCACTGCACTCCA | 90293 |
rs775030682 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094622 | AATGAAGGAAAAAAT[A/G]TTAAGGACAGCCAGA | 90293 |
rs775033911 | snp | A/G | 2.35181e-05 | 0.00342906 | intron-variant | KLHL13 | GRCh38.p7 | X:117945387 | CAAAATCCATGGTGG[A/G]TTTTTTAAAGCTACG | 90293 |
rs775041746 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973192 | AATACCATTGTTCTA[C/T]CTTAACAGGGATACT | 90293 |
rs775057271 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118021516 | GTCCTTGTGATAGTT[C/T]GCTGAGAATGATGGT | 90293 |
rs775061997 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033124 | GTCTGACTGGTGTAC[C/G]TGAAAGTGAGGGGGG | 90293 |
rs775063276 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118036837 | GAAAATTTTCACAAC[C/T]TACTCATCTGACAAA | 90293 |
rs775073200 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117953574 | TAAAATAAAATAAAA[A/T]AATAAAATAAAATAA | 90293 |
rs775083094 | snp | C/T | 0.000529661 | 0.016265 | missense, intron-variant | KLHL13 | GRCh38.p7 | X:118028437 | ACCGGTTACGAAGTA[C/T]TGCAGCAACCAATTC | 90293 |
rs775083497 | snp | C/T | 2.29371e-05 | 0.00338645 | missense | KLHL13 | GRCh38.p7 | X:117898987 | GTGAGTGTGCAAGCA[C/T]GAATGCCACCAAGGG | 90293 |
rs775092977 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117973928 | GACCACTCCAAAGCT[A/C]AACAGCGGGTCCGGT | 90293 |
rs775096346 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030810 | GATGCCAGCCTCTTT[-/T]ATCTTGAACGTCCTA | 90293 |
rs775108652 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:117921620 | GCATTGATTACTCTG[C/T]CCCCTTCATATTTTA | 90293 |
rs775111770 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076045 | GCAGAACAGACCAGT[G/T]TCTAATTTTATGTTT | 90293 |
rs775116159 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045566 | CCCAGCACTTTGGGA[A/G]GCTGAGGCTAGTGGA | 90293 |
rs775129038 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975178 | GAAGGAGAAATACAT[-/AC]ACACACACACACACA | 90293 |
rs775154090 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923965 | TGTCTTTTATTCCAC[A/G]CTTAATGTATCTACC | 90293 |
rs775165985 | in-del | -/AG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911442 | ATGGGATATACATGC[-/AG]AACGTGCAGGTTTGT | 90293 |
rs775168769 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117937499 | TTACACTTGTTTTGT[A/C]AGCTGTTATATATTT | 90293 |
rs775169883 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108799 | ACCTCTAGCCTTTTT[A/T]AAAAATTTTTTTAGA | 90293 |
rs775171532 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118058327 | TCTCTTACACACACT[A/G]ATTAATTAAAGTATG | 90293 |
rs775173038 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | KLHL13 | GRCh38.p7 | X:118020998 | GACTGTTGTGGGGTG[A/G]GGGGAGGGGGGAGGG | 90293 |
rs775175314 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117965160 | TCCCTGAGGAATGGC[C/G]ACACTGACTTCCACA | 90293 |
rs775176878 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045761 | GCAGTGAGCTGAGAT[G/T]GAGCCACTGCACTCC | 90293 |
rs775191236 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113725 | CTGTATCATATTCCC[C/T]TACTTATTTTCATTG | 90293 |
rs775196694 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118003788 | AGGTGGCAACAACTC[A/G]TCAAAGTACAGAAAA | 90293 |
rs775210012 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117903256 | CATCAAATTCACTAC[A/G]CAAAGTATGCTTTTC | 90293 |
rs775210831 | snp | A/T | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972897 | CAACTAAGACTTCCA[A/T]TCCACACTGTACTGA | 90293 |
rs775217132 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118109272 | GTACCCTTGAAATTG[C/T]GCAACAGAGAAAAAC | 90293 |
rs775233471 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922560 | ACAAGTTAACTGGAA[A/T]CCAGGAACTTATTTG | 90293 |
rs775262339 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118015484 | AAATGAAAGGTCTTT[A/C]GTATGTAGGCAAGGA | 90293 |
rs775271806 | in-del | -/ATGCA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114454 | ATAAATAGTCTTACT[-/ATGCA]ATCACATTAGCAGCA | 90293 |
rs775291614 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117926427 | CTCAAGGATTCCAGC[A/G]AGTAATGATAAACAT | 90293 |
rs775315735 | in-del | -/CAGA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117996296 | CAGTAGCAGATGATT[-/CAGA]CAGTTTGCTAAATTT | 90293 |
rs775320434 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088335 | CAATAATGTATACGT[C/T]AATCATTACTTAAGC | 90293 |
rs775325216 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118057065 | AAGGTAATCACAGCA[G/T]AACAAAGCTGGAAGA | 90293 |
rs775325563 | snp | A/G | 4.56152e-05 | 0.00477551 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117899213 | AGTATTCACAGCTTA[A/G]GACATCATCATAATC | 90293 |
rs775326858 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118095208 | AAGATCTACCAAGCA[A/C]ATGGAAAACAAAAAA | 90293 |
rs775347155 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117927058 | CTATAGGCGCATGCC[A/G]CCACGCCCGGCTAAT | 90293 |
rs775349186 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118008195 | ACATAATCTTTCTAA[C/T]GCTCACCTTGTAACT | 90293 |
rs775349719 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113236 | TAGCATACTGATCAT[A/T]GAGTTTTTTTTATTC | 90293 |
rs775360149 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080455 | AAAAAAACGGGCAAA[-/G]GACATGAACAGACAT | 90293 |
rs775368890 | in-del | -/A | 0.150308 | 0.229263 | intron-variant | KLHL13 | GRCh38.p7 | X:117997240 | CACACTCTCTTATGG[-/A]AAAAAAAAAAAGAGA | 90293 |
rs775380517 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118073188 | TTCATGCTGCTGATA[A/G]AGACATACCAGAGAC | 90293 |
rs775392945 | in-del | -/TGGC | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117980022 | GAACAGTTAAGAATA[-/TGGC]TGGCTCTATTGAATG | 90293 |
rs775410362 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080723 | CTCAAAGAACTTAAA[A/G]CAGAGTTACCATTTG | 90293 |
rs775418757 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005203 | GTCCTGGAACCAATG[C/T]CCCACAGATAACAAC | 90293 |
rs775437651 | in-del | -/A | 0.00738971 | 0.0603345 | intron-variant | KLHL13 | GRCh38.p7 | X:118105003 | GCTGTCAGTAAAAAG[-/A]TTGTCAATTTGTTTT | 90293 |
rs775462376 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118042300 | TTGGACACATCACCC[A/C]GACTGAAAAATCAAC | 90293 |
rs775470207 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050588 | TCCTTCTTTCTTTCC[C/T]TCTCTCTCTCTCTCT | 90293 |
rs775474661 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117993256 | TTGCAATTGTGACAA[C/G]ATAAGATCTTAAACT | 90293 |
rs775476681 | snp | A/G | 2.30075e-05 | 0.00339164 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972792 | GAACTGGGAATTTCC[A/G]GATAGCAGGAGAGCT | 90293 |
rs775498397 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902639 | CATAATGTATTTTGG[A/G]GAAGTGACCTCAACT | 90293 |
rs775505314 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117933706 | TAGCATCTCTTTTAA[C/T]GATAACTAGTATGTT | 90293 |
rs775510443 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117970500 | TTGCCAGCCAAACAA[C/T]TGTGAGAACAAATAT | 90293 |
rs775517009 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117935601 | GGAAGGTGAAACAGG[C/T]GTATCTGACATGGTG | 90293 |
rs775550420 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117963019 | ACATTTTAAAAATTT[A/G]GAATATGTCTCATGA | 90293 |
rs775550810 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117951296 | ATATTGAAAGATTTG[C/T]CCCCCAACTAAAATG | 90293 |
rs775552058 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118072251 | TCCCTATTTAATAAA[C/T]GGTGCTGGGAAAACT | 90293 |
rs775556015 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118077675 | CAAAGTTGCTTCTGT[A/T]TGGGGACACCACAGC | 90293 |
rs775579855 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070301 | TCACACGTTTTGCTA[G/T]GCAGTGTTTGTTATT | 90293 |
rs775584155 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073972 | GAGGAAACTGGGGTC[C/T]TCATAGCTAACTAAT | 90293 |
rs775602142 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117954307 | CCAAAAATGTTTTCT[A/C]TTTAGAAAGCTTAGT | 90293 |
rs775604271 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941475 | TGGTCCTGGGCCTTT[C/T]TTGGTTGGTAGGCTA | 90293 |
rs775612078 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025635 | CTTTAAGTGAAAGGG[C/T]CAAAGTTCTTGACTT | 90293 |
rs775613437 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117909245 | CTTATTTTATGATTT[C/G]ATAAGAATTTCTGAG | 90293 |
rs775643215 | snp | G/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986133 | TGAGGGAAGCAGGCA[G/T]GTATTCTGACAATAC | 90293 |
rs775651283 | in-del | -/GAGT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118111875 | CCAGCCTGAACGATA[-/GAGT]GAGAGAGCGAGACTC | 90293 |
rs775667724 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:118035034 | ACACTCTCCCAAGAC[C/T]AAACCAGGAAGAAGT | 90293 |
rs775676505 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117995625 | TTAATCAACTCCAAA[A/C]TAAAACCCATACCCA | 90293 |
rs775684436 | snp | C/T | 0.0126344 | 0.0784702 | intron-variant | KLHL13 | GRCh38.p7 | X:117963970 | CACCGCATATTCTCA[C/T]TCATAGGTGGGAATT | 90293 |
rs775698260 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039901 | AAAGAGAGAGAGAGA[A/G]ACTCCATTTGTTTGG | 90293 |
rs775701902 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118026222 | ATTTTAAAATACCTC[A/G]GAATTGAAAAACACA | 90293 |
rs775729270 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900479 | GGAGTTGGAGCTCTC[A/T]TTATAATGGTACAGC | 90293 |
rs775732095 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118095977 | AAAAGAGAAAGCAGG[-/AA]AAAGATCTAAAATTG | 90293 |
rs775755740 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118035648 | ATCATACTGAATGGG[C/T]AAAAACTGGAAGCAT | 90293 |
rs775756062 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043179 | TACAACCTAGTGACA[C/T]TGACCCATGAAAAAA | 90293 |
rs775783650 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092454 | ATCCTATATCAAGCA[A/C]AAACAAAATCTTCAG | 90293 |
rs775783797 | in-del | -/AA | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099274 | TTTTGAAGGTTTCCC[-/AA]AAAAAGTTGTACAAA | 90293 |
rs775790848 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118084674 | AATGTCTCTATGTAG[G/T]AGACTATTTAGATAA | 90293 |
rs775805734 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047341 | TATTCAATCTGATCA[A/T]AGAAAAAAATTAAAA | 90293 |
rs775815236 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102375 | CTTAGGTATCACCAT[A/G]GGATTAAGTTCTGGC | 90293 |
rs775816820 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898756 | TAGGCCAAACAAAGA[A/G]CACAAATAACATCAA | 90293 |
rs775817252 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111520 | CCCAGCACTTTGGGA[G/T]CCCGAGGTGGGTGGA | 90293 |
rs775819759 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117919836 | TATAAGCAGTCATAT[G/T]AGAGTCAGTCTGCTG | 90293 |
rs775822055 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118022808 | CGTTTTGTTTATTGT[A/T]TTCCTTCCCATGAAG | 90293 |
rs775826401 | in-del | -/C | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117967431 | TCTCCCCAAGTTTGG[-/C]CATACTTAAGTCTCA | 90293 |
rs775831413 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048641 | GCCCTGAAGTCGGGA[A/C]TATGTAGATGTGCAG | 90293 |
rs775832412 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117946792 | TTTTTTTCCTGTCAT[A/G]CCTAAAACCCCAAGT | 90293 |
rs775850835 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117947780 | ATGTTAACCTTCTTA[A/G]CAGATTCAATATTCC | 90293 |
rs775862010 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117956429 | TTGGGTAGAACATAC[C/T]ATTGTGATAAAAATG | 90293 |
rs775865509 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117900512 | CTGCCCACATAAAAT[A/C]GATAGATGGTGTAAA | 90293 |
rs775884859 | in-del | -/AAAGAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089635 | GAGAAAGAAAGAAAG[-/AAAGAA]AGAAAGAAAGAAAGA | 90293 |
rs775886570 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957068 | CACCAAAATTATTTG[A/G]CCACCTTTGACCCTT | 90293 |
rs775893403 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118005693 | GTGGCCTCTGGACGC[A/T]GGGAAAGGCAAGGAA | 90293 |
rs775919088 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073638 | ATGTAGAATATAACA[A/C]TAGAAAGTCATAGAA | 90293 |
rs775934997 | in-del | -/AC | 0.176855 | 0.23906 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975193 | CACACACACACACAC[-/AC]ACACACACAGCCACA | 90293 |
rs775943243 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056852 | CCTCAAGTTTGTTGT[C/G]AGGATATATGAACAG | 90293 |
rs775949141 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922345 | GTGAATGAGGACACT[A/C]GGGTGTGGGAGAGGA | 90293 |
rs775951205 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117960707 | TTCAATCTGATTTTG[A/T]ACAGTCTTTTGAATA | 90293 |
rs775970576 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070923 | TCCCCCACCCCACAA[C/T]AGTCCCCAGAGTGTG | 90293 |
rs775971406 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118062758 | CTAATTAAACAAACT[G/T]CTACAAAATGTTTAA | 90293 |
rs775974902 | snp | A/G | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118028690 | AAACTGAAAGTAAAA[A/G]TATCTATGAAATTTA | 90293 |
rs775977527 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118096865 | CAGAAAAGGCCTTTG[A/G]CAAAATTCAGCAACG | 90293 |
rs775979160 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117979205 | CCAAATTGCTGGGAT[C/T]ACAGGCGTGAGCCAC | 90293 |
rs775990241 | snp | A/G | 4.57865e-05 | 0.00478447 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909485 | ATTACTCTGTCCGCC[A/G]ACCACATAGAGAAAA | 90293 |
rs776009157 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | KLHL13 | GRCh38.p7 | X:117998913 | TATATAAATATATAA[A/G]TTTTATATAAACAAC | 90293 |
rs776029067 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104919 | ATATCTTAATAAAGC[C/T]GTTAAATATTTTTTT | 90293 |
rs776057935 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117975977 | CATACTTTTGTCGAA[C/T]TTCATTGGGCTCCAA | 90293 |
rs776058093 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071253 | GCGGCATGATTTATA[C/G]TCCTTTGGGTATATA | 90293 |
rs776059406 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118090584 | CACAATGAGATACCA[A/T]CTCACACCAGTTAGA | 90293 |
rs776060118 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118062547 | AAAACTTTTTGTTTT[A/T]AAAAAAAAAGAAGTA | 90293 |
rs776060732 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118079184 | AATTGTAAATTCGCA[G/T]AAAAAGAAATGTGAA | 90293 |
rs776064641 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117941748 | CATTAATCTGGCTAG[C/T]GGTCTATCTATTTTG | 90293 |
rs776068896 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000746 | AAGCTTGACCTGAAC[A/T]GACATGAGGCTATTC | 90293 |
rs776078306 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938962 | TTTTTTTTTTATACT[G/T]AAAGTTCTGGGATAC | 90293 |
rs776108543 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118029740 | TTGGGATGCCAAGGC[A/G]AGCAGATTGCTTCAG | 90293 |
rs776114808 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117927723 | AAGTAAAAGAAACCA[G/T]CCCCAAAAGCTTACA | 90293 |
rs776116266 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118023484 | CTCATTACATCTATG[C/T]ATTCTATGAATAACT | 90293 |
rs776171238 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089997 | GAGGCAGAAGAATCG[C/T]TTGAACCGGGGAGGC | 90293 |
rs776171464 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117964597 | GAACTGAGCACTTTC[-/T]TTTTTTTTATTAAAG | 90293 |
rs776175488 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083627 | CAACAAAAAGTTACA[A/G]TTAGATAGGAGGAAT | 90293 |
rs776175711 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118100134 | AGCTCTGCTTATTGT[C/T]CTTCTTATTTTTGCC | 90293 |
rs776184955 | snp | C/T | 2.81956e-05 | 0.0037546 | intron-variant | KLHL13 | GRCh38.p7 | X:117909292 | TATGCTTAATATAAA[C/T]GCACTTACGCAGTTC | 90293 |
rs776185106 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118115703 | CCAATCCTCTCTCTC[A/G]GGCCTGCTCAGCAGC | 90293 |
rs776188582 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118028341 | TATACCAAGTATTCA[A/C]CAAATATTTATTGAA | 90293 |
rs776198789 | in-del | -/T | 2.50492e-05 | 0.00353892 | intron-variant | KLHL13 | GRCh38.p7 | X:117945582 | CGAGAGATCTGAAAG[-/T]TTTTTTTACATAAGA | 90293 |
rs776204076 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118017970 | CCGCCACAACAACAA[A/C]CTGGTGACTCTCACC | 90293 |
rs776204735 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082643 | TTGCTTATGTTGTCT[A/G]TGCTTTTGAAGCTTA | 90293 |
rs776216852 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027439 | CCAGGACGCTCAGTT[A/C]TTTAAATGGCTGGTA | 90293 |
rs776228596 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113538 | GTCTCTTTTTCCCCC[C/G]TCAAGGCCTTGGCTC | 90293 |
rs776249284 | snp | G/T | 0.0110639 | 0.0735497 | intron-variant | KLHL13 | GRCh38.p7 | X:117952657 | TGCAACCTACTCATC[G/T]GACAAAGGGCTAATA | 90293 |
rs776251174 | snp | C/G | 2.28123e-05 | 0.00337722 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117919590 | ACTGGCAGCTTCCAG[C/G]GTGTCTTGAAGGTTG | 90293 |
rs776252177 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972992 | CAATCTGTAAAATAG[A/G]GCTGTAAGGTACCTC | 90293 |
rs776260618 | in-del | -/AATG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117920410 | CACTAATCAAGGTAA[-/AATG]AGGTTACAAATCTTC | 90293 |
rs776274532 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117995257 | AAACTAATAATTTCT[-/C]CATAAAAAGAAGACA | 90293 |
rs776275335 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117981158 | TTAAAATTGCTGTGC[C/G]TGCAAACAGAAATTC | 90293 |
rs776278755 | snp | A/C | 2.32588e-05 | 0.00341011 | missense | KLHL13 | GRCh38.p7 | X:117898965 | GGTTTCTTCTGGTGG[A/C]AAAACTGTGAGTGTG | 90293 |
rs776279306 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118010010 | ATCATCACTGGCCAT[C/T]AGAGAAATGCAAATC | 90293 |
rs776283998 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939992 | TGCCATTGCTTTTGG[C/T]GTGTTAGTCATCAAC | 90293 |
rs776302590 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117953529 | TGCACATTGTGCACA[G/T]GTACCCTAAAACTTA | 90293 |
rs776302714 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117943826 | TCTAAAGCCTACTTC[C/T]GTCAGTTTGTCAAAC | 90293 |
rs776307777 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117929954 | GTGACAGAATGAGAC[C/T]TTGTCTCAAAAAAAA | 90293 |
rs776314003 | in-del | -/CT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117939901 | TAGGATTCCTGTACA[-/CT]CTGATGATAGTTTCT | 90293 |
rs776325425 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936623 | ACCATGACTCCTACC[A/C]TCACTGTTCTGCTCT | 90293 |
rs776327603 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117986339 | TCAGCAAATTCTTCG[A/C]TATGACTGAAAAGAG | 90293 |
rs776328779 | snp | G/T | 0.00791544 | 0.0624105 | intron-variant | KLHL13 | GRCh38.p7 | X:117972024 | CTGCAAATTTAAAAA[G/T]ATTTTCAAAAATTTT | 90293 |
rs776375154 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118108482 | GAGCAAATTAAACCA[C/T]CACGTTGTAACAGGC | 90293 |
rs776380140 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118008531 | GAAAGGGACACCTAA[C/T]TCTGCTAGGAAGAGA | 90293 |
rs776384963 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118094090 | CTCTGAGCTAAAGGA[A/G]GAAGTTCGAACCTCC | 90293 |
rs776388171 | snp | C/T | 2.29074e-05 | 0.00338425 | missense | KLHL13 | GRCh38.p7 | X:117909457 | CAACTGCCGTTTTTC[C/T]TTTTGTATCATAATT | 90293 |
rs776397670 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118020912 | AACCAAACACCGCAT[A/G]TTCTCACTCATAGGT | 90293 |
rs776407152 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118053399 | GCAAGGACAAAAAAC[C/T]AAACACCGAATGTTC | 90293 |
rs776409605 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117911400 | ACATTGTTATTTTCA[C/T]AGATTATTTTAATTA | 90293 |
rs776413638 | in-del | -/AGAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040510 | AGGTTATTTGAAAAT[-/AGAG]AGACAAAAGAAAAAA | 90293 |
rs776416467 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118069531 | AAAATTGAACTTGTA[C/T]CCCTTACATTTATAC | 90293 |
rs776452827 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118024270 | CACTTCTCTGGTTTG[C/T]GGTCAAGAATGCATT | 90293 |
rs776455904 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002850 | GGAAGTCCAACAAAG[A/T]TCTAATTTCCTTGAT | 90293 |
rs776461704 | snp | A/T | 2.28857e-05 | 0.00338265 | intron-variant | KLHL13 | GRCh38.p7 | X:117920222 | TGTGGTTTCAGAGTT[A/T]TAAAAGGCAAACTAC | 90293 |
rs776486649 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118043305 | ATGAATTTTACCAAA[A/C]CTTTCCAGAAGAAAT | 90293 |
rs776488456 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014657 | GATATCACAGAACCT[A/G]ACGATATGTGACTTC | 90293 |
rs776488473 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118021464 | CTCATTGTTCAATTC[C/G]CACCTATGAGTGAGA | 90293 |
rs776489980 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117921585 | TGCTTTCTAATAATA[C/T]AATACAGTAAGAACC | 90293 |
rs776497427 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118037802 | TGGGGATGGAAGAGA[G/T]ATAGACTAGATATCT | 90293 |
rs776510845 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117903184 | GAGAGGAGAGCGAGA[A/G]AGAGAGAGAGAGAGA | 90293 |
rs776511803 | snp | C/G | 4.94218e-05 | 0.00497076 | missense | KLHL13 | GRCh38.p7 | X:117910059 | AGATTGTAGGTGTTG[C/G]CAATCCGTCCAACTT | 90293 |
rs776518113 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118059598 | CAAATTTTATCTAAA[C/T]CTTCAATACCAGTAG | 90293 |
rs776528701 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118068931 | ATCCCCTCAGGCAGA[A/G]TTGAGGCTGCGCAGT | 90293 |
rs776528935 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117996127 | TTTCAAAAAAGCACA[C/G]GATTGAAAGGTTTCA | 90293 |
rs776538553 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927030 | CCTGCCTCAGCCTCC[C/G]GAGTAGCTGGGACTA | 90293 |
rs776545545 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118075749 | ATCAAAGCACTGTGT[G/T]CCATCCAAGTTATCT | 90293 |
rs776559163 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118024534 | TGAACTAAAACCTCC[A/T]AATAATCAAAATAAA | 90293 |
rs776578481 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117965117 | CAGTAATGGGATGGG[G/T]GGGTCAAATGGTATT | 90293 |
rs776601787 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117950204 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 90293 |
rs776612934 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117923746 | CCATTCAAACTGCTT[C/G]TGGAGGTATGTAATC | 90293 |
rs776622077 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978486 | GGTAATGGCTGGCTG[C/T]AAGGGGAAAGGAAAG | 90293 |
rs776626572 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038907 | ACTCCTTCCTTCCAC[C/T]TGAGGACAGAAGGGA | 90293 |
rs776628870 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118058698 | ACTTTCCAATAATAA[C/T]CAATTGCAAAATGTC | 90293 |
rs776631970 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117918218 | ATTAGTTCAAATTTT[A/G]TAAGTAATTGTGAGA | 90293 |
rs776638123 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108513 | ATTCCTCCAATGCTC[C/T]GCTGGCCTATTTTCA | 90293 |
rs776648279 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088243 | TTCAAAGAATGTAAA[A/G]CAATACCCTGTGCCA | 90293 |
rs776648940 | in-del | -/ATTC | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018517 | ACATTTCTTTCAGAT[-/ATTC]ATTAACTTATTGAAG | 90293 |
rs776657016 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941296 | ATATTGGCCTGAAAT[C/T]TTCTTTTTTTGTTGT | 90293 |
rs776659524 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117949905 | CTGGTACATTAATGT[C/G]TAGCTCACATCAAAT | 90293 |
rs776662497 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118036753 | CAAATGGGATCTAAT[G/T]CAACTAAAGAACTTC | 90293 |
rs776667780 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906788 | TACAAATCTATGAGG[C/T]CATTATAGATTTGTA | 90293 |
rs776696825 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118093688 | CATCTAAATTAATTT[G/T]GTAACTTATTAGTAC | 90293 |
rs776702484 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117957445 | TTTAATGACAACAGA[A/G]CAAACGAAAATCCAA | 90293 |
rs776702920 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117965569 | TGAGGCCAGCATCAT[C/T]CTGATACCAAAGTCC | 90293 |
rs776725961 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109979 | AGGGGTTCAACACCA[C/G]CCTGGGCAACATAGT | 90293 |
rs776726392 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118050218 | GATCCCTTGGTAGTC[C/T]CTTCTCATGTTGTCA | 90293 |
rs776737493 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117972579 | ATGATGAAGTGTGGG[C/T]ATGCCAACATCTTTA | 90293 |
rs776744818 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117969561 | GTTGAACAGAGTGCA[A/T]AGCAAACACATGTCA | 90293 |
rs776757863 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117958466 | ATCATGCATAAGGGA[C/T]AACTACTATATTCAA | 90293 |
rs776787107 | in-del | -/TTC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118067461 | TAAAAAAATTTCTCT[-/TTC]TTCAATAATAACCTT | 90293 |
rs776802482 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073860 | TCACCCTCGTATCTG[C/T]CAGGGAGGTCACTCT | 90293 |
rs776812082 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041510 | CTACAGCCTGGATGA[C/T]AGAGTGAGACCCTAT | 90293 |
rs776814043 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118051242 | TGTATGAAAGACATA[C/T]GAAAAATAAAATTTA | 90293 |
rs776826781 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118092392 | GCCATAAAGAAGAGA[C/T]ACAAAGGATTTTTCA | 90293 |
rs776831623 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117917187 | TACAATGGATTCTGA[A/G]AGGGAAGAGATTTCT | 90293 |
rs776834849 | snp | G/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118104995 | TCTGATTAGCTGTCA[G/T]TAAAAAGATTGTCAA | 90293 |
rs776852061 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118109766 | ATAGGCACTTAATAA[A/G]TATTTGTTGAATGAA | 90293 |
rs776855831 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118019529 | ATTTTGGCTTTTGTT[A/G]CCATTGCTTTTGGTG | 90293 |
rs776872568 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033810 | CAAATTGGATAAAGA[G/T]TCAAGACCCATCACT | 90293 |
rs776873250 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025559 | CTTAATAATGGCCCA[-/T]AGTGCAAGAATAGTG | 90293 |
rs776906012 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118073120 | AACCCCACAAATGAA[A/G]AAAGAAGTCCTCATT | 90293 |
rs776906608 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118042269 | AGCTGGAGACTTTAA[G/T]AACCCATTTTCAGCA | 90293 |
rs776907686 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117962640 | AAGCTTTCTAACCTC[C/T]TCCTATACCACCACC | 90293 |
rs776923190 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084492 | GAGGAAACAGGTACT[C/T]AGAGGAATAAATTGA | 90293 |
rs776923936 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097661 | AGCTGGAGGCATCAC[A/T]CTACCTGCTTCAAAC | 90293 |
rs776925927 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118105453 | CCTCATCTGTAAAGT[C/G]GGGCTAATAATAGTT | 90293 |
rs776932327 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056908 | ATTTTACTTTTTTAT[A/T]CATTTCTTTATTATC | 90293 |
rs776938968 | snp | C/G | 2.29956e-05 | 0.00339077 | missense | KLHL13 | GRCh38.p7 | X:117909960 | GCAAGACGCTCAAAA[C/G]GGAGTTTCAAGAACT | 90293 |
rs776942752 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118001192 | AACTAACTGGCATCT[A/G]GGAACCACTGCCATT | 90293 |
rs776953471 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117933520 | TATAAATAGGTTAAA[C/T]ACTTAAAAGTAAAAT | 90293 |
rs776954520 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117908407 | TAGCCCCCCAACCCC[A/T]GACAGGCCCTGGTGT | 90293 |
rs776968560 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967752 | AGGTCTTTTTAAAAA[A/G]TACACAATAGGCTTT | 90293 |
rs776974270 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118046172 | GAATGGATAAAGAAG[A/T]TGTAGTACATATACA | 90293 |
rs776976756 | snp | C/T | 0.0168099 | 0.0901243 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975177 | AGAAGGAGAAATACA[C/T]ACACACACACACACA | 90293 |
rs776978180 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118012689 | GGCGGGGGCGGGGGC[A/G]GGGGGCGGGGGTATT | 90293 |
rs776979751 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118033480 | CCAGAATTTCATATC[C/T]GGCCAAACTAAGCTT | 90293 |
rs777006995 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997576 | AAGGATGAATGTAAA[G/T]ATTCAATATGAGAAT | 90293 |
rs777022565 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118070085 | GGTTTGTAGCCTGTG[A/C]GCAACAGGCTATACC | 90293 |
rs777024064 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117992237 | GAAACTGAGATGTAA[A/T]AAAAAAAAAAAAGGT | 90293 |
rs777045413 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117997778 | GCACCCAGCACATTC[A/C]GTCTTGTCTAATAAT | 90293 |
rs777055254 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | KLHL13 | GRCh38.p7 | X:117954707 | AGGAGAAACAGCATG[G/T]GCTCCCATCACTGTC | 90293 |
rs777062303 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118067816 | TGGAATACCTTCCGA[A/T]GGACCTGCCTGAAGC | 90293 |
rs777066903 | snp | A/G | 4.60156e-05 | 0.00479642 | intron-variant, missense | KLHL13 | GRCh38.p7 | X:117972761 | AGTGGAGTTGACCTG[A/G]ATGTTTTAAGCACAG | 90293 |
rs777071238 | snp | C/T | | | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118175 | ATAATCAAAGAACTC[C/T]AAATATACATAGAAT | 90293 |
rs777081582 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089627 | GAAAGAAAGAGAAAG[-/AA]AGAAAGAAAGAAAGA | 90293 |
rs777117005 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117900209 | GACAAGGGAAAGAAG[C/T]AAGCTAATCTTTAGT | 90293 |
rs777119008 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117933395 | TTTAATAAAGGTGCC[-/A]AAGAACACACATGAG | 90293 |
rs777127590 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014303 | GGTCTATAGATGGTT[G/T]CTCTGGAAGTGTCTG | 90293 |
rs777131157 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118077476 | GGGACGTAGGGGGTG[C/T]ATTATGATTAAGGAA | 90293 |
rs777133226 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117995274 | ATAAAAAGAAGACAA[C/T]TGTAAAAATACATAC | 90293 |
rs777133864 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031175 | ATTAGGAGTTTTATG[C/G]GAAGAATTAGTTGGT | 90293 |
rs777134320 | snp | C/T | 2.30115e-05 | 0.00339194 | missense | KLHL13 | GRCh38.p7 | X:117901839 | CTTGTTTACCTGAAA[C/T]ATACATCACTCCTCC | 90293 |
rs777152642 | snp | C/T | 3.02943e-05 | 0.00389182 | intron-variant | KLHL13 | GRCh38.p7 | X:117909257 | TTTGATAAGAATTTC[C/T]GAGTGAAGAAATTTG | 90293 |
rs777154377 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118105749 | TACTGTACCTATATG[A/G]TACCAAAAGTACTTA | 90293 |
rs777154576 | snp | A/G | 2.29545e-05 | 0.00338773 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909422 | TTTATTGTATCGAGG[A/G]TCAAATCTGAAGACT | 90293 |
rs777156002 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118005590 | GAGGAAAGCAGCAGA[G/T]GTTCAAGTGAGGAGA | 90293 |
rs777178590 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088313 | GATCACTAGTTAACC[A/G]GTACTGCAATAATGT | 90293 |
rs777191382 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118054662 | ATGACATAGGCTAAT[A/G]TGAATTAAGAACCCT | 90293 |
rs777206900 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117981240 | TCATGTGTTGTAAAA[C/T]AATCACAGCTTGTTT | 90293 |
rs777239921 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925148 | CCAGACAAGCTATGA[A/G]TAATTTGTATAAAAA | 90293 |
rs777239962 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118111841 | AGGTTGCAGTGAGCC[A/G]GGATCATGCCACTGC | 90293 |
rs777245663 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006202 | GAAAGTATTTTACAT[A/G]CAAAAATGGTGGTAA | 90293 |
rs777263056 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117945971 | TAGCTACCATTTATT[A/G]AATAGTCATTATATA | 90293 |
rs777276033 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957962 | CCTTATCAGTTACAA[C/T]TTGATGAACCATGAC | 90293 |
rs777303693 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907555 | CCAAGTCACTACTTG[C/G]ACCTTCTAGATATTT | 90293 |
rs777318184 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947097 | GAGTTTCAGAGATAG[A/C]TTTAAAGAGAATTAA | 90293 |
rs777324673 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118022153 | GTCAGATGGGTAGAT[C/T]GTAAAAATTTTCTCT | 90293 |
rs777325228 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104644 | GCTCTACAGCAATTT[A/G]GAGCTAGACTGCAGA | 90293 |
rs777326970 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050491 | TAATGTTACAATTCT[G/T]ACTTATCTATAGGAG | 90293 |
rs777349191 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117902517 | GTTCGTATATACCCA[C/T]CATCATTGCAGCCAG | 90293 |
rs777353167 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118049644 | ATGCTCCCACACACG[C/T]ACCCTAACAAAATAA | 90293 |
rs777357758 | snp | A/G | 3.29728e-05 | 0.00406021 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117972864 | ATAACAGTAAAGAGC[A/G]TTTCCATAACAGACT | 90293 |
rs777373365 | in-del | -/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117969480 | GTCAGGGGCAGAGTC[-/TT]TACTAATGCAGTTTA | 90293 |
rs777378805 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000597 | TACTCAACTTTATTT[C/T]ACAAAGTAAGGACAT | 90293 |
rs777379438 | in-del | -/AAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089640 | GAAAGAAAGAAAGAA[-/AAAA]AGAAAGAAAGAAAGA | 90293 |
rs777379759 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086485 | ACACTGATTTGAATA[C/G]TTTAAAAAGGTGAAT | 90293 |
rs777395036 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118097275 | TCACAAGCATTCTTA[G/T]ACACCTATAACAGAC | 90293 |
rs777414449 | in-del | -/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117582 | AGGTTACATAAATAG[-/T]TAAGTGGCAGAGCGG | 90293 |
rs777415533 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118031730 | TATTTGAAAATTAGC[A/G]GAGGGAGCCAAGATG | 90293 |
rs777415966 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117916650 | TTTACTGATTCGCAT[C/T]TTACATACCACTGTT | 90293 |
rs777419511 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118074490 | TCCATGGATGTCCCC[A/G]CTCCTTTGGATTATG | 90293 |
rs777434429 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117978883 | CAAACCAGGATGTTT[A/G]TGTATGCTTGGGGTT | 90293 |
rs777440220 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040983 | AATATCTTTCAAACA[C/T]GAAGGAGAAATAAAG | 90293 |
rs777447547 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961396 | AACACTTTCTACAAC[A/G]CATGTGTAAGCCCAA | 90293 |
rs777450093 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064379 | GGTCAGCTTTCCCTT[C/T]TTCCCTCCAATTCCC | 90293 |
rs777478122 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118071884 | AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 90293 |
rs777478379 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000273 | TCCTAATCCATCACT[G/T]GGAATTGTGGATGGA | 90293 |
rs777481393 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978105 | TTACATTAGAAATTT[A/C]TTTAACAGAACTGTG | 90293 |
rs777488989 | in-del | -/CT | 0.495677 | 0.0462887 | intron-variant | KLHL13 | GRCh38.p7 | X:117991847 | TCTCCTACAGTGAAA[-/CT]CTCTCTCTCTCTCTC | 90293 |
rs777491522 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118096800 | AATAAACGTAATCCA[A/G]CATATAAACAGAACC | 90293 |
rs777498408 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948215 | CTAATATAGAGGAAT[C/T]TACTGTCTCATGAAA | 90293 |
rs777501242 | in-del | -/ACA | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118108296 | GATTTGAGCAGTAAC[-/ACA]ACAATATAACAATGT | 90293 |
rs777501938 | in-del | -/AGAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117998143 | GTGGGACATGAAGAT[-/AGAG]AAAGAGAGACAAATA | 90293 |
rs777510208 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118002021 | TGTCAAATTCTATCC[A/G]AACAGATACTAATGA | 90293 |
rs777510215 | snp | C/T | 4.62524e-05 | 0.00480875 | intron-variant, synonymous-codon | KLHL13 | GRCh38.p7 | X:117972748 | GTATGCTGGAGAAAG[C/T]GGAGTTGACCTGGAT | 90293 |
rs777511706 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118083479 | GAAATAAGACAAGAA[C/T]GAAAGGACAAATACC | 90293 |
rs777522506 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118040317 | GTCACATTTCAGATG[C/G]AGAATTCAAAATAGC | 90293 |
rs777531615 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033069 | AGAAATGAGCAAAGC[A/C]TCCAAGAAATGTAGG | 90293 |
rs777550514 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118053372 | GGAAACCATCATTCT[C/T]AGCAAACTATTGCAA | 90293 |
rs777555149 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991381 | GAAAAATGGTAACCA[A/G]AAATATGATTCTGTA | 90293 |
rs777562886 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959833 | AAAAGATGTTACAGG[A/G]CAACTTGTAAATGAT | 90293 |
rs777572401 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117961912 | TGATCTGAAAAAACT[C/G]TAAGATAATATGCCA | 90293 |
rs777574739 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117922267 | TCTCGGCATTGATAT[A/G]TGGGGTCTAAATTGC | 90293 |
rs777579746 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117942514 | AATGTGGGTGCTCCT[A/G]TAGTGGGTGCATATA | 90293 |
rs777590921 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118043091 | AATTCAAAGGATCAT[C/T]ACTGGCTACTATGAG | 90293 |
rs777604547 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117931548 | AGAAGACATTCTGTG[C/T]AATTCTGCTGTTTCT | 90293 |
rs777606214 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117930688 | TCCAACTTTTATCCT[A/G]AAGATGCACAGTCAA | 90293 |
rs777617693 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117941330 | TGCCAGGTTTTGGTA[A/T]CAGGATGATGCTGGC | 90293 |
rs777622988 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940108 | TAATCCATCTTAAGT[C/T]AATTTTTGTATAAGG | 90293 |
rs777634443 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944526 | GTATAAACCTTGTCC[A/C]TCATTATATTATATT | 90293 |
rs777659151 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114468 | TATGCAATCACATTA[A/G]CAGCAATCTTAGCTT | 90293 |
rs777674297 | snp | A/G | 0.0235569 | 0.105941 | intron-variant | KLHL13 | GRCh38.p7 | X:118090546 | TCATCATCACTGGCC[A/G]TCAGAGAAATGCAAA | 90293 |
rs777677673 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117992025 | CCAGGATGAGGTGGC[A/T]ATCAGTTATTCACAC | 90293 |
rs777680228 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118018325 | GAAGGTCAATGAGTA[C/G]AAGAACTCATCACTT | 90293 |
rs777707087 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118100698 | TAAATCCCTCCATTT[G/T]CTGGCCCAATTTTTC | 90293 |
rs777718944 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906593 | TAATGACTCTTTTTG[C/G]CCTTTTTTCTCCTGA | 90293 |
rs777720582 | snp | C/T | 4.56387e-05 | 0.00477674 | missense | KLHL13 | GRCh38.p7 | X:117909588 | TTTTCATCATACATG[C/T]GCAATTCCTTACTGA | 90293 |
rs777731017 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118064888 | AAAATATGTTAACTG[A/G]CTGACTAGGCAGAAA | 90293 |
rs777768112 | snp | A/G | 2.73448e-05 | 0.00369752 | intron-variant | KLHL13 | GRCh38.p7 | X:117919751 | CAATTAAATGAAGGT[A/G]GATAATTATGGTCAA | 90293 |
rs777779180 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004705 | TCAAAGTATTCTCAA[C/T]CTCATCAGAAATACT | 90293 |
rs777784663 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117990169 | TGTTACAATTGCACA[-/T]AGCATACCTAAATGG | 90293 |
rs777795248 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118101450 | AGAGAAGGAAAAACA[C/T]TACTTGTAATACAGG | 90293 |
rs777800788 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011384 | ATCTAAACAAGAAAA[C/T]AATATGACCATATTT | 90293 |
rs777806945 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030675 | TTATCATGGGAATGC[A/G]TTCCTTATAAAAGGA | 90293 |
rs777826314 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994081 | GTTTCTAATTTCAAA[A/G]GCAAATTTTGCTCTA | 90293 |
rs777867054 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118088188 | GAAATTTATTGTTAA[A/G]GCAGATAGCCTTTTC | 90293 |
rs777875450 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118023971 | GCAACTTCCCATTAT[A/T]TTCTATGTTCTGGAT | 90293 |
rs777885362 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118094963 | AAAGACCATCAAGGC[C/T]AGGAAGAAACTGCAT | 90293 |
rs777904262 | in-del | -/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117907391 | AGCCGCATATTAACA[-/G]GGGTGATAATATCAA | 90293 |
rs777905614 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021319 | TATGTATACATGTGC[C/T]ATGTTGGTTTGCTGC | 90293 |
rs777906694 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118116122 | GCACAAAGCAGAAAC[C/T]GTTAGAGGGCAAGAG | 90293 |
rs777928683 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044820 | AGACTCCAGAATATT[A/G]GTCTAGGCAAAGATT | 90293 |
rs777929389 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118044952 | AAAATGAAGAGACAA[C/T]GATAGATGGATAATT | 90293 |
rs777937770 | snp | A/C | 0.176471 | 0.238942 | intron-variant | KLHL13 | GRCh38.p7 | X:118084156 | GAAACTCTGTCTCTA[A/C]AAAAAAAAAAAAAAT | 90293 |
rs777940117 | in-del | -/AC | 0.01368 | 0.0815649 | intron-variant | KLHL13 | GRCh38.p7 | X:118069440 | AAAAAAAAAAAAAAA[-/AC]AATTTTAAAAATAGA | 90293 |
rs777953685 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118080440 | AGAAACAACCCCATT[A/T]AAAAAACGGGCAAAG | 90293 |
rs777954237 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973585 | AGAACTCTGCAGGTT[C/T]TTCTAGTAGCTTCTG | 90293 |
rs777963824 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117919426 | CACATCTGTCTAATG[C/G]CAAGTTTCACATTCC | 90293 |
rs777971722 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118095572 | GAACTCTCCACCCCA[A/G]ATCAACAGAATATAC | 90293 |
rs777973216 | in-del | -/AAA | 0.0527491 | 0.153597 | intron-variant | KLHL13 | GRCh38.p7 | X:117996831 | AATCATAGCCTATTT[-/AAA]AAAAAAAAAAAAGCT | 90293 |
rs777979314 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118025826 | TTGTGGAGAAGGAAG[A/G]AGCAGCTTGTGCTAG | 90293 |
rs777991944 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117904925 | ATTATACTTAGGTTG[A/G]TTATCTCACATATAT | 90293 |
rs777994700 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025290 | CCATGGTCAACCACA[C/T]TCTAAAGAAAATATC | 90293 |
rs778007326 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974636 | AATCACAAATGCCTT[C/G]CTTTTAAGATACAGA | 90293 |
rs778009535 | in-del | -/AG/AGAG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089628 | AAGAAAGAGAAAGAA[-/AG/AGAG]AGAAAGAAAGAAAGA | 90293 |
rs778010270 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117970049 | CTATCTGTAGCATCA[A/G]TGGAAGAGCTACAGC | 90293 |
rs778020394 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078642 | GGTGTACATACACCA[A/C]GTTTGTTTATTCTAT | 90293 |
rs778027617 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118088062 | TCACCTGCAAGAGCA[A/G]GGGAAAGCAATGCCA | 90293 |
rs778029167 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060344 | TAAATGCATATTATT[-/G]AGTATAAAGGTATTG | 90293 |
rs778036085 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039592 | GCACCAGGTAGATTC[C/G]TAAGGTTTCCGACTC | 90293 |
rs778039806 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117909017 | ATTTAAATGAGCTAA[C/G]TATACTCTTTAGATG | 90293 |
rs778059737 | snp | C/T | 2.91346e-05 | 0.0038166 | intron-variant | KLHL13 | GRCh38.p7 | X:117910139 | ACATGACTACTTTCA[C/T]GGCAATCACATCTTG | 90293 |
rs778100639 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109584 | TCTGTGTAAAACAGA[A/T]GCTTCAAGAAAATAC | 90293 |
rs778115265 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118051140 | TCCACCAATATCATA[C/T]TCTATAAGTACTGGA | 90293 |
rs778124845 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117965902 | TATTGATGGGATGTA[C/T]CTCAAAATAATAAGA | 90293 |
rs778147482 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117926998 | GCAACCTCCGCCTCC[C/T]AGGTTCACGCCCTTC | 90293 |
rs778160901 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117899818 | CACATTAAATTCCAG[A/G]TTCCCATTTCCTCAC | 90293 |
rs778169745 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113589 | ATGTTATCTCGGGAA[C/T]GTTCTCCCAGATCCT | 90293 |
rs778173415 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118105321 | TAGCATGAAAGGAAG[C/T]GTTGTGGTTAAAAGC | 90293 |
rs778183285 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118042931 | AATGAAAAAAAAAAA[A/T]ACAAAAGATCAACAA | 90293 |
rs778184684 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941757 | GGCTAGCGGTCTATC[C/T]ATTTTGTTGATCTTT | 90293 |
rs778192346 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118096243 | ACAAAATGACAAAGG[C/G]GGTATCACCACCGAT | 90293 |
rs778195811 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118032378 | AGTGGTTCTCCCAGC[A/C]CGCAGCTGGAGATCT | 90293 |
rs778219612 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117993766 | TTTTAGTTGGAGTTT[C/T]GCTCTTGTTGCCCAG | 90293 |
rs778225004 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967497 | ATTCTCAGTAACTCC[A/G]TACTTCCCATGATGG | 90293 |
rs778244187 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118092869 | CTGGGTGACAGGTAC[C/G]CAGGACCTCTCTGTA | 90293 |
rs778251861 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117936632 | CCTACCCTCACTGTT[A/C]TGCTCTGTCTAGGTG | 90293 |
rs778259611 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118114452 | ATATAAATAGTCTTA[C/T]TATGCAATCACATTA | 90293 |
rs778263665 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118008665 | GGAGAGGTGATACAG[G/T]ACAGGCAAAACCCTT | 90293 |
rs778267262 | snp | C/T | 0.085528 | 0.188279 | intron-variant | KLHL13 | GRCh38.p7 | X:118098148 | TGAACAGGCAACCTA[C/T]AGAATGGGAGAAAAT | 90293 |
rs778270858 | snp | C/T | 0.0209675 | 0.10022 | intron-variant | KLHL13 | GRCh38.p7 | X:118110383 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTG | 90293 |
rs778271673 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117951413 | AGCTTGAAAGTAACA[C/T]CTATTAATAAGGCAT | 90293 |
rs778273779 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117927589 | GGAAGATGGTCCAGG[C/T]GGAGGAGAATGAAGA | 90293 |
rs778288844 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117937994 | AATGGAATCACATAA[A/T]ACATGAAATCACATA | 90293 |
rs778293572 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117931128 | TCTTTAACATTCTAT[C/T]AGCTAGAGGATAAGA | 90293 |
rs778298009 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118042099 | TCAAGACAAAAACTA[C/T]AAAGAGACAAAATGG | 90293 |
rs778307157 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117942677 | TTTTGTTTTCCATTT[G/T]CTTGGTAAATATTCT | 90293 |
rs778318071 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118056283 | TATATTCTGGCAACT[A/G]TAAAACATTGCTGAA | 90293 |
rs778318221 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005670 | GAGACACAAGCAAAG[A/G]CACATAGGTGGCCTC | 90293 |
rs778332801 | in-del | -/AAAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011077 | ACACTGTCTCAAAAT[-/AAAT]AAATAAATAAATAAA | 90293 |
rs778334415 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117901427 | AAATTTACAGAATGC[C/T]CAAGACATTCATATG | 90293 |
rs778334829 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117970988 | ATGCAAGATCTATTA[C/T]ATTTTGTAGGTTCTA | 90293 |
rs778340540 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-5-prime, intron-variant | KLHL13 | GRCh38.p7 | X:117985404 | CTGCCTGGTACAACA[C/T]TTCAGTTGTAGCTCC | 90293 |
rs778346337 | snp | A/C | 1.64751e-05 | 0.00287007 | intron-variant | KLHL13 | GRCh38.p7 | X:117972715 | CCACTTTAATATCCT[A/C]TTTTCTCTCACTTAC | 90293 |
rs778348696 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118005483 | CATATGTTGCCTAAC[A/T]TAGCAAGAGATGATG | 90293 |
rs778349439 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118106119 | TTTCACCATGGTCTC[A/G]ATCTCCTGACCTCGT | 90293 |
rs778357726 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080159 | AATTTAAGAACTCAA[A/T]CTATAAAAAGTGTAG | 90293 |
rs778364536 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118020100 | GTATGGTCATTTTCA[C/T]GATATTGATTCTTCC | 90293 |
rs778366483 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013123 | AAACAAGTTGAACAA[G/T]ATGCCTGGCCTCTTG | 90293 |
rs778367165 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118069712 | GAGGCAAAAAGTTTT[A/T]AAAAATTAAAAAGTG | 90293 |
rs778374748 | in-del | -/AG | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089619 | GAGAGAGAGAAAGAA[-/AG]AGAAAGAAAGAAAGA | 90293 |
rs778397917 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917794 | GTTAATGATTAGTTC[C/G]AAAGAAATCATGGCA | 90293 |
rs778400528 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117984044 | GTTCTTCTAGGTTCA[C/T]TTACTACCAATTCTT | 90293 |
rs778446229 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085286 | GCCAGACACAATAGG[A/C]CATTTATTGTATTAT | 90293 |
rs778454625 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118013755 | GGAAGTCAGAGACCC[C/T]GAACGGAGAGACCGG | 90293 |
rs778472641 | in-del | -/A | | | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:117973117 | AGGACTGCACTGTGC[-/A]TACCATACAATGCAG | 90293 |
rs778481865 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117900172 | GTCTCTACAATGAAA[A/G]TATTAAACGATACCT | 90293 |
rs778498720 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074673 | TGTGCCCATAATTAT[C/T]ATCTACATTTGAAAA | 90293 |
rs778503518 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975498 | CAGGTTGCAGCAATT[C/T]TCCTGCCTCAGCCTC | 90293 |
rs778519670 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118056253 | AAATAAATTTAACAG[-/A]AAAAGTACAAAATTT | 90293 |
rs778544515 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117997512 | AAAAATCTGTCTTCA[A/T]GCAAAATATTTTGAA | 90293 |
rs778557853 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118111272 | CATTAGGGTCTATGG[C/T]GCAACCCCATAAACA | 90293 |
rs778563638 | snp | C/T | 0.116289 | 0.211238 | intron-variant | KLHL13 | GRCh38.p7 | X:118036187 | GGTAATTTACAGATT[C/T]AATGCCATCCCCATC | 90293 |
rs778578580 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118113235 | TAGCATACTGATCAT[-/A]AGAGTTTTTTTTATT | 90293 |
rs778587553 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118048545 | ATGGTGGCTACATGG[A/G]CAACTGTTATATTGT | 90293 |
rs778588679 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118067045 | AATGTGTCATTAGGT[A/G]ATTTCATCATTATGC | 90293 |
rs778594208 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985848 | CCCAGGAATCTAGCC[C/T]CTACTGTTTTTTTTA | 90293 |
rs778606120 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118071231 | TACGTGTGCATGTGT[C/G]TTTATAGCGGCATGA | 90293 |
rs778606587 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118057344 | TTTGTGTATACCATA[C/T]ACAAATATTAACTAA | 90293 |
rs778611312 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118048299 | AAGTAAACAAGTACA[C/T]ATATGTACACACATA | 90293 |
rs778626168 | in-del | -/TGT | 0.0100156 | 0.0700533 | intron-variant | KLHL13 | GRCh38.p7 | X:117976983 | AGCTAACTTGCCCAA[-/TGT]TGTATCACAAGCTAG | 90293 |
rs778634027 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967260 | TCTCATGTTTATACC[A/G]CCTTTCTCAAAGTCT | 90293 |
rs778639950 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030357 | ATTTTTTAATTATGT[C/T]TAGACTATACAATTA | 90293 |
rs778644308 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118082038 | GTTAGGTTGATTTCA[C/T]ATCCTGGCTATTGTG | 90293 |
rs778649979 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117946954 | ATGATATTAGAGCCA[C/T]AGTATAACCAAAAAT | 90293 |
rs778658546 | snp | C/T | 2.31043e-05 | 0.00339877 | missense | KLHL13 | GRCh38.p7 | X:117909401 | TAAAGATGCAACTTG[C/T]ATCCATTTATTGTAT | 90293 |
rs778673686 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117940007 | TGTGTTAGTCATCAA[C/G]TCTTTGCCGATGCCT | 90293 |
rs778674290 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117946297 | TTCCATCTTTTCAAA[C/G]AAATGAATACTAAAA | 90293 |
rs778694518 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118047777 | GATGGGAGAGATGTT[G/T]ACTTTTAATCCTGTA | 90293 |
rs778697469 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039432 | AGCCTTGAGTGAACA[C/T]CACTGGTAGCTAGAT | 90293 |
rs778702740 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117959697 | TTCTAAGGTTCCTAT[C/G]AGCTTGTGGATTGAA | 90293 |
rs778703312 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968367 | ATGGAATGAGTTCCT[C/G]TGTTAAAAGGGGTTT | 90293 |
rs778703577 | in-del | -/GATA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076954 | CAACCCCCACCCCTT[-/GATA]GATAATCTCCTAATG | 90293 |
rs778706110 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117961224 | AATTCCACTTTTTAA[C/T]AAGATTTCCAGGAAA | 90293 |
rs778708930 | snp | C/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:117998755 | TGTCTCTGGGGGCAC[C/G]ATGAGAAGCTACTGA | 90293 |
rs778718370 | snp | A/C | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:118010850 | GGCTGAGGTGGGTGA[A/C]TCACTTGAGCCCAGG | 90293 |
rs778729631 | snp | A/C | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:118103032 | ACAGGTTTCTAATGT[A/C]TTTTAACATAGCCCA | 90293 |
rs778729908 | snp | A/T | 0.00158814 | 0.0281345 | | | GRCh38.p7 | X:118022640 | TTATGTATTATTTTT[A/T]AAAATATATCTATTC | 90293 |
rs778731743 | snp | G/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:118031036 | CTCCTGAGGAGCAGG[G/T]AGTAGGTGATAGGAT | 90293 |
rs778745678 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:117939331 | CATTTTGTTTATCCA[A/G]TCTATCATTGATGGG | 90293 |
rs778757557 | snp | A/C | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:117952233 | GGAACAGAACAGAGC[A/C]CTCAGAAATAATGCC | 90293 |
rs778758981 | snp | C/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:118116280 | CCCAGGCGTCCGACG[C/G]AGCCAGAGGGACCGG | 90293 |
rs778765939 | in-del | -/AGAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903190 | GAGCGAGAGAGAGAG[-/AGAA]AGAGAGAGAGAGAGA | 90293 |
rs778772836 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947667 | CTGAAGAAGCCTGGA[A/C]TAAAATTATCTTTTT | 90293 |
rs778781549 | snp | A/G | 2.54891e-05 | 0.00356986 | intron-variant | KLHL13 | GRCh38.p7 | X:117901965 | TTAAAAAAAAAAAGA[A/G]AAGAAAATTATTTTT | 90293 |
rs778789872 | in-del | -/AAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117962042 | GACCTCATCTCTACA[-/AAT]AATAATAATAATAAT | 90293 |
rs778817753 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118096335 | AAAATCTAGAAGAAA[A/T]GGATAAATTCCTCGA | 90293 |
rs778818791 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117906373 | ACACGATCATGGATA[G/T]AATTCAGGAAATTTC | 90293 |
rs778819698 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118103709 | GTAGCTTATTACTTT[A/G]ATGAAGACCTGGGAA | 90293 |
rs778837798 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011253 | GCAATATGAGGGAAC[A/G]GGTCATCTTCCAGTG | 90293 |
rs778848601 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117906445 | TTCATCAAGTTTGGT[C/T]ACCTCCGTAATACAG | 90293 |
rs778849041 | snp | C/T | 0.00158814 | 0.0281345 | utr-variant-5-prime, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117287 | CTCACCTCAGTGGGG[C/T]CCACGTCTCAAAATA | 90293 |
rs778863956 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117929717 | GAGGTTGAGGCAGGA[A/G]GATTGCTTGAGCCCA | 90293 |
rs778873524 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033029 | AATGAAGTGAGAAGG[A/G]AAGTTTAGAGAAAAA | 90293 |
rs778875213 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118104454 | GCCACTCATACTAGT[C/G]GGTTTAGCAGTTTTG | 90293 |
rs778883697 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914336 | AAACACCACTGCACT[C/T]GGACCAGCCAGTATC | 90293 |
rs778886538 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | KLHL13 | GRCh38.p7 | X:118071667 | TACAAAAATCACAAG[C/T]ATTCTTATACACCAA | 90293 |
rs778901349 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117907382 | AAGCTAAGTAGCCGC[A/C]TATTAACAGGGGTGA | 90293 |
rs778904200 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117972132 | GAATACTTTTTCAAT[A/C]CCCATAATATAACTG | 90293 |
rs778904481 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083577 | TTATCAGAGGCTGGG[A/C]GAGAGTGGGGGGCAG | 90293 |
rs778910269 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118002600 | CTCTGTCTCGAAAAT[A/C]AATAAATAAATAAAT | 90293 |
rs778915560 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117990187 | CATACCTAAATGGCT[A/C]CTTTTGATGTTTGCA | 90293 |
rs778917106 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118090336 | AAAAGAGTGAACAGG[A/C]AACCTACAGAATGGG | 90293 |
rs778924946 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118100572 | AATATGCCAGTTTCA[C/T]GACCCATTCAGCCTT | 90293 |
rs778950644 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118050255 | ATAGGCTTTAGGAAT[A/G]CCTTTGAGGTATATT | 90293 |
rs778951093 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117921284 | TTATTTTTAATTTTT[A/G]TGGGTACAGAGATGT | 90293 |
rs778952365 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118028199 | CATAATTTATACCAA[C/T]TACATTTTCTAAATA | 90293 |
rs778968724 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117991270 | AAAAGCTTCTAGGAG[C/G]ATATTAATCCTGAAG | 90293 |
rs778984455 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118013015 | AGCACAGACAGAGGG[G/T]AAATGGTTAATTCCT | 90293 |
rs779005298 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118082949 | TATATTCTGTTCTAG[C/T]GGTCTATGTGTCTGT | 90293 |
rs779008324 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117922091 | TTATTTAGAAAAGTA[G/T]AAGTAAAATAATAAT | 90293 |
rs779015152 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094364 | ACAAAGAAATGAACA[A/C]AGCCTTCAAGAAATA | 90293 |
rs779031717 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118011664 | GTCCAGGATGATGCC[C/T]GAGTTTCTGAGTCAG | 90293 |
rs779037623 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117991452 | ATTTCTAATTCAAAA[C/T]TTAGAATTCATTTTG | 90293 |
rs779047401 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118036638 | CCAAAACCATAAAAA[C/G]CCTAGAAGAAAACAT | 90293 |
rs779050791 | in-del | -/C | 0.00422943 | 0.0457911 | intron-variant | KLHL13 | GRCh38.p7 | X:118052674 | CTACTAAAAAAAAAA[-/C]AAAATACAAAAAATT | 90293 |
rs779076835 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094140 | GAAGTTAAAAACCTT[C/G]AAAAAAAATTAGATG | 90293 |
rs779086913 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118044607 | AATGAACTCATTTTT[C/T]ACAAAGGTGCCAAGA | 90293 |
rs779088594 | snp | G/T | 2.28995e-05 | 0.00338367 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117909896 | ACAGGTAGCCTTAAA[G/T]AGCTCAAGTTCAGTA | 90293 |
rs779094342 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118076313 | ATGTAACAAAACTCA[A/C]CAATCACAAGATAAA | 90293 |
rs779095698 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117981666 | CACTACAGGGTCTAG[C/G]CATTTGTTTAAATTT | 90293 |
rs779098935 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117936448 | CTCAAGCCAACCAGA[C/T]GGACACCTTATTCGG | 90293 |
rs779113053 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118061171 | AATCATAAATAAAAT[C/T]TGTGGAGGTTGTTTT | 90293 |
rs779123393 | in-del | -/CTCT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027620 | ACTCACTCACACCCG[-/CTCT]CTATTTTTTCTCTCT | 90293 |
rs779126279 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118114230 | GCAAGTCAAATTACA[A/T]GAAGAAGCATAATTT | 90293 |
rs779130276 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912782 | GGCACATAGTTGGTA[G/T]ATATATTTATGGGGT | 90293 |
rs779136198 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118078480 | AATTTTGCCTTTCCC[A/T]GAATGTCATATAAAT | 90293 |
rs779137238 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118020705 | CACGTATGTTTATTG[C/T]GGCACTACTCACAAT | 90293 |
rs779138838 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118053286 | AAAATGTGGCACATA[C/T]ACACCACGGAATACT | 90293 |
rs779139508 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970402 | TATATATCACGATTT[A/C]TTGAGGAGTCAGAAT | 90293 |
rs779141337 | in-del | -/GAAAA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117930813 | TGCCATTCAGGAAAT[-/GAAAA]GAAATTAAAAGTATC | 90293 |
rs779148137 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118108173 | AAACTCTACAAACTA[A/C]AAGCAAAACTCTTAT | 90293 |
rs779150313 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917654 | GTAATATTACTATAA[A/C]TTTTTTGTATTGTGT | 90293 |
rs779157030 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117943583 | CATTAAGTTGATCTT[C/T]AATCTCTGATATCCT | 90293 |
rs779159996 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117957085 | CACCTTTGACCCTTG[A/C]TTCTTCCCCATTTCC | 90293 |
rs779178703 | snp | A/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:117996796 | TAGCACGCACATAAT[A/T]CTTCAGAAAACACTG | 90293 |
rs779178953 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916720 | ACACAAATGATTGAG[-/A]ATAGGATAGAACAGA | 90293 |
rs779184546 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:118069361 | ATCCTAACCCTGTGT[A/T]GGCCCAGGCTGATGT | 90293 |
rs779201479 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117978315 | ATGGCATAAGCAATG[A/T]GAAGGGCAGTAATTC | 90293 |
rs779203941 | snp | C/G | 2.29637e-05 | 0.00338841 | missense | KLHL13 | GRCh38.p7 | X:117899328 | CATTGGCGCCTTCTG[C/G]ATCCATTTGTCAGTA | 90293 |
rs779215848 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113446 | CCTATTTATCGGTTA[C/T]TGAGCTGCTTCTAGG | 90293 |
rs779242513 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100601 | TTCAACCCAGCCCAC[C/T]TATCAGTCAGATACA | 90293 |
rs779243660 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118055574 | GTAAAGTAAGTGAGG[C/G]TCTCACCTCAACCAC | 90293 |
rs779265029 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118060175 | GAGGAAGAATACTTA[G/T]CTCAGCATATTCCCA | 90293 |
rs779273520 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921900 | ATTTATACATTATAC[A/G]TACACTTTAAAACAA | 90293 |
rs779290157 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916327 | AAGTGGTTTTAGTTT[C/T]ACAGAAATTTTTACC | 90293 |
rs779294705 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118094856 | GAGAGATTTTGTCAC[A/C]ACCAGGCCTGCCCTA | 90293 |
rs779298900 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030977 | CTGGATTTCTGAGTC[C/T]GGGATATTCTTATTC | 90293 |
rs779303687 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118105161 | TTGCTTTTCAATAAG[A/C]CCTCCTTTAAAAGTG | 90293 |
rs779304347 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118014485 | CAATGCATGCACAGC[A/G]GCACACAGACCCTCA | 90293 |
rs779322614 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112665 | AAATCAAGTTGACCC[C/T]GCAGGCACTGATGAA | 90293 |
rs779336012 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117949984 | CTTTCCTGTACTGTT[G/T]GTAATTTCTGAAGGG | 90293 |
rs779354696 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118050928 | CAGTTGGTGTGGGAT[A/C]GGTCTAGAGAATCTG | 90293 |
rs779369013 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000981 | ACAGTCCTTGATTAA[C/T]ATCGTAAATTTAATT | 90293 |
rs779377264 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118073044 | GGCTTCAGCGAACCA[A/C]GACTGTGCCACTGCA | 90293 |
rs779381626 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118086662 | TTGTGTTTAAAAGAG[G/T]ATATACACACATGCT | 90293 |
rs779388105 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117937932 | GTAAGCAACCAATAG[C/T]CTACTTTACGTCTAT | 90293 |
rs779407208 | snp | C/T | 0.0115877 | 0.0752302 | intron-variant | KLHL13 | GRCh38.p7 | X:118097484 | AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 90293 |
rs779414803 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076676 | TCCTTCCTAATGTTG[A/G]TGAGTCTCATCCAAT | 90293 |
rs779418670 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118118836 | TTTATGTGCTATGTG[A/G]CATTAAGTTAGTGCT | 90293 |
rs779444523 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978815 | TTTTTTTTTCTACCC[A/G]TGTATGCTTCAAAGT | 90293 |
rs779463729 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118065414 | AGGCAAACATGGGTT[A/G]TTCTTTCCAATCTAA | 90293 |
rs779464358 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950710 | CCACTACCCAACCCC[C/T]AGGAAAATAAAATAC | 90293 |
rs779479984 | snp | A/G | 0.000159606 | 0.00893183 | missense | KLHL13 | GRCh38.p7 | X:117909774 | CTCATGAAATCCACC[A/G]TTTGCACGTAATTAA | 90293 |
rs779481173 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117983965 | TTGCTGATATACTTC[C/T]TTGCCATAAAAACCT | 90293 |
rs779482997 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007861 | GCTATTAATAAGTCC[A/C]AAAGACAGGCATGGA | 90293 |
rs779487897 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118012669 | ATTAAAATGTGGCCA[C/T]CCTGGGCGGGGGCGG | 90293 |
rs779491749 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117917649 | TGACAGTAATATTAC[G/T]ATAACTTTTTTGTAT | 90293 |
rs779500076 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118000431 | CAATGTATTTCCTTG[A/C]AAACAAAATAGAGAG | 90293 |
rs779507041 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097943 | TCAAGATGGATTAAA[C/G]ACTTAAACGTTAGAC | 90293 |
rs779507046 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025975 | GATGACAGTTGGATT[C/T]GGTACTATCCTCAGT | 90293 |
rs779514333 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117934015 | TGGGGGCCATTATCC[A/C]AAGCAAATTAAGGCA | 90293 |
rs779540987 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117941089 | GTGGGTTTGTCATAA[A/T]TAACACTTATTATTT | 90293 |
rs779541497 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117962368 | TGGGAGGATAATGTC[C/T]GCAGGAAAGTACTAA | 90293 |
rs779552807 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117992145 | CTTTTAGAGCCCTAG[C/T]AACTTTGGATGGGGT | 90293 |
rs779559706 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117954420 | GACGGATGGATGGAT[G/T]GATGGATGGATAAAG | 90293 |
rs779569060 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004318 | AGCTCTCTCCATCAA[A/G]AGGGCCTTGGAACAG | 90293 |
rs779586573 | snp | A/T | 0.00964608 | 0.0687749 | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898186 | GTGCCACTCAATTTT[A/T]AAAAAAATTATATTT | 90293 |
rs779628024 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041363 | AAAACCCTGTCTCTA[-/C]AAAAAACACAAAAAC | 90293 |
rs779656804 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117983640 | ACAGCATTTTAGCTG[A/T]AAATTAATAAACCAT | 90293 |
rs779664606 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118085194 | CCTTGTAGAATTATT[C/T]ATCCATAGAAAGAAG | 90293 |
rs779684199 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994807 | CCAGGCACAGTGGCT[A/C]ACGCCTGTAATCCCA | 90293 |
rs779685264 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118092792 | ACACACATTGTACCA[A/C]TATCAATTTCTGGGC | 90293 |
rs779710492 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087514 | CAGACATAATCATCC[A/G]CATTTTTATCCCGAG | 90293 |
rs779712512 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:117970926 | TAAGCTCTTTGAATA[C/T]ATTTTTCCATTCTAC | 90293 |
rs779735561 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118066111 | TCCAATTCAGGAAGA[C/T]AGTTAAGCCAGTATG | 90293 |
rs779750304 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118006080 | GACTGGGTTGAGTTT[C/T]CATTCTATTTTTATC | 90293 |
rs779762119 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118084305 | CCTGGATGACAGAGT[A/G]AGACCCTGTCTCAAA | 90293 |
rs779763423 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118068683 | AGATAAGAAGCCAAC[A/G]CTGTGCCCCACCCCA | 90293 |
rs779767277 | snp | G/T | 2.58428e-05 | 0.00359454 | intron-variant | KLHL13 | GRCh38.p7 | X:117972686 | TGCCACAAGGTAGAT[G/T]CATGAATGAAATCCC | 90293 |
rs779768298 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015661 | AATATATAAAACATG[C/T]AACATTACTAACAAG | 90293 |
rs779772784 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118095783 | GAACAACCTGCTCCT[G/T]AATTACTACTGGGTA | 90293 |
rs779780568 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117967329 | TCTAAAATTTTATCA[G/T]GTATGTTGTTTGTAA | 90293 |
rs779783479 | snp | G/T | 0.000178333 | 0.00944111 | intron-variant | KLHL13 | GRCh38.p7 | X:117985198 | TTGCTATTTTAATGA[G/T]TAAGTAACAGCAGTA | 90293 |
rs779783656 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974808 | CTTTGTAAATATTAA[A/G]ATTATGTCAGCCATC | 90293 |
rs779791128 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117947582 | CTTAAAAACAGAAAG[C/T]AAAAAGTGAAAATGC | 90293 |
rs779793285 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118022585 | ACATCTCCCTGATGA[C/T]GTGATGTTGAGCACC | 90293 |
rs779803249 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118038590 | CTCAGCCAACGACCA[C/T]GGAGGGAGCATTTAG | 90293 |
rs779817730 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118046464 | GATAGAATAAATAAG[A/T]TCTATTATTTGATAG | 90293 |
rs779818056 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118102714 | CGAATCTTCTTTATG[C/T]GCAGATAAAGCAGAT | 90293 |
rs779824711 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985636 | TTTGGAGCAAAGGTG[C/G]AGTGAGACAAATACT | 90293 |
rs779826544 | snp | G/T | 2.29845e-05 | 0.00338995 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117901942 | ATTGTAACATTCTAC[G/T]GTGGCTGTTAAAAAA | 90293 |
rs779836356 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117996848 | AAAAAAAAAAAAAGC[C/T]ACATGTGCTATGCTC | 90293 |
rs779836445 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117975371 | AAGAGACTCAATCAT[A/T]TTCCAGCTTATGAAT | 90293 |
rs779843135 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117963754 | GACTTTTTAATGATT[A/G]CCATTCTAACTGGTG | 90293 |
rs779846067 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118005220 | CCACAGATAACAACA[G/T]ATGACTGTATATATA | 90293 |
rs779851428 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916179 | CAAAACAAACAAACA[-/A]AAAAAAAAAACACTA | 90293 |
rs779859408 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117923617 | TACAATTGGAATTGA[A/G]TAATGTCAGTATGTT | 90293 |
rs779879899 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118110232 | TTTTAATCTTAATGA[C/T]GTCAAGTTTACAGAG | 90293 |
rs779884594 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047985 | TAAGGAAGTGAGAAA[C/T]GACAACTTAGTGTAG | 90293 |
rs779891046 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118021900 | CCTCTCCAGCACCTG[C/T]TGTTTCCTGACTTTA | 90293 |
rs779905485 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117960126 | CTCATGTCTGTAATC[C/T]CAGCACTTTGCGGGG | 90293 |
rs779906531 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118035319 | GACCAATATCCTTGA[A/T]GAACATTGATGCAAA | 90293 |
rs779913045 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117966178 | CTCAGCCCAAAATCT[C/T]CTTCAGCAAAGTCTC | 90293 |
rs779914744 | snp | A/G | | | missense | KLHL13 | GRCh38.p7 | X:117899161 | TGCCCTCTTAACATG[A/G]CAGCAATTGGGGTCC | 90293 |
rs779921568 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117946664 | AGGAAAAAAGAAGGA[A/G]AGCAGATTTTCAAGT | 90293 |
rs779923691 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080577 | ACCCTCTTACACCAG[A/T]GAGAATGGCTGTTAT | 90293 |
rs779965681 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102143 | GGACTTGTATACTCT[A/G]CTGAGAAGTCTTAAT | 90293 |
rs779982743 | in-del | -/TAAT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117914660 | AAAGGGATAATTGAA[-/TAAT]TAATAAACACCTCTC | 90293 |
rs779987416 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118061313 | GAAACCACGAGCATT[C/T]GGTGGGCAGAGGTAA | 90293 |
rs779997869 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118016916 | GTTCCCAAACATTGT[A/G]AAATTCATCCCTAAG | 90293 |
rs780000244 | snp | A/T | 2.30314e-05 | 0.0033934 | missense | KLHL13 | GRCh38.p7 | X:117945521 | GGATGAGAGGCCCAT[A/T]TCGCTGCCTCCAAGG | 90293 |
rs780014323 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117910715 | TTATTTATCTGGAAA[C/T]ATAAGCAAGGAAATG | 90293 |
rs780030064 | in-del | -/ACA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117997226 | TAGAAGCCTACTGAC[-/ACA]ACACTCTCTTATGGA | 90293 |
rs780030869 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117928264 | AGATTTCAATACCAT[C/T]CTCTCAATAATTGAT | 90293 |
rs780039310 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117914758 | AGCCCAAAATATTCA[A/T]TTCTCTATTTATTTG | 90293 |
rs780046790 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118090306 | AAGAGCTTCTGCACA[A/G]CAAAAGAAACTACCA | 90293 |
rs780053917 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118102736 | AAAGCAGATCCCCAT[A/G]TAAAACAGGTAGATG | 90293 |
rs780058839 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968827 | AGGGGATAGAAACAT[A/G]TCAAATTTAGAAAAT | 90293 |
rs780060497 | in-del | -/GA | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903180 | GAGAGAGAGGAGAGC[-/GA]GAGAGAGAGAGAGAG | 90293 |
rs780069069 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107418 | CAGCTAGGATTAAGA[A/C]AATATAAACAAAGAA | 90293 |
rs780076723 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118033001 | TATCAGCGACGGAAG[A/C]TGAAATGAATGAAAT | 90293 |
rs780077819 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118039346 | TGCCCTGGCCAGAGG[G/T]GAGCCCACTGCCCTG | 90293 |
rs780085329 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117929589 | GCTAAGATCATTTCT[G/T]AATGACTACAGAAAA | 90293 |
rs780089340 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118116107 | GAGATGGATTAGGAG[A/G]CACAAAGCAGAAACT | 90293 |
rs780090283 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117967806 | GCACATGCCAGGCTT[-/C]CTCAGACTAAAAGAT | 90293 |
rs780110243 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117904257 | TCTCCATGCAGAGTT[A/G]CTATTGTTATCAGTA | 90293 |
rs780115275 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118052600 | TGGGAGGCCGAGGTG[A/G]GCAGATCATGAGGTC | 90293 |
rs780118506 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117907174 | TCCTGTGTATGAGCC[A/G]CTTGCCCAACAGTGT | 90293 |
rs780130142 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070791 | TTTAAGTTTTAGGGT[A/T]CATGTGCACAATGTG | 90293 |
rs780146766 | in-del | -/TCC | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081689 | AACACTAGAACTTAT[-/TCC]TCCTATTTAACTGTA | 90293 |
rs780153973 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118099672 | TTTTAAAAAAAATTA[G/T]CTGGGCATGGTGGCA | 90293 |
rs780155846 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117920975 | TTGTTTGAAAAAAAA[A/C]AAAAAAAAGCCCAGG | 90293 |
rs780161409 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118106406 | TATTTAAGGTTTGAG[C/T]TAATGACCTAATGGT | 90293 |
rs780165696 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032723 | TTCCTCACCAGCAAC[A/G]GAACAAAGCTGGACG | 90293 |
rs780185965 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112577 | AAAGTTCCAAACTGG[A/G]GAAAATCAGTTTAAA | 90293 |
rs780186283 | snp | A/C | 0.000121797 | 0.00780279 | synonymous-codon | KLHL13 | GRCh38.p7 | X:117898911 | GTAGAGATGATCTTA[A/C]GGTGCAGAAAGAGGG | 90293 |
rs780188089 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117922979 | TACATACTGTTGTGC[A/C]TTTTAAAATTCACTT | 90293 |
rs780210867 | in-del | -/AACA | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118052002 | TGGTACTAGTGTGGG[-/AACA]GACAGAGGAATGAAC | 90293 |
rs780219506 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118071218 | GCCGCAATAAACATA[C/T]GTGTGCATGTGTCTT | 90293 |
rs780220256 | snp | A/G | 0.000162933 | 0.0090244 | intron-variant | KLHL13 | GRCh38.p7 | X:118028391 | ATAAATAGGAAAGAC[A/G]TTATATAAGTTAAAC | 90293 |
rs780225126 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118063262 | TGTACTTTAGAGGAG[C/T]GGAAAAAGGGAATCA | 90293 |
rs780225633 | snp | A/T | 2.58829e-05 | 0.00359733 | intron-variant | KLHL13 | GRCh38.p7 | X:117919735 | TAAATAAAAAGACAT[A/T]CAATTAAATGAAGGT | 90293 |
rs780252015 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118082795 | AGAGATAAGGGTCTA[-/C]TTTTCATTTTTCTGC | 90293 |
rs780260491 | snp | A/T | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117987276 | ACCCAAAGATCCATA[A/T]AATAAACAAAAGGAA | 90293 |
rs780262075 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118009047 | AATATAAGAGTCAAT[A/G]CTATTGAGAAGTGTC | 90293 |
rs780279815 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | KLHL13 | GRCh38.p7 | X:117911748 | CCTTTTTTATGGCTG[C/G]ATAGTATTCCATGGT | 90293 |
rs780280428 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117920097 | TTAAAACAGCACCAC[C/T]GAAAACCATACATAC | 90293 |
rs780305651 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118063101 | GGGATGATCTAAATA[A/G]ATATGCAGAGAGACT | 90293 |
rs780319107 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971761 | AACAAAAACTAAGTT[-/A]AAAAATGGCAACTCA | 90293 |
rs780321373 | in-del | -/TA | 2.47957e-05 | 0.00352097 | intron-variant | KLHL13 | GRCh38.p7 | X:117901797 | ATATAGTTAAAAGCT[-/TA]TATATTATATTGTGT | 90293 |
rs780321703 | in-del | -/ATC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118109138 | CTCTATTCTGAAAAT[-/ATC]ATTCCCTAGGCAGGT | 90293 |
rs780323937 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040746 | TAGCTCAAAGAAGAC[A/C]ACCTCAAGGCATTTA | 90293 |
rs780333384 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117910827 | TCTGGGCAACACAGC[C/T]TTCCTTAGCCACTCT | 90293 |
rs780341980 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118075418 | AACAAACTGAAGGAA[A/G]GCAAGTCCTGAAGTC | 90293 |
rs780351087 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118002242 | ATGGTTTGGTCAGGA[C/G]AGATGATTTAAAAAT | 90293 |
rs780360906 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118027088 | ATTTTGGGATGATCA[A/G]GACGTTTTGCTTGAG | 90293 |
rs780365199 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117952167 | TGTACTACAAGACTA[C/T]AGTAATCAAAACAGC | 90293 |
rs780375742 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117925230 | AAGCTACATTGATAC[C/T]GTCAGGTATTTAAAA | 90293 |
rs780377649 | snp | C/G | 2.28204e-05 | 0.00337782 | missense | KLHL13 | GRCh38.p7 | X:117899109 | CCCCCCAACCACATA[C/G]ATTTTATTTTCGAAG | 90293 |
rs780407214 | snp | C/T | 0 | 0 | intron-variant | KLHL13 | GRCh38.p7 | X:118036335 | ATCATGCTACCTGAC[C/T]TCAAACTATACTACA | 90293 |
rs780422061 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117957364 | CACTCTTGAAGTCAA[A/G]GCTTCCTGGCCTCAC | 90293 |
rs780427162 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118100446 | CTCCATTAAGAAAAA[C/T]ACTGATATTGTTATG | 90293 |
rs780428949 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118014845 | ATATTAAGACATTGT[C/T]TGTACCACAGAATGG | 90293 |
rs780450266 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118076460 | GTTTAGCATGCCTTA[A/G]ATAAAACTGCTTCCT | 90293 |
rs780450303 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051151 | CATATTCTATAAGTA[A/C]TGGAAAAAATACCAC | 90293 |
rs780480306 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118044636 | GAATATGCATTAGGG[-/A]AAGGACAGTCTCTTC | 90293 |
rs780491741 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117943525 | AGGCTTTGTTCGTTT[C/T]TTTTCATTCTTTTTT | 90293 |
rs780495503 | in-del | -/AT | 0.0214859 | 0.101397 | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118031445 | GATATATATATTTAG[-/AT]ATATATATAGATATA | 90293 |
rs780497112 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118036578 | CCTTCCTTATACCTT[A/T]TACAAAAATCAATTC | 90293 |
rs780508669 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118079636 | ACTGCTGAAAGAAAT[G/T]AAAGACAACACAAAT | 90293 |
rs780518629 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118007805 | TAGAAGAGAATCATA[A/G]TATGCCTATCTGTGG | 90293 |
rs780527617 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117995562 | AGTGGCATTCAGTGC[A/G]TTCAGAATGTTGCGC | 90293 |
rs780532658 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118020619 | ACTAGAAATACCATT[C/T]GACCCAGCCATCCCA | 90293 |
rs780546764 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117944314 | TCACATATCTATTGA[C/T]GACCCACAGGACAAT | 90293 |
rs780549406 | in-del | -/CA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118049025 | TTCAAATAAAGATTC[-/CA]GTTTATGACCTAGCG | 90293 |
rs780554218 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092752 | ACATGAATCCATAAT[A/G]TGATAAAATGTCACA | 90293 |
rs780557042 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117938556 | ATTCTGACATGCACT[-/A]AAATTTGAGAACCAT | 90293 |
rs780557143 | in-del | -/ATCT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118056941 | CCTCCGAGCACTTAA[-/ATCT]ATCTATCTCAGCTAC | 90293 |
rs780560294 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936858 | TTATTTCCATAAATT[C/G]TGACACTTAATCCTC | 90293 |
rs780562527 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118112545 | CGTACTCTATGCCAG[A/G]AATAATGCTAAGCAC | 90293 |
rs780564765 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118104084 | AAAAAATGCCAGGCA[G/T]GGTGATGTGCGCCTG | 90293 |
rs780567685 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118024086 | GTGTTATAAACTAGG[G/T]TCCATAAGACTAGGT | 90293 |
rs780573762 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117968943 | CAGGTACTGAATTTT[A/G]TTGAAGACATTACAG | 90293 |
rs780578231 | snp | A/C | | | utr-variant-3-prime | KLHL13 | GRCh38.p7 | X:117898752 | ATTCTAGGCCAAACA[A/C]AGAGCACAAATAACA | 90293 |
rs780579090 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117957987 | CATGACTAAAGTATT[C/T]TGGTCACTAGTAGAT | 90293 |
rs780584569 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117970270 | TGATAAAACATTACA[A/G]ACCAATACTGATGCT | 90293 |
rs780585015 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118031857 | ACTAGGGAGTGCCAG[G/T]CAGTGGGTGCAGGCC | 90293 |
rs780596419 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118072407 | GGCATTACCATTCAG[G/T]ACATAGGCATGGGCA | 90293 |
rs780613354 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | KLHL13 | GRCh38.p7 | X:117925890 | AGAAGGGGTTTCATC[A/G]TGTTACCCAGGCTGG | 90293 |
rs780614560 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118094301 | ATCAGCGATGGAAGA[C/T]GAAATGAATGAAATG | 90293 |
rs780623945 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:117999446 | ACTATCACAAGGACA[G/T]AAAACCAAATACCGC | 90293 |
rs780626368 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117961644 | AAGAGTGAGCCAGAA[G/T]GCAATGTGAAAAGGA | 90293 |
rs780635354 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118038125 | AACAGAAAATTGAAA[A/G]GATTACATCTAGATT | 90293 |
rs780644795 | in-del | -/AT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118047425 | TAATTCATAACACAC[-/AT]GACAGGCAACAAAGG | 90293 |
rs780653747 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118018351 | CACTTTTCATCATGC[-/T]TTTGCACGTGACAAT | 90293 |
rs780654062 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117948382 | TCTGCTCTCCACAGG[C/T]CCATCAATTTGAAAA | 90293 |
rs780664717 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117916737 | TAGGATAGAACAGAA[A/T]TGTATTAGAAGGGAA | 90293 |
rs780671344 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118032070 | AGGAGATTATATCCA[C/G]CACCTGGCTCAGAGG | 90293 |
rs780677711 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:117977338 | CAGTATAAGAGAAAA[C/T]GTAAATATATTGCCA | 90293 |
rs780692775 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117962082 | TGGGTGTGGTGATGC[A/G]TGCCTGTAGTCCCAG | 90293 |
rs780748989 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118000352 | AGATAAACTTAATTT[C/T]AATCTACTTTGATTA | 90293 |
rs780780854 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117940261 | GGTTGTAGATGTGTG[A/G]CATTACTTCTGAGGC | 90293 |
rs780783643 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118055100 | AGGGATTCAAGGGAG[C/T]ACAGCATGCAGGTCT | 90293 |
rs780797667 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118064442 | GTTAAAAAACATTTC[C/T]CTCCAAACTGAAGAA | 90293 |
rs780801810 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117992020 | AGCTGCCAGGATGAG[C/G]TGGCTATCAGTTATT | 90293 |
rs780802454 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117978217 | TATCAAGAAATATAA[A/T]TTAGTCAAAATCATC | 90293 |
rs780815693 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118097350 | TCAAAGAGAATAAAA[C/T]ACCTAGGAATCCAAC | 90293 |
rs780828306 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118097873 | GGAAAACTGGCTAGC[C/T]ATATGTAGAAAGCTG | 90293 |
rs780833634 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118033572 | ACCAGGCCTGCCCTA[A/C]AACAGATCCTGAAGG | 90293 |
rs780836102 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118025120 | TGTTTTCACCCAACA[C/T]GGCCACATATTATCC | 90293 |
rs780843287 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118107901 | TACAAAAAATACATA[A/G]AATTAGCCAGGCGTG | 90293 |
rs780849616 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118049782 | CTAGGGGGTCCAGAG[A/G]GGTATGTTCACAGCT | 90293 |
rs780857152 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117960150 | TGCGGGGCACAGGTT[C/G]GGGGCAGGGGGATAG | 90293 |
rs780864062 | in-del | -/AAA | 0.000405104 | 0.0142263 | intron-variant | KLHL13 | GRCh38.p7 | X:117983436 | AACCAATTCGCACTG[-/AAA]AAAAAAAAAAGGTGA | 90293 |
rs780872165 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118085488 | TTTGGTTACATGGAT[A/G]AAGTGTATAGTGGTG | 90293 |
rs780877159 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118004224 | GAACTCATGGTTTCA[A/C]TGGATAAAGATATAA | 90293 |
rs780887204 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118072997 | TACTCAGGAGGCTGA[G/T]GTGGGAGAATTGCTT | 90293 |
rs780926212 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118018759 | TATTATAAATTGATT[C/G]TTTGCCATTATATCT | 90293 |
rs780927657 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant, utr-variant-5-prime | KLHL13 | GRCh38.p7 | X:118029672 | CGCAATTTAGTTTAT[A/T]CATAAAGTTATGTTG | 90293 |
rs780930125 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117983382 | TACTGTAACTATACT[G/T]GATAACTGTCTTCTA | 90293 |
rs780933494 | snp | A/C | 0.00105904 | 0.0229869 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118117726 | ATCAGCCTAGCCCCC[A/C]AAAAAAACCCCAGTC | 90293 |
rs780936437 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118033313 | ACCAAAGTTGAAATG[A/C]AGGAAAAAATGTTAA | 90293 |
rs780943285 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118041124 | ACAAAATCTTCAGAA[-/G]GTACAAAACCTACTG | 90293 |
rs780966659 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118045703 | AATCTCAGCTACTCA[A/G]GAAGCTGACAAGAGA | 90293 |
rs780969153 | snp | C/G | 0.00105904 | 0.0229869 | utr-variant-3-prime, downstream-variant-500B | KLHL13 | GRCh38.p7 | X:117897970 | CAAGTTACCTCAACA[C/G]CAAAGGAGAAGGAGT | 90293 |
rs780970413 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118015315 | TATCTTATGTGATTA[C/T]TTACCCTGCATATAT | 90293 |
rs780979195 | snp | A/G | 2.30998e-05 | 0.00339843 | intron-variant | KLHL13 | GRCh38.p7 | X:117920416 | TCAAGGTAAAATGAG[A/G]TTACAAATCTTCGTG | 90293 |
rs780984229 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117915143 | TAACTTGCATTAAAT[C/T]GCCCTCAAAAGTGAA | 90293 |
rs780989617 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117925830 | ATCCTTCCTCCTTCA[A/G]AGACTAGCTTAAATT | 90293 |
rs780992205 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118054388 | AACTCTTGAAATCTA[A/G]ATGCAAGCAGCATTT | 90293 |
rs781015349 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997063 | AAAGACAAATGCTTT[C/T]GGGAAGACTCATACT | 90293 |
rs781025169 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118011829 | ATAAACATTTGTATT[A/T]ATGAGATCCAAAATA | 90293 |
rs781027975 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:117974611 | AATACAGCATGAAAT[C/T]AACTAACATAATCAC | 90293 |
rs781028415 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118116413 | CCTCTGCCCCTGGTA[C/G]AGATCGCAACTCCTC | 90293 |
rs781029690 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117924483 | AAGTCCTTTTACTGT[A/G]AAATCATTTTCTTTC | 90293 |
rs781030573 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118068382 | GAGAACACCAGGGTG[C/T]GTCAAAGGAGTAACA | 90293 |
rs781041336 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117916220 | ACAGTATTTAACATG[C/T]TGTAGTTATACAATG | 90293 |
rs781046445 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118100933 | TTCGGCAATTTTTTC[A/T]CAATCACCTCTTTCA | 90293 |
rs781050546 | snp | C/T | 2.28157e-05 | 0.00337747 | missense | KLHL13 | GRCh38.p7 | X:117899168 | TTAACATGGCAGCAA[C/T]TGGGGTCCACTGGTC | 90293 |
rs781062386 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938072 | CAAAGTTCATCCATA[C/T]GATAGCATGTATTAG | 90293 |
rs781082361 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118083793 | TGATTTGATCATTAC[A/T]TAATGTATATATGTA | 90293 |
rs781108838 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:117922501 | AGCTACCACTGGTAA[A/C]TTTAAAGCCATGTAG | 90293 |
rs781111081 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117932992 | ATTTTCCATATATCT[A/G]TTGGCCATTTGTATG | 90293 |
rs781113118 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118119340 | TGCTAAAAACACACA[C/T]ATTAATTATCTGTTT | 90293 |
rs781115933 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118011477 | GCTAAGACTAGAAGC[-/A]AAAAAAAAAAAACAG | 90293 |
rs781124996 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118095075 | TGGGCTAAATGCTCC[A/G]ATTAAAAGACACAGA | 90293 |
rs781142984 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117912985 | TTAATTTCAAAATGA[C/G]ACACAGACAAGAAAA | 90293 |
rs781147665 | in-del | -/AC | | | intron-variant | KLHL13 | GRCh38.p7 | X:118051650 | CTCACGCGCACATAC[-/AC]ACACACACACACACC | 90293 |
rs781158866 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117944138 | CAGACCCTGTTTGCC[C/T]GGGTATCACCAGTGG | 90293 |
rs781160081 | in-del | -/TCTCTCTCTCTCTCCT | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903622 | TACATTATTATTCTC[-/TCTCTCTCTCTCTCCT]TCTCTCTCTCTCGCC | 90293 |
rs781176683 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117946447 | ATACATTTGATAGTT[C/T]AAAAATCTCAGGTTA | 90293 |
rs781187584 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985945 | ATCCCATTCCATCTA[C/G]ATCGCTTTTTAAAAA | 90293 |
rs781197650 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118012935 | CTTATTTATTCAATC[A/G]TTTATTTCTATTAGT | 90293 |
rs781199509 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118004341 | TGGAACAGCAATACT[-/G]GAATAGCAATGAGCA | 90293 |
rs781211718 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118087263 | TTAACCACCTCTAGT[A/C]ATGTGAACTCCCTAT | 90293 |
rs781229776 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117938677 | TTAACTCATGACTAC[C/T]ATGGGCATTACATTA | 90293 |
rs781244749 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117989582 | AGTTACATAAATGAT[-/C]AACCTATACCTGTAC | 90293 |
rs781253689 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118046720 | AAAGCAGAAAAAGAA[C/T]ATATTCCCCATGAGA | 90293 |
rs781263923 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118070192 | AATTGCCTAAGGATG[C/G]ATTTCTCAGAATGTA | 90293 |
rs781268023 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117997806 | AATTCTATGTATTGA[G/T]GTATCTATTTTACTA | 90293 |
rs781273648 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117929498 | TGAAGAGTTTATAAC[G/T]CCAATGCAAGGTTGC | 90293 |
rs781275727 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118009242 | TTTGCTGTGCAGAAG[C/T]TCTTTAGTTGAATTA | 90293 |
rs781290872 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118005084 | AGCTTTCTGCTGTCA[A/G]TAACACTTTTGGGAT | 90293 |
rs781294262 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089057 | AGGGCAGAATATTAG[A/G]ACAGAAAATTTTTAG | 90293 |
rs781294567 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117955756 | TTTTCTGCATATCTG[C/T]CTCACCATTAAGGGT | 90293 |
rs781309087 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117994298 | TTGTTCTGTCACCCA[A/G]GCTGGAGTGCAGTAG | 90293 |
rs781316187 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118113724 | TCTGTATCATATTCC[C/T]CTACTTATTTTCATT | 90293 |
rs781325856 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117966154 | TGTATATCTAGAAAA[A/C]CCCATTGTCTCAGCC | 90293 |
rs781326914 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000407 | ACATCCAAAGATTAT[-/A]ACCAACAGCAATGTA | 90293 |
rs781352340 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118077834 | GGGGCTTGCAGCTTC[A/C]TGGGAACATTTATTC | 90293 |
rs781353767 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118001865 | GTGAGAGCAAGACCC[C/T]GTCAAAAAAAAAAAA | 90293 |
rs781365549 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117979835 | ATTCCAATAAAAAAA[-/T]CTCTATCACCTGAAA | 90293 |
rs781386110 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118089742 | TGCCATCAAAAAAAT[C/G]ATTTGCCATACCAAG | 90293 |
rs781391732 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117988932 | CTCTTAAATCAATTG[A/C/T]TATTTAATAGTTACA | 90293 |
rs781394415 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118005761 | TCCTTTAATTTTAGG[C/G]CAATGACCGGCAGAA | 90293 |
rs781396894 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117919807 | CAATAAAATCAAAGG[A/G]AAGTCTTATCTTATA | 90293 |
rs781398074 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118027482 | AAAGCAACTTGATTT[C/G]GGTGGAGCTTATATT | 90293 |
rs781414133 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117950940 | TTTCAGGGCTAAATC[A/T]GTCAAGGTATTTCCT | 90293 |
rs781417585 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118080278 | TTTGACAAACGAGAC[C/T]TAATTAAACTAAAGA | 90293 |
rs781431348 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118073235 | TAAGGAGGTTTAATG[C/G]ACTTACAGTTCCACA | 90293 |
rs781463678 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118051824 | GTAGTTCATTGGGAG[A/G]ACTGAACACATAAAA | 90293 |
rs781472723 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118059570 | TTAATGAAGAAAGTG[A/C]ATTTCAGAGATACAA | 90293 |
rs781492274 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903857 | ACTCTGACTTAAACT[C/T]TGAAATTTTTGGATT | 90293 |
rs781504574 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089950 | GCCAGGAATGGTGGC[A/G]TGTGCCTATAGTCCC | 90293 |
rs781505622 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117959977 | CAATTGCCCACATAC[A/G]CTCAACTGAGCTTGC | 90293 |
rs781523752 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118032406 | TCTGAGAACGGGCAG[A/T]CTGCCTCTTCAAGTG | 90293 |
rs781525599 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118075298 | GGTTTATGTGTAACT[C/T]AAAAAAAGATTTTTT | 90293 |
rs781531311 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118112449 | AGATCTAGTTCAATG[A/G]GGAATAGTGTAATAG | 90293 |
rs781534427 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117976378 | CACTATTCCTCACAT[A/C]TTATTTAGAAATAAA | 90293 |
rs781543412 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117971676 | CTGAGAGCATAACCA[C/T]ACTTCCTCAGCATCT | 90293 |
rs781559658 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118092633 | CATGGTAAGCAAAAT[A/G]TGTGTCAATACAACA | 90293 |
rs781561342 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118081617 | TTTCAAGTCTTCTAG[C/T]TATTTTGAAATATTC | 90293 |
rs781568174 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118040545 | AAAAAAGAATAAAGT[A/G]TACTTACAATATCTA | 90293 |
rs781585287 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | KLHL13 | GRCh38.p7 | X:118106228 | ATTAGTACAAAAGCA[C/T]TGGATTAGAAACTAA | 90293 |
rs781616073 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118026177 | CCTCAACCTTTCCTA[C/T]GTTTTCTGTTCATTT | 90293 |
rs781620156 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | KLHL13 | GRCh38.p7 | X:118052550 | AAAGTAGTAGAGGCC[A/G]GGCACAGTGGCTCAC | 90293 |
rs781625334 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118043632 | ATAGAAGGAAGGACA[A/G]AAACCTTATGATCAT | 90293 |
rs781631269 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117934487 | CCCTCTCTCCTACTA[A/T]CTTTGCCAAGATAAT | 90293 |
rs781640157 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118074714 | AGTAAAGTCATTTTT[G/T]ATTCAATGCCACCCA | 90293 |
rs781659995 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118099204 | TTTTCAAGTACAAAG[A/G]TATTATGGAAATAGG | 90293 |
rs781663571 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037322 | CGGCACTATTCACAA[C/T]AGCAAAGACTTGGAA | 90293 |
rs781667217 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118107321 | ACATTCACCATAAAC[G/T]TTCTTGTCTGCCAGA | 90293 |
rs781685714 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | KLHL13 | GRCh38.p7 | X:118020175 | TTATTTCCTTGAGCA[C/G]TGGTTTGTAGTTCTC | 90293 |
rs781686475 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | KLHL13 | GRCh38.p7 | X:118111388 | GTTTTGCCACCACAT[G/T]AGTTTTGGCATCTAA | 90293 |
rs781692505 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | KLHL13 | GRCh38.p7 | X:118036275 | AACCAAAAAAGAGCC[C/T]GCATCACCAAGGCAA | 90293 |
rs781696499 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | KLHL13 | GRCh38.p7 | X:118035544 | ACAAAATTCAACAAC[C/G]CTTCATGCTAAAAAC | 90293 |
rs781698332 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118039835 | CAGTCCCAGTGGTGG[C/T]TGCCACAGAGGTGCT | 90293 |
rs781698547 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117902165 | CATTAGACTAGATAG[C/T]GTAAGAATCTAACAA | 90293 |
rs781698640 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117921157 | TAACGACAAATAGAC[A/C]GTTGTTCTATTGATA | 90293 |
rs781698708 | in-del | -/GG | | | intron-variant | KLHL13 | GRCh38.p7 | X:117903173 | AGAGAGAGAGAGAGA[-/GG]AGAGCGAGAGAGAGA | 90293 |
rs781710983 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117936017 | TATCTCAATAAAGCT[A/G]TTATTTTAAAAACTG | 90293 |
rs781731631 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:117994009 | CCAAAGTGCTGGGAT[G/T]ACAGGCGTGAGCCAC | 90293 |
rs781732038 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968700 | CTAGAAAAGAAAGAT[A/T]TCTCTAATCACAAAT | 90293 |
rs781750706 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118060970 | TTCTTAAAAGGACAC[A/C]AGTTACATTGAATTA | 90293 |
rs781758245 | in-del | -/A | 0.00106213 | 0.0230204 | intron-variant | KLHL13 | GRCh38.p7 | X:118067272 | TACAGTATAAAAGAT[-/A]AAAAAATGGTACACC | 90293 |
rs781759619 | snp | A/T | 0.00581083 | 0.0535878 | upstream-variant-2KB, intron-variant | KLHL13 | GRCh38.p7 | X:117985448 | AGGCTTTATATATTT[A/T]AAAAAAAAAAAAAAA | 90293 |
rs781779766 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | KLHL13 | GRCh38.p7 | X:118057470 | AAGCATGAGCAACAA[C/T]AGATAATTTGGACTT | 90293 |
rs796130486 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037307 | CACGTATGTTTATTG[C/T]GGCACTATTCACAAT | 90293 |
rs796183015 | in-del | -/AA | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089613 | GAGAGAGAGAGAGAG[-/AA]AGAAAGAGAAAGAAA | 90293 |
rs796185329 | in-del | -/TT | | | intron-variant | KLHL13 | GRCh38.p7 | X:118000562 | GAAATTTCAAAAACA[-/TT]TTGGGGTCCTACATA | 90293 |
rs796208212 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094178 | AACTAGAATAACCAA[A/T]GCAGAGAAGTCCTTA | 90293 |
rs796212998 | in-del | AA/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118089592 | AAAGAAAAGAAAAGA[AA/G]AGAGAGAGAGAGAGA | 90293 |
rs796241429 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:117913848 | CTCCATCAAAAAAAA[A/G]AAAAAAAAAAAAAAG | 90293 |
rs796301788 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118045388 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAAGAAAT | 90293 |
rs796314321 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094188 | ACCAATGCAGAGAAG[C/T]CCTTAAAGGACCTGA | 90293 |
rs796443232 | snp | G/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037595 | TCTGGGGACTGTTGT[G/T]GGGTGGGGGAAGGGG | 90293 |
rs796464370 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118001149 | ACTGCAGACCTGTGA[A/C]AATATCCATAACAAA | 90293 |
rs796479041 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094165 | TAGATGAATGGCTAA[C/G]TAGAATAACCAATGC | 90293 |
rs796515217 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037629 | GGGATAGCATTGGGA[C/G]ATACACCTAATGCTA | 90293 |
rs796518972 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:117971405 | CTCCATTAACTTCTC[A/C]CCTCCATTAACTTGT | 90293 |
rs796567213 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:118090100 | AAAAAAAAAAAAAAA[-/A]CTGGATCCCTTCCTT | 90293 |
rs796584241 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118094174 | GGCTAACTAGAATAA[A/C]CAATGCAGAGAAGTC | 90293 |
rs796619428 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037642 | GAGATACACCTAATG[C/G]TAGATGACGAGTTAG | 90293 |
rs796666590 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037602 | ACTGTTGTGGGGTGG[A/G]GGAAGGGGGGAGGGA | 90293 |
rs796712925 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037317 | TATTGCGGCACTATT[C/T]ACAATAGCAAAGACT | 90293 |
rs796740268 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL13 | GRCh38.p7 | X:118030009 | AAAAAGAAAAAAGAA[A/G]TTATGTGAAGATCTA | 90293 |
rs796781382 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118036688 | ATAGGCATGGGCAAG[A/G]ACTTCATGTCTAAAA | 90293 |
rs796794144 | in-del | -/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117968174 | TAGAATTTTTTTTTT[-/T]CTATATAGCTCTATA | 90293 |
rs796798800 | snp | C/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:117911859 | TTTGCTTTACAAAAA[C/T]GTTTAATTGCTTATT | 90293 |
rs796814977 | snp | A/C | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037344 | GACTTGGAACCAACC[A/C]AAATGTCCAACAATG | 90293 |
rs796819833 | in-del | -/A | | | intron-variant | KLHL13 | GRCh38.p7 | X:117917425 | ATGCAAAAAAAAAAA[-/A]TGAACATGATATTTA | 90293 |
rs796855266 | snp | A/T | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037644 | GATACACCTAATGCT[A/T]GATGACGAGTTAGTG | 90293 |
rs796888894 | snp | C/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037604 | TGTTGTGGGGTGGGG[C/G]AAGGGGGGAGGGATA | 90293 |
rs797005120 | snp | A/G | | | intron-variant | KLHL13 | GRCh38.p7 | X:118037265 | ACCCAAAGGACTATA[A/G]ATCATGCTGCTATAA | 90293 |