SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs960707 | snp | A/T | 0.431769 | 0.17164 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919095 | TCTCCACACAAAAAA[A/T]TTTTGTTTTAATTAG | 59349 |
rs1042990 | snp | C/T | 0.495016 | 0.0496707 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892438 | GTCTGTTTCTCACTA[C/T]GTGCACCGGGTGATT | 59349 |
rs1418443 | snp | A/G | 0.354235 | 0.227234 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923847 | TTAGTTAGTTCTATC[A/G]TCTTAGTGTAGATAT | 59349 |
rs1539357 | snp | A/T | 0.495056 | 0.049474 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909326 | TTTGATCCATCTAGT[A/T]TGTTATCTATTTTTC | 59349 |
rs1977837 | snp | A/G | 0.431916 | 0.171483 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928268 | TTTTTTTTTGAGACG[A/G]AGTCTTGCTCTGTCG | 59349 |
rs1977838 | snp | C/T | 0.412416 | 0.190055 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928138 | ACTGGCGCCCGCCAC[C/T]ACGCCCAGCCAATTT | 59349 |
rs2275734 | snp | C/T | 0.496221 | 0.0433033 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918167 | GACGAAATTCAGGTA[C/T]GGATTTGTCTTGATG | 59349 |
rs2275739 | snp | C/T | 0.00500821 | 0.0497898 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893217 | ATTTAGAAACGAATC[C/T]AGACTCAATATGTAG | 59349 |
rs2363765 | snp | A/G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892431 | TGCCTGTAATCACCC[A/G/T]GTGCACATAGTGAGA | 59349 |
rs2363766 | snp | A/C | | | synonymous-codon, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892554 | CTCGCGGAGAACACA[A/C]ACACCAGCATCACAG | 59349 |
rs2363772 | snp | A/C | 0.343477 | 0.231866 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930233 | CTTTAATGATATTGC[A/C]TAATTCCTGACTGTT | 59349 |
rs3041271 | in-del | -/CAAA | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923885 | CAAAAAACAAACAAA[-/CAAA]AAACTTGTGCTTAAA | 59349 |
rs3182429 | snp | A/G | 0.390694 | 0.206652 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919819 | TGTGTACACAGAAAC[A/G]GTACATGTGACAGTG | 59349 |
rs3737886 | snp | A/G | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925335 | ATGCCAGGCATAGGA[A/G]TGCCCTCAACTTGTG | 59349 |
rs3766570 | snp | A/G | 0.00302808 | 0.0387926 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909171 | TTGTACTCTTATAGT[A/G]TTACAGGTATCCCCA | 59349 |
rs3766571 | snp | C/T | 0.0460142 | 0.144533 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890963 | ACAGGTAAGAGGTAG[C/T]CACTTTACACTTTGG | 59349 |
rs3766572 | snp | A/G | 0.433818 | 0.169443 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890939 | ACTTTGGAGATTCTC[A/G]TCAGTAAAATATTTA | 59349 |
rs3820152 | snp | A/T | 0.494733 | 0.0510469 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909364 | GAAATACTGCTCAAC[A/T]TATCTGTTTATATCA | 59349 |
rs3841739 | in-del | -/G | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927287 | ACTCTGGAGCGGGGG[-/G]AGGGCGGTGCTCCAG | 59349 |
rs4081384 | snp | A/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892469 | TAGTGGGAGAATCAA[A/G]AATCCTTTCCAGAAT | 59349 |
rs4388755 | snp | G/T | 0.103438 | 0.202533 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930413 | TTTTTTCTTCTTTTA[G/T]TTCCTCTTTTTTGTT | 59349 |
rs4950869 | snp | C/G | 0.118933 | 0.212888 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892437 | TAATCACCCGGTGCA[C/G]ATAGTGAGAAACAGA | 59349 |
rs4950887 | snp | C/T | 0.35445 | 0.227135 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901202 | TTTTCCCAATAAACA[C/T]TCTGGTAACTATATG | 59349 |
rs4950888 | snp | C/T | 0.495135 | 0.0490805 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903497 | caaggtcttgctctg[C/T]tgcccaggctagagt | 59349 |
rs4950889 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905658 | gtaatatctgcatta[C/T]ttctttgcacaacta | 59349 |
rs4950890 | snp | C/G | 0.293294 | 0.246223 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915104 | ATTTTCTCCACAATA[C/G]ATTTTCACAAAGAAT | 59349 |
rs6427976 | snp | G/T | 0.046775 | 0.145601 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891611 | ATTTGATCCAACAAA[G/T]AAAGGCTTTCACCCC | 59349 |
rs6427977 | snp | A/G | 0.349671 | 0.229272 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895221 | ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 59349 |
rs6427978 | snp | A/G | 0.351853 | 0.228311 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897287 | GTTGACCAGGCTAGA[A/G]TGCAATTCCATGATC | 59349 |
rs6427979 | snp | C/T | 0.492337 | 0.0614248 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900375 | atggtgagactccca[C/T]atctagaaaaaaata | 59349 |
rs6662398 | snp | G/T | 0.495174 | 0.0488838 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919328 | TGAAAATATCATACT[G/T]TAATATTTTGTGCAT | 59349 |
rs6662413 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919368 | TTTCATGTATCTTAA[C/T]GAAATACTACCACTT | 59349 |
rs6667300 | snp | C/T | 0.300169 | 0.244914 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924791 | TACTATTATCCCTAA[C/T]TTAAAGATGAGGAAA | 59349 |
rs6685274 | snp | C/G | 0.291493 | 0.246533 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910167 | AGAACCTATGAGGAA[C/G]GTACTATTATCATCC | 59349 |
rs6686801 | snp | C/T | 0.492386 | 0.0612297 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905602 | tatctgaaatgctta[C/T]gacaagaagcgctac | 59349 |
rs6686804 | snp | C/T | 0.34989 | 0.229177 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905612 | gcttacgacaagaag[C/T]gctacagatttcaga | 59349 |
rs6692075 | snp | C/T | 0.494568 | 0.0518327 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912174 | CACTGAAGAACATCA[C/T]CTAAGAGATAATTTG | 59349 |
rs7516884 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905014 | CTGGTTTAGCAGCCA[A/G]TATGCATAGAGATGG | 59349 |
rs7520522 | snp | C/T | 0.111224 | 0.207945 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920079 | agcactttgagaggc[C/T]aaggcaggcaaatca | 59349 |
rs7523420 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896576 | GCACGACCAATGAAA[G/T]GTGCTAGGAATTATA | 59349 |
rs7530468 | snp | C/G | 0.431621 | 0.171796 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902453 | AACACCAAAAACAAA[C/G]AAACAAAAAAACCTA | 59349 |
rs7531745 | snp | A/G | 0.354235 | 0.227234 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890640 | GTTTAATTAGCATGC[A/G]CAATCCATCTGCCAA | 59349 |
rs7532610 | snp | C/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908309 | cccaaccagtcattg[C/T]tggggcttggatttg | 59349 |
rs7536140 | snp | C/T | 0.433236 | 0.170072 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909680 | GCTCAGAAGACTGGC[C/T]TATATGAACTGTGTC | 59349 |
rs7542125 | snp | C/T | 0.431769 | 0.17164 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902110 | TGTAACATAATTTCC[C/T]TCCAGCCTTGTTTCT | 59349 |
rs7542327 | snp | C/T | 0.300421 | 0.244863 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902361 | CTTGAACTTGGGAAG[C/T]GGAGACTGCAGTGAG | 59349 |
rs7543722 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899832 | catctcaaaaaaaaa[A/T]aaaaaaaataataat | 59349 |
rs7543724 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899838 | aaaaaaaaaaaaaaa[A/T]aataataataataaa | 59349 |
rs7548635 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906380 | gaatcgcttgaaccc[A/G]ggagacagaggttgc | 59349 |
rs7548700 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906403 | gaggttgcagtgagc[A/C]aagattatgccactg | 59349 |
rs8179338 | snp | A/G | 0.300169 | 0.244914 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913175 | ATCTGGGGAACTTAG[A/G]TCTAAGCATACATAT | 59349 |
rs9651059 | snp | C/G | 0.433236 | 0.170072 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916806 | CAACACAGCGAGACC[C/G]CATCTCAACAAAAAT | 59349 |
rs9700677 | snp | C/T | 0.428635 | 0.174898 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899776 | TGCAGTGAGCCGAGA[C/T]TGCACCACTGCACTC | 59349 |
rs9919219 | snp | C/T | 0.300169 | 0.244914 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908269 | TTAGTGGTAGACATA[C/T]AGGCTCAGATAAATT | 59349 |
rs9943282 | snp | C/T | 0.492337 | 0.0614248 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926012 | AAGAAGGCTGAGGCC[C/T]GAGAATCACTTGAAC | 59349 |
rs10577552 | in-del | -/TCTC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911457 | ATATATATATATGTA[-/TCTC]TCTCTCTCTCTCTCT | 59349 |
rs10612618 | in-del | -/AA | 0.0228947 | 0.104514 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899823 | GTAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 59349 |
rs10641768 | in-del | -/CCT | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917456 | GACACAAGCAGTTCT[-/CCT]GCCTCAGCCTCCCAA | 59349 |
rs10732291 | snp | A/G | 0.495174 | 0.0488838 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922040 | CATTTAATAATTATG[A/G]TACTGAAATATGTAA | 59349 |
rs10732292 | snp | C/T | 0.492386 | 0.0612297 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922238 | ATTCTCACAGCAACC[C/T]GGTAAGGTAGTTAGG | 59349 |
rs10753926 | snp | C/T | 0.495174 | 0.0488838 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906957 | GTGAGACACCGTGCC[C/T]GGCCTGTTACATATA | 59349 |
rs10753927 | snp | C/T | 0.304438 | 0.244001 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912481 | TGGTGGTGGATATGG[C/T]GGCAGTGAGGATGGC | 59349 |
rs10753928 | snp | A/C | 0.495174 | 0.0488838 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921917 | AAAATCAATCCCTAA[A/C]ACTAAAAAAGTCACT | 59349 |
rs10800877 | snp | C/T | 0.41325 | 0.18934 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914935 | GAAAGAAATCTGTAA[C/T]TGATTGTGGTCAACA | 59349 |
rs10800878 | snp | C/G | 0.354235 | 0.227234 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920277 | CAAGATTGTGCCACT[C/G]CACTCCAGCCTGGGC | 59349 |
rs10800879 | snp | C/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921165 | ACAGGAGTACACCAC[C/T]ACAACCAGCTAATTT | 59349 |
rs10800880 | snp | C/T | 0.413748 | 0.188909 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923789 | CATAAAAGGTAGTTA[C/T]TACCATCACAGAATA | 59349 |
rs10800881 | snp | A/T | 0.356169 | 0.226336 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925612 | TTTAGAGCATACATA[A/T]AAAGAGGATCCTGCT | 59349 |
rs10800882 | snp | A/G | 0.496314 | 0.0427728 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928303 | AGAAAAAAGAAAAAA[A/G]AGAAAAAACAAAAAA | 59349 |
rs10920519 | snp | A/C | 0.413748 | 0.188909 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897203 | AGAAAGCAAACTTCA[A/C]CATGACACTGCACCA | 59349 |
rs10920521 | snp | C/T | 0.356383 | 0.226236 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916419 | AGCATTTTAGGAGGC[C/T]GAAGTGGCTGATGTC | 59349 |
rs10920522 | snp | A/G | 0.333491 | 0.235646 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923092 | TGGACTCTCTCCTTT[A/G]AACAATTACTCTCAA | 59349 |
rs10920523 | snp | G/T | 0.495095 | 0.0492773 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923146 | ATTTCCTTGCCTGAT[G/T]TCAGTTTTTAAAGAA | 59349 |
rs10920524 | snp | G/T | 0.495095 | 0.0492773 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923147 | TTTCCTTGCCTGATG[G/T]CAGTTTTTAAAGAAA | 59349 |
rs10920525 | snp | C/T | 0.119281 | 0.213102 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924586 | gcaacatagtgagac[C/T]ctgtctctacaaata | 59349 |
rs10920526 | snp | C/T | | | intron-variant, upstream-variant-2KB, splice-acceptor-variant | KLHL12 | GRCh38.p7 | 1:202927516 | GGCAAAACCCCGTTT[C/T]TACAAAAAAAAAAAA | 59349 |
rs10920527 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927518 | CAAAACCCCGTTTCT[A/C]CAAAAAAAAAAAAAA | 59349 |
rs11305071 | in-del | -/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897229 | TTTTTTTTTTTTTTT[-/T]GGAGACAGAGTTTCG | 59349 |
rs11366890 | in-del | -/T | 0.34989 | 0.229177 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900919 | GTGTGGTGGTGTGCA[-/T]TTTGTAGTCCCAGCT | 59349 |
rs11403422 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928282 | CAAAAAAAAAAAAAA[-/A]GAAAAAAGAAAAAAG | 59349 |
rs11404714 | in-del | -/T | 0.485187 | 0.0847778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903460 | TCTTGTTTTTTTTTT[-/T]CTTTTTTGAGACAAG | 59349 |
rs11584998 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923859 | AGATGATAGAACTAA[A/C]TAAAAAAAAAACAAA | 59349 |
rs11801140 | snp | G/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921808 | CTTAAAAAACTCTGG[G/T]GCATCTCCATTATTA | 59349 |
rs11806328 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892743 | actatgcaggaggct[A/G]aggtaagaggattgc | 59349 |
rs11809627 | snp | A/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901474 | ttttttttttttttt[A/T]aattttttaaagaga | 59349 |
rs11811101 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901476 | tttttttttttttta[A/T]ttttttaaagagagg | 59349 |
rs12034646 | snp | C/T | 0 | 0 | missense | KLHL12 | GRCh38.p7 | 1:202919902 | AAGGTTTCCCCTTCT[C/T]TGAGAGCTGAAAATT | 59349 |
rs12037706 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923074 | gcctagaatccaggt[A/C]tctggactctcTCCT | 59349 |
rs12043834 | snp | C/T | 0.118933 | 0.212888 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906526 | gagtttattgtttaa[C/T]gggtacagagtttca | 59349 |
rs12067508 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903624 | accacTAAttttttt[C/T]ttttctttttttttt | 59349 |
rs12067510 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903629 | TAAtttttttctttt[C/T]tttttttttttgaaa | 59349 |
rs12070941 | snp | C/T | 0.433236 | 0.170072 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916500 | AAATACAAAAATTAG[C/T]TGGTGTAGTGGTGGG | 59349 |
rs12074142 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913324 | TGCCCCTTCTACCAG[C/T]CCCTACAGAGTACAT | 59349 |
rs12089566 | snp | A/G | 0.433382 | 0.169915 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892214 | CATATGAGGCACAAC[A/G]TACATATAGTACACC | 59349 |
rs12091309 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916416 | ctcagcattttagga[A/G]gctgaagtggctgat | 59349 |
rs12092574 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916972 | agtgagaccatctca[C/G]aagaaaaaaaaaaaa | 59349 |
rs12094608 | snp | A/T | 0.11963 | 0.213316 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904377 | TGTATATGATTTTTT[A/T]ATTTATTCAAATATG | 59349 |
rs12117507 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927836 | aatacaaaaaaatta[C/G]ccgggcgttgtggca | 59349 |
rs12118311 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927892 | gaggctaatgcagga[A/G]aatcgctagaacctg | 59349 |
rs12118322 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927969 | tgggcgaccgactga[A/G]actctgtctcttaaa | 59349 |
rs12133632 | snp | A/C | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923565 | TTCATACTTCGGAGG[A/C]TAAGGCGGCACAAGA | 59349 |
rs12145794 | snp | A/C | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903019 | caaaTGAAATAGATC[A/C]Ccatggtggcatacg | 59349 |
rs12562006 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897522 | agtcactgtgcccgg[C/G]AACACTGCACCATTT | 59349 |
rs12567643 | snp | A/G | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909833 | aaccttgtcccttca[A/G]gcttaggggttgtta | 59349 |
rs12569087 | snp | A/G | 3.29848e-05 | 0.00406095 | missense | KLHL12 | GRCh38.p7 | 1:202919889 | TGGATGTCAACATAA[A/G]GTTTCCCCTTCTCTG | 59349 |
rs12723144 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912084 | ACCAAAGAGAGCTGT[C/T]TCAAGGGAAGATTCT | 59349 |
rs12723261 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912114 | TCAAAGACCAGGTGC[C/T]CACTTAACTGTGAAA | 59349 |
rs12723440 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912231 | GAAATCATGACTGAC[C/T]GAGGCAGTGGCAAGA | 59349 |
rs12728803 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905994 | ttttttttttttttg[C/G/T]atttttagtagatac | 59349 |
rs12738396 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920394 | ttttttttttttttt[G/T]gagacggaatcttgc | 59349 |
rs12739257 | snp | A/G | 0.0154232 | 0.0864508 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916974 | tgagaccatctcaga[A/G]gaaaaaaaaaaaaaa | 59349 |
rs12739674 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916975 | gagaccatctcagaa[A/G]aaaaaaaaaaaaaaT | 59349 |
rs12741166 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912145 | AAGATATTTGTTGGC[A/G]GCATTAAAGAAGACA | 59349 |
rs12741306 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912144 | AAAGATATTTGTTGG[C/T]AGCATTAAAGAAGAC | 59349 |
rs12741315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912159 | CAGCATTAAAGAAGA[C/T]ACTGAAGAACATCAC | 59349 |
rs12741322 | snp | C/T | 0.0111728 | 0.0739025 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912175 | ACTGAAGAACATCAC[C/T]TAAGAGATAATTTGA | 59349 |
rs12741542 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912090 | GAGAGCTGTTTCAAG[A/G]GAAGATTCTCAAAGA | 59349 |
rs12741701 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912232 | AAATCATGACTGACT[A/G]AGGCAGTGGCAAGAA | 59349 |
rs12747139 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906021 | atacggggtttcacc[A/G]tgttagcctggatgg | 59349 |
rs12752406 | snp | A/G | 0.351853 | 0.228311 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914113 | TTAAGCAAGGGCCAG[A/G]TACAGAGAGCATTAG | 59349 |
rs12756649 | snp | C/T | 0.495407 | 0.0477027 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920566 | TACTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 59349 |
rs16850747 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911639 | TGAAATAATTTTAAG[A/G/T]CATAATTGTTATCTA | 59349 |
rs16850750 | snp | A/C | 0.41507 | 0.187755 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911677 | CCAGGCTCACCCCTC[A/C]AACTGTTCACCCAAG | 59349 |
rs17552601 | in-del | -/G | 0.431029 | 0.17242 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927286 | CGCAGACTCTGGAGC[-/G]GGGGGGAGGGCGGTG | 59349 |
rs17552608 | snp | A/T | 0.13446 | 0.221699 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927270 | GGGCGGTGCTCCAGC[A/T]GCATTGCGTCATCAC | 59349 |
rs28436163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911443 | ATATACACACACACA[C/T]ATATATATATGTATC | 59349 |
rs28504294 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911445 | ATACACACACACATA[C/T]ATATATATGTATCTC | 59349 |
rs28505411 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922794 | CCCAGCTGAAGATCC[A/C]AGACTTAACCAGTCA | 59349 |
rs28653277 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922795 | CCAGCTGAAGATCCA[A/C]GACTTAACCAGTCAC | 59349 |
rs34058797 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925268 | CAACTGAACATATTT[-/T]AATTAGCTTTACAAA | 59349 |
rs34187527 | in-del | -/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915845 | TAGAATGGAAGCTCC[-/C]AGTGGACAGGGATTT | 59349 |
rs34231569 | in-del | -/A/AA | 0 | 0 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892096 | GGAAAAAAAAAAAAA[-/A/AA]GACTTGGATTTTACC | 59349 |
rs34394629 | in-del | -/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917969 | TTCTTACCCACTGGG[-/G]ATCATATATCTAATT | 59349 |
rs34564688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915978 | AAGTATTAGCTATTA[C/T]ATGTAGTGAACGTCA | 59349 |
rs34656704 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910181 | CGTACTATTATCATC[-/T]CCTGTTTTACACATA | 59349 |
rs34664775 | in-del | -/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928567 | TCCACAATGGCCTTT[-/T]CGGGCCGAACAACGC | 59349 |
rs34751045 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927997 | AAAAAAAAAAAAAAA[-/A]GGCCAGGCGAGGTGG | 59349 |
rs34773990 | in-del | -/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926788 | AGATTCGGGGCAGGG[-/C]AATGGGTAGTAAACT | 59349 |
rs34815999 | in-del | -/A | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907613 | AAAAAAAAAAAAAAA[-/A]GGAAAAAAATTATAT | 59349 |
rs35167660 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918904 | TATTAAAAACTAAAA[-/A]GTGTGTCAATTATGT | 59349 |
rs35293504 | multinucleotide-polymorphism | GT/TG | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923146 | ATTTCCTTGCCTGAT[GT/TG]CAGTTTTTAAAGAAA | 59349 |
rs35325864 | in-del | -/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921745 | TATCTGAAAATACCT[-/C]TATGAAAATTTTACT | 59349 |
rs35914469 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903295 | TGGATAGTTTTTAAA[-/A]TCTCTGACACTCTGG | 59349 |
rs36014595 | in-del | -/T | | | intron-variant, upstream-variant-2KB, frameshift-variant | KLHL12 | GRCh38.p7 | 1:202927466 | GCGAGCGAATTACCT[-/T]GAGCTCCGGAGTTCC | 59349 |
rs36072537 | in-del | -/CTCT | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911468 | TCTCTCTCTCTCTCT[-/CTCT]AAGATAGATAGTACC | 59349 |
rs36105813 | in-del | -/A | 0.494609 | 0.0516363 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904370 | ATAATTTTGTATATG[-/A]TTTTTTTATTTATTC | 59349 |
rs36141808 | in-del | -/T | 0.482728 | 0.0913109 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911419 | TGGGTTAAAAAAAAA[-/T]ATATATATATATACA | 59349 |
rs41264019 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891552 | TACTGTCACTCCCAG[C/G]CCATCCCCAAATAAA | 59349 |
rs55724804 | snp | A/G | 0.00873562 | 0.0655095 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892507 | ACTGGACTGGTCACT[A/G]GCTCTGGATGGTGCT | 59349 |
rs55731233 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895444 | GTATTTCATGCTCCT[A/G]CCAGACAACAGGAGA | 59349 |
rs56210546 | snp | A/T | 0.0217236 | 0.101931 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929848 | ATATGTTCAATTTTT[A/T]AAAAAGTAAAAATAG | 59349 |
rs56658940 | in-del | -/T | 0.365646 | 0.221644 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901459 | CCAAACCCAGCTACC[-/T]TTTTTTTTTTTTTTT | 59349 |
rs56676311 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899823 | GTAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 59349 |
rs57537438 | in-del | -/TTTTTTTTTTTTT/TTTTTTTTTTTTTTT | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903640 | TTTCTTTTTTTTTTT[lengthTooLong]GAAACGGCGTCTTGC | 59349 |
rs57662282 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920505 | GCTCAGCCTCCCGAG[C/T]AGTTTGGACTACAGG | 59349 |
rs57973720 | in-del | -/CTCTCT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911474 | TCTCTCTCTCTCTCT[-/CTCTCT]AAGATAGATAGTACC | 59349 |
rs58045648 | snp | A/T | 0.499538 | 0.0151974 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911419 | TTGGGTTAAAAAAAA[A/T]ATATATATATATACA | 59349 |
rs58279012 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920496 | ATTCTCCTGGCTCAG[C/T]CTCCCGAGTAGTTTG | 59349 |
rs59164156 | in-del | -/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904015 | TATCTATCTATCTAT[-/C]TTATCTATCTATCTA | 59349 |
rs59171170 | snp | G/T | 0.433236 | 0.170072 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901512 | TCACTATGTTGCTCA[G/T]GCTGGTCTCTAACTC | 59349 |
rs59435824 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906479 | AAAAAAAAAAAAAAA[-/A]GTTCCTACCCTGGGA | 59349 |
rs59667776 | in-del | -/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904016 | ATCTATCTATCTATT[-/C]TATCTATCTATCTAT | 59349 |
rs60802038 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899433 | CTCACACATAAACCA[C/T]GGAGTTTTTCTAAGA | 59349 |
rs61345578 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900231 | TGCCCCACCCCCCAA[A/C]CCCCCAAAAATAAAT | 59349 |
rs61821054 | snp | A/G | 0.357024 | 0.225933 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906370 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGA | 59349 |
rs66478765 | in-del | -/G | 0.495016 | 0.0496707 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922282 | TATCTAAGAGATAAA[-/G]GGGGGGCCGGGCACA | 59349 |
rs66479468 | in-del | -/A | 0.338296 | 0.233889 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907598 | GCAAGACTCTGTCTT[-/A]AAAAAAAAAAAAAAA | 59349 |
rs66824268 | in-del | -/CTC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917455 | GGACACAAGCAGTTC[-/CTC]TGCCTCAGCCTCCCA | 59349 |
rs66898765 | snp | A/G | 0.43221 | 0.171171 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898641 | ATGTTAAATGACACT[A/G]CAAAGATGCAACAGC | 59349 |
rs67039834 | snp | A/G | 0.41325 | 0.18934 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914235 | ATCCTGGCTACTGTG[A/G]GTAGAACAGTTTAAA | 59349 |
rs67432749 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903160 | TTTTTTTTTTTTTTT[-/T]GAGACAAGGTCTCAC | 59349 |
rs67830135 | in-del | -/A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911420 | GGGTTAAAAAAAAAA[-/A/T]TATATATATATACAC | 59349 |
rs71142574 | in-del | -/A | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905992 | ATCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA | 59349 |
rs71635598 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903807 | TTTATACTTTTAGTA[A/G]AGACAGGGTTTCATC | 59349 |
rs72752781 | snp | C/T | 0.350764 | 0.228794 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918644 | AAGATGAATCACATC[C/T]AGAGACCTGGCACAA | 59349 |
rs72752784 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919422 | TCCATGTAGGCTATG[C/T]ATAGTATCACTTTTT | 59349 |
rs72752786 | snp | C/T | 0.35207 | 0.228214 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923010 | TACAGATCAACCCAG[C/T]GAAGTTAGATGGTTC | 59349 |
rs72752787 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926124 | AAAAAAAAAAAAAAA[A/G]AAACTTCAATTGAGG | 59349 |
rs73089386 | snp | A/G | 0.41325 | 0.18934 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900454 | ACTCCTGAGGCTGAC[A/G]TGGGAGGATCACTTA | 59349 |
rs73089390 | snp | A/G | 0.433382 | 0.169915 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906222 | CTTTAGGAGGCTGAG[A/G]TGGGCGGATCACCTG | 59349 |
rs73089392 | snp | C/G | 0.431769 | 0.17164 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906289 | GAAACCCCGTCTCTA[C/G]TAAAAAATACAAAAA | 59349 |
rs73089402 | snp | A/G | 0.119281 | 0.213102 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914364 | AGAAATACTTGGGAA[A/G]TTAAACTAACCCAGG | 59349 |
rs73091308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918126 | TTTGCAAGTTTTGTA[A/G]TTGCCCAATCTTGAA | 59349 |
rs74136922 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909394 | CCCATCTATCGCAGC[A/G]CTTACATTTAACTAT | 59349 |
rs74409416 | snp | A/G | | | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895635 | ACTGAACTAAGGCGG[A/G]AACGGCCATCATAGC | 59349 |
rs74624189 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927697 | AAAAAAAAAAAAAAA[A/T]GTCCAGGCGTGGTGG | 59349 |
rs74693273 | snp | G/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896156 | AATTACTATTGTTCA[G/T]TCAGCACTGAGAGAC | 59349 |
rs75050002 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893816 | GCACAGTGCTCTCTC[C/T]TTTTCTATATCCCAG | 59349 |
rs75118595 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915353 | ATTTAATAAGAGGGA[G/T]CAATAGCAACTGGGA | 59349 |
rs75132116 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915842 | CCACTAGAATGGAAG[A/C]TCCAGTGGACAGGGA | 59349 |
rs75225221 | snp | C/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901460 | CAAACCCAGCTACCT[C/T]TTTTTTTTTTTTTTA | 59349 |
rs75282530 | snp | C/T | 0.0248432 | 0.108648 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930414 | TTTTTCTTCTTTTAT[C/T]TCCTCTTTTTTGTTA | 59349 |
rs75368350 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920317 | AGACTCCATTTCAAA[A/C]AAATAAAAAAGAAAG | 59349 |
rs75389942 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923539 | TTAAAATTAGATTGT[A/T]GTATATAAAATTCAT | 59349 |
rs75465624 | snp | G/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915514 | TCAAGCTGTTTTTCA[G/T]TTAAGCTTCTAAATA | 59349 |
rs75561647 | snp | C/T | 0.102726 | 0.202016 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926350 | CAAAAGTCCACAAGT[C/T]ACAATTAATCTTTCA | 59349 |
rs75823601 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919273 | AAACAAAACAAAAAA[C/T]CTGGGAATTGTAAGG | 59349 |
rs75907557 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903471 | TCTTGTTTTTTTTTT[C/T]TTTTTTGAGACAAGG | 59349 |
rs75925857 | snp | A/G/T | 0.0232847 | 0.105357 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929173 | GCCAAGTGGGTAGCA[A/G/T]TCTAAATTTACAACG | 59349 |
rs76179796 | snp | A/C | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923871 | TAACTAAAAAAAAAA[A/C]AAAAAACAAACAAAA | 59349 |
rs76258902 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913928 | CAACACGGGGCTAGC[A/G]GGAGCAAACCAGACA | 59349 |
rs76259261 | snp | A/C | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905365 | TCATGCAAAAAGGAA[A/C]CATTTTTCTGTGTTG | 59349 |
rs76285843 | snp | A/T | 0.0818113 | 0.184966 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930157 | CTCAAATAAATAAAT[A/T]AATTAATTAAATTAA | 59349 |
rs76538156 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914459 | ATATGATTGGAAAAT[A/G]GTTTTAAGCAGATAC | 59349 |
rs76713614 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908566 | GTAACTGCCAAAACC[A/C]ATGTACTTTCTACCA | 59349 |
rs76919961 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899464 | GGGCACTTGTCTTAT[A/G]TACTTGCCAAATAAA | 59349 |
rs77064645 | snp | A/G | 0.0349115 | 0.127424 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890817 | AGGACTGGTGTGACT[A/G]AAACCCTGAAATTCA | 59349 |
rs77092008 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900148 | AAGAGGTACTTCCTG[C/T]GCTATGCAAATTTTA | 59349 |
rs77218625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922864 | TTTCAGGAAAAAAAA[A/G]AGAGAGAGAGAGAGA | 59349 |
rs77248588 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895891 | AGCTACCTACTGAAC[A/G]AAATGCCTGTTGTGG | 59349 |
rs77397895 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910409 | CTGACCATGCTGCAA[C/G]TTTTCTAATGTGAAC | 59349 |
rs77432739 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927360 | CCTAGCGCGGGGCTT[C/T]TGTACGCTGCTAGGA | 59349 |
rs77487821 | snp | A/G | 0.013097 | 0.0799021 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927307 | CGCTCCAGAGTCTGC[A/G]TCACGTGAGGAGGTG | 59349 |
rs77499001 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911460 | TATATATATGTATCT[A/C]TCTCTCTCTCTCTCT | 59349 |
rs77503044 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919082 | TAGAGAGAACTCATC[G/T]CCACACAAAAAAATT | 59349 |
rs77544559 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924435 | CTTATCCCTCTGGTA[G/T]TCACTTAAAAATTTT | 59349 |
rs77609694 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906694 | TGAGATGGAGTCTCA[C/T]TCTGTCGCCCAGGCT | 59349 |
rs77636922 | in-del | -/AC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924862 | CTGCCAAAACATCAC[-/AC]TGTAAAAATTCAAAA | 59349 |
rs77697211 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906695 | GAGATGGAGTCTCAC[G/T]CTGTCGCCCAGGCTG | 59349 |
rs77911381 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899650 | GTCTAACATGGCAAA[A/T]CCCCGTCTCTACTAA | 59349 |
rs77960042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919272 | AAAACAAAACAAAAA[A/G]CCTGGGAATTGTAAG | 59349 |
rs78283166 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927997 | AAAAAAAAAAAAAAA[A/G]GGCCAGGCGAGGTGG | 59349 |
rs78311273 | snp | A/G | 0.00581108 | 0.0535889 | missense, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202925173 | CCCATAAAGCAGTGC[A/G]GAGAAAGAACAAAAT | 59349 |
rs78427595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926623 | CGTTTCCGTGTCAAA[A/C]TGACAGTACCCCGGT | 59349 |
rs78442588 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897520 | TGAGTCACTGTGCCC[A/G]GCAACACTGCACCAT | 59349 |
rs78493288 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905175 | TATATAGATTTATAG[C/T]TTAATCCCTTAAGGT | 59349 |
rs78520698 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904363 | ATTTATCATAATTTT[A/G]TATATGATTTTTTTA | 59349 |
rs78559215 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921477 | ACCATGCCCGGCCCT[C/T]AGACTGCATTTAGTA | 59349 |
rs78736525 | snp | G/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921193 | TTTTTTTTTTTTTTT[G/T]TGACACAGTCTTGCT | 59349 |
rs78958889 | snp | C/T | 0.167158 | 0.235875 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922667 | AATTTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 59349 |
rs79043855 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924440 | CCCTCTGGTATTCAC[C/T]TAAAAATTTTTAAAC | 59349 |
rs79202931 | snp | A/T | 0.102726 | 0.202016 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919516 | CTCCATTTTTTTTTT[A/T]AAACAGAAAAGGTGC | 59349 |
rs79284271 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928848 | TTTTTTTTTTTTTTT[G/T]AGACGGACTCTTGCT | 59349 |
rs79425353 | snp | C/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897740 | TTTAAAATCTCTTTT[C/T]CTTTTTCTGAATTGA | 59349 |
rs79504140 | snp | A/G | 0.413416 | 0.189196 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906109 | CGGGCATGAGCCACC[A/G]CGCCCGGCCACCCAA | 59349 |
rs79732518 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897982 | TAGAGTTTTAAAGGA[A/G]AAGTCTTTTTCTCTA | 59349 |
rs79946437 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910107 | ACTTATGTACAAAGA[C/T]TTGGTTTTAAAAGTT | 59349 |
rs80147998 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928406 | GTTCCTCCCTACCGC[C/T]CACTAGGCAGGGCAG | 59349 |
rs111266690 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918847 | AGTATTTTAATGTTA[C/T]GGCTATGCACTAATG | 59349 |
rs111348715 | snp | A/G | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922434 | TAGCCAGGCGTCAAG[A/G]AAAAAAAAAAAAAGA | 59349 |
rs111401543 | snp | A/G | 8.29703e-05 | 0.00644036 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911227 | GTATAATTACACACC[A/G]TGGATCCTACTTTTC | 59349 |
rs111452276 | snp | C/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896768 | ATTAGGCTTTTCTAC[C/T]CTTAAGGCTGGATTA | 59349 |
rs111461718 | in-del | -/A | 0.49263 | 0.0602539 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916975 | GAAAAAAAAAAAAAA[-/A]TTAAAGAATTGGACC | 59349 |
rs111650099 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898658 | AAAGATGCAACAGCA[C/G]AGTCTAGAATGTGGG | 59349 |
rs111756741 | snp | A/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923473 | GTTCCTGTTTTCCCT[A/T]CTAGCCATGTGACTG | 59349 |
rs111844612 | snp | A/T | 0.207559 | 0.246371 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906100 | CTGGGATTACGGGCA[A/T]GAGCCACCGCGCCCG | 59349 |
rs112019147 | snp | A/C/G | 6.9035e-05 | 0.00587481 | missense, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202925206 | GTCCTTGGATTCTGC[A/C/G]ACTACAAGAGGGAAA | 59349 |
rs112465758 | snp | A/C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928289 | CAAAAAAAAAAAAAA[A/C/G]AAAAAAGAAAAAAAA | 59349 |
rs112531778 | snp | G/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896509 | ACTTCTGAGCTCAAC[G/T]GAACACTGGGTTCAA | 59349 |
rs112552780 | snp | G/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912504 | AGGATGGCGATAATG[G/T]ATTTGGTAATGATGG | 59349 |
rs112619286 | snp | G/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910599 | ACAGAGAACTTAAGT[G/T]GGAGAAACACTTTTA | 59349 |
rs112623717 | snp | C/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908273 | TGGTAGACATACAGG[C/T]TCAGATAAATTGATA | 59349 |
rs112653378 | in-del | -/CTC | 0.34989 | 0.229177 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917454 | TGGACACAAGCAGTT[-/CTC]CTGCCTCAGCCTCCC | 59349 |
rs112684672 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899835 | CTCAAAAAAAAAAAA[A/T]AAAAATAATAATAAT | 59349 |
rs112710040 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927977 | CGACTGAGACTCTGT[C/T]TCTTAAAAAAAAAAA | 59349 |
rs112884263 | in-del | -/A | 0.43309 | 0.17023 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899647 | CCTGTCTAACATGGC[-/A]AAACCCCGTCTCTAC | 59349 |
rs113109210 | snp | C/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895157 | AGCACCTTGGGAGGC[C/T]GAGGTGGGTCAATCA | 59349 |
rs113156256 | snp | C/G | 0.444444 | 0.157135 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924492 | ATGCCGTGGCTCACA[C/G]CTGTAATGCCAGGTG | 59349 |
rs113158028 | snp | A/C | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918133 | GTTTTGTAATTGCCC[A/C]ATCTTGAAGAAACCA | 59349 |
rs113242526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900033 | TCTTCCTGACTTGAA[C/T]AGACAAGGTAAGTGT | 59349 |
rs113466142 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929192 | AAATTTACAACGTGT[C/T]CCCATCTTCCATGTC | 59349 |
rs113569535 | snp | C/G | 0.444444 | 0.157135 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922828 | AGCTAGTAAGAGACA[C/G]ATATCATTCTTATTA | 59349 |
rs113674571 | snp | A/G | 0.5 | 0 | missense | KLHL12 | GRCh38.p7 | 1:202894735 | CATCAAAGCCTCCAG[A/G]GACATAGATCATATC | 59349 |
rs113751053 | snp | A/G | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923572 | TTCGGAGGCTAAGGC[A/G]GCACAAGAGTTACAA | 59349 |
rs113755389 | snp | C/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924864 | GCCAAAACATCACAC[C/T]GTAAAAATTCAAAAT | 59349 |
rs113851253 | snp | C/T | 0.5 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894166 | GCCTATTGTCCCCTC[C/T]CTCAGATCTGGTCTT | 59349 |
rs113974527 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892129 | GTTTACTTAAACTGG[C/T]ATCTTTCCAATCATC | 59349 |
rs114058403 | snp | C/T | 0.0026009 | 0.0359679 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202909101 | AACCAGATCCCTGCA[C/T]TGTAAACTACAGCGG | 59349 |
rs114068390 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894962 | TCAAAGACCACCTAG[A/G]AGTTTGCAAAAACAC | 59349 |
rs114132831 | snp | A/G | 0.00117296 | 0.0241889 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897011 | AGCATCCCTGGATGG[A/G]TAACTAGTCACAGGG | 59349 |
rs114170147 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | KLHL12 | GRCh38.p7 | 1:202927014 | AGGGAGACCAAGGAT[C/G]GGGGGTAGGGCCATA | 59349 |
rs114296224 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920886 | CATGAACATAACACT[A/C/G]GTCCGTGAACTTTTA | 59349 |
rs114381938 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907963 | ACCTAAACCCATCAG[C/T]GAGCAGCTTAATTAT | 59349 |
rs114442561 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901785 | GCTTTTGATAACTAT[A/G]AGAGCAACAGTGTTT | 59349 |
rs114602081 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930207 | CCTTGTTTTCAGGAT[A/G]TAAAATAGTACTTTA | 59349 |
rs114603931 | snp | C/G/T | 0.0119241 | 0.0764353 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890996 | CTAACATAGAAATAG[C/G/T]GGAACTAGTTGGCAA | 59349 |
rs114648613 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917553 | GTCCCTCCCTTCCAA[C/T]CGCTGCATCCTCACA | 59349 |
rs114652170 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928640 | TATATACTCTGCATC[A/G]TAATGGGCCCTGTCA | 59349 |
rs114687618 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908725 | AGAATCTAAATAATA[G/T]TGACAAAAAATTGTA | 59349 |
rs114698072 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925981 | GTGGTGATGCGCGCC[G/T]ATAATCCTAGCTACC | 59349 |
rs114725867 | snp | C/T | 0.00055364 | 0.0166287 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924941 | GTTCCACGGGTTTCA[C/T]TTGTGTGGGGCTAAT | 59349 |
rs114910242 | snp | A/G | 0.00218073 | 0.0329486 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892685 | AAGAAGCAAAAGAAA[A/G]AAATGAGTCAGCTGC | 59349 |
rs114950497 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920937 | AAGAAATTTCATGTT[C/T]GTAGAGGAGCCTGTG | 59349 |
rs114976163 | snp | C/T | 1.66205e-05 | 0.00288271 | missense | KLHL12 | GRCh38.p7 | 1:202894747 | CAGAGACATAGATCA[C/T]ATCTGCTCAGAATAA | 59349 |
rs114982865 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913957 | CACTATAGATATAGA[C/G]TACTTCCATCTTCAT | 59349 |
rs115044208 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923845 | CAATATCTACACTAA[C/G]ATGATAGAACTAACT | 59349 |
rs115074307 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911529 | TATTGGCCTTCGTTT[C/T]AGAATTTTTCCCATT | 59349 |
rs115165606 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905274 | AATGTACCTCCAAAG[A/C]ATCTTCTGGGTTTAC | 59349 |
rs115246010 | snp | A/C | 0.000181197 | 0.00951659 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918288 | CTCAGCTGCTTGCAT[A/C]AGGTCAACACAATTG | 59349 |
rs115289278 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920771 | AGGAATAAGTAATAG[A/G]TAACACCTTCCTGGA | 59349 |
rs115362249 | snp | A/T | 0.0535932 | 0.154675 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927267 | GACGTGATGACGCAA[A/T]GCAGCTGGAGCACCG | 59349 |
rs115401164 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908287 | GCTCAGATAAATTGA[C/T]ACCTTGCCCAACCAG | 59349 |
rs115536459 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914164 | GAGCAACTTGAAATC[A/C]TCCGAAGGTTTCAAG | 59349 |
rs115772063 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907931 | AAAATAAAATATAGC[A/G]GATAAATCACCATTC | 59349 |
rs115832268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911575 | GTCTTCTCTATAACT[C/T]TAAGGAAGGCAGGTG | 59349 |
rs115853273 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914023 | AAAAGAACTGGCAGC[C/T]TGAGGAAATGACTAG | 59349 |
rs115919082 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913887 | AGCTTCTCAGTTGCA[C/T]TAGCCACATTTCAAG | 59349 |
rs115925312 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB, missense | KLHL12 | GRCh38.p7 | 1:202927511 | ATCACGGCAAAACCC[C/G]GTTTCTACAAAAAAA | 59349 |
rs115969410 | snp | C/G | 0.0001188 | 0.00770623 | utr-variant-5-prime, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928551 | TTATTCACGTCCATT[C/G]TCCACAATGGCCTTT | 59349 |
rs116279845 | snp | G/T | 0.0168055 | 0.0901129 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905686 | CTATTTGCGCATCCC[G/T]AATTCAGAAACCCCA | 59349 |
rs116335033 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903104 | AAGTGAAGTTTCAGT[C/G]AACCAAGATCATGCC | 59349 |
rs116408835 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896027 | GGCACTGGGCTAAGA[C/G]ACTGATATCCTTCCA | 59349 |
rs116577545 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912177 | TGAAGAACATCACCT[A/G]AGAGATAATTTGAAC | 59349 |
rs116649176 | snp | A/T | 0.00126176 | 0.0250856 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895751 | GAGGTACAGAGCATT[A/T]CAGTTAGGCAAGTTT | 59349 |
rs116804728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896766 | TTATTAGGCTTTTCT[A/G]CTCTTAAGGCTGGAT | 59349 |
rs116873550 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917871 | AAATGTTTGTGAAAT[A/G]AGTGAACGGGTAATA | 59349 |
rs117012328 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902919 | GGGAGGATCACTTGA[A/G]TCCAGGAAGTGGACG | 59349 |
rs117038627 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904502 | TGGAGACCAATACTC[A/G]AACAATCTGACTCGT | 59349 |
rs117253520 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902642 | TATGAAACTTTTCCT[A/G]GTTGTTTTCTTAAAG | 59349 |
rs117441348 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905718 | ATCCAAAATGCTTCA[A/G]TGAGCATTTCCTTTG | 59349 |
rs117599971 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929020 | GTTTTTAATAGAGAC[A/G]GTGTTTCGCCATCTT | 59349 |
rs117610385 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925669 | GTTGCACAATAAATG[A/T]TTAGAATTTAATGTA | 59349 |
rs117657495 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912379 | AAGAGATGGCTAGTG[C/T]TTCATCCAGCCAAAG | 59349 |
rs117734978 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902784 | CACATGAACCCAGGA[A/G]ATCAAGACCAGCCTG | 59349 |
rs137879854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910973 | ACTCTGTGCCTACAT[C/T]AAAATACTCAATTTT | 59349 |
rs138126037 | in-del | -/CTTCTGACTTT | 0.190519 | 0.242821 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930390 | AGGAACTAGTTCAGA[-/CTTCTGACTTT]TTTCTTCTTTTATTT | 59349 |
rs138322968 | snp | A/C | 0.000938897 | 0.0216464 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894583 | TTCCTGCATCCCAGA[A/C]TCAATACCTAGACAG | 59349 |
rs138386822 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905589 | GTTGAGTAACCCTTA[C/T]CTGAAATGCTTACGA | 59349 |
rs138413674 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902006 | AAACATATAATATAC[A/G]TTTTTACTGCTAAAA | 59349 |
rs138663321 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917172 | TTAAGTCACTGAATG[C/T]CTGCCTGGCACAGGT | 59349 |
rs138894209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909768 | GGTTTCTCTCAAGGC[A/C]GTGACTCTACACGAT | 59349 |
rs138921137 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911663 | TTATCTAATGATCTC[C/T]AGGCTCACCCCTCAA | 59349 |
rs138996714 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893690 | CCCAACCCTTCTAAT[C/T]AGGAGAAAGGGAGGA | 59349 |
rs139091100 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928404 | GAGTTCCTCCCTACC[G/T]CTCACTAGGCAGGGC | 59349 |
rs139150651 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911987 | GCTCCAGGGGCTTTG[A/G]GTTTGTCACATATGC | 59349 |
rs139186973 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899205 | GAAATCCCAACTACT[C/T]GGGTGGCTCAGGCAT | 59349 |
rs139229189 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895453 | GCTCCTGCCAGACAA[C/T]AGGAGAGGTTAAAAA | 59349 |
rs139409896 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922038 | TGCATTTAATAATTA[C/T]GGTACTGAAATATGT | 59349 |
rs139515782 | snp | A/C | 0.00398564 | 0.0444627 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891503 | TGTGCTTCTAAAAGA[A/C]TGGGGCAGTAATCAG | 59349 |
rs139610755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918456 | TAGGATATATTCTTG[C/T]ATCTCAGCATCTTCT | 59349 |
rs139630242 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202895661 | ATAGCCACCAATGAC[A/G]TAGATCCGGTCATGA | 59349 |
rs139639243 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913370 | TTTCAGAGTGTCACT[A/G]TGAATAGATAAAAAA | 59349 |
rs139700374 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918713 | TATAAAACCAATTGC[A/G]AATTCAGCATAATGT | 59349 |
rs139765659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903034 | ACCATGGTGGCATAC[A/G]CCTGTAGTCCCAGCT | 59349 |
rs140329909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926901 | GGTATCGGAGAGGGG[A/C]AGTTCAGGGGGAGAG | 59349 |
rs140450656 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929253 | TCACACATTGTAGAG[A/T]AGAATGCAAGATTGG | 59349 |
rs140525542 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903615 | GTAGCTGGGACCACT[A/G]ATTTTTTTCTTTTCT | 59349 |
rs140526707 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908852 | TTGATTTATAGGAAA[G/T]AAAGCTTAGAGTGGT | 59349 |
rs140640368 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906608 | TAACATGAGTCAACT[C/G]TACATGTAAAAATGG | 59349 |
rs140690900 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905040 | GATGGGTAGAGGACA[C/T]GATGGTAAGAACAAT | 59349 |
rs140824666 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928609 | TCCTCTGAGCCTTAG[C/G]ATCCACAGACCTCAG | 59349 |
rs140880049 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896332 | CTAGGACTACAGGCA[A/T]GCACCACCATGCCTG | 59349 |
rs140963884 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202893283 | CACTGTGGCCCCTAC[A/G]TAGCATCGTGGAGTG | 59349 |
rs141073040 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925291 | TTTACAAATTAAGAA[A/C]CTAAGAGGCTTCCTC | 59349 |
rs141274078 | snp | A/G | 4.94662e-05 | 0.00497299 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202911057 | TGCACTACTTACCTC[A/G]GCATCTATTACATCT | 59349 |
rs141285295 | in-del | -/A/AA | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892095 | GTAGTTGTTCCTGGA[-/A/AA]AAAAAAAAAAAAGAC | 59349 |
rs141385656 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911923 | AGCTATTTTGAGCAA[C/T]GGGGAATGCTCACGG | 59349 |
rs141407975 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921886 | CCAAAAAGCACTCTC[G/T]ACCAAAGCCAAGAAC | 59349 |
rs141461319 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909393 | TCCCATCTATCGCAG[C/T]GCTTACATTTAACTA | 59349 |
rs141600848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900223 | TAACTCCCTGCCCCA[C/T]CCCCCAACCCCCCAA | 59349 |
rs141690187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897310 | CCATGATCTCGGCTC[A/T]CCACAACCTCTGCCT | 59349 |
rs141723953 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917753 | CTATATCTCTGTCTC[C/T]ACTAGCAGGTTGTGA | 59349 |
rs141979261 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898227 | TTCAAAGAGCAAAGT[C/G]TCTTTGAGAAAATCC | 59349 |
rs142097775 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895204 | AGAGATCAGCCTGGG[A/C]AACATGGCGAAACCC | 59349 |
rs142122234 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898829 | TCTGATTTGAACAAC[A/G]TAAGTACTCAAAAAC | 59349 |
rs142201030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899655 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 59349 |
rs142286273 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900846 | TCCAGCCTAGGTGAC[A/G]GAGCAAGACTCTGTC | 59349 |
rs142345049 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907864 | AGTGAACCGAGATCA[C/T]GCCACTGCACTCCAC | 59349 |
rs142462949 | snp | C/T | 0.110872 | 0.20771 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914805 | AGGAGGCAGAGATTG[C/T]GGTGAGCCGAGATCG | 59349 |
rs142501826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899206 | AAATCCCAACTACTC[A/G]GGTGGCTCAGGCATG | 59349 |
rs142770688 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911421 | GGGTTAAAAAAAAAA[A/T]ATATATATATACACA | 59349 |
rs142829708 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921296 | TCTCCTGCCTCAGCC[A/G]CCTGAGTAGCTGGGA | 59349 |
rs142856517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918517 | ACACCTAAGAAACAG[A/G]TTAGAAATTCTATGC | 59349 |
rs142916485 | snp | A/C | 0.0023933 | 0.0345097 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890941 | AATATTTTACTGATG[A/C]GAATCTCCAAAGTGT | 59349 |
rs142937097 | in-del | -/AAAC | 0.304438 | 0.244001 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923874 | TAAAAAAAAAACAAA[-/AAAC]AAACAAACAAAAAAC | 59349 |
rs143022231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894417 | AACTCTAAGAGAAAT[A/C]TGACATTATGCTTAT | 59349 |
rs143253111 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900653 | TGGATCACTTGAGGT[C/T]AGGAGTTCAAGGCCA | 59349 |
rs143506051 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910270 | TTGGGATTTCAGGCC[C/T]GAGTCTGGTTCCAGA | 59349 |
rs143551175 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929302 | TTGGAAATATTCGTC[A/G]ATTTTAATAAAATTT | 59349 |
rs143609770 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917424 | TGCCATGTTGCCCAG[A/G]CTAGTATCAAACTCC | 59349 |
rs143845290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899434 | TCACACATAAACCAC[A/G]GAGTTTTTCTAAGAG | 59349 |
rs143896042 | in-del | -/AAAC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923875 | AAAAAAAAAACAAAA[-/AAAC]AACAAACAAAAAACT | 59349 |
rs143989383 | snp | C/G | 0.000461893 | 0.0151899 | missense | KLHL12 | GRCh38.p7 | 1:202894596 | GACTCAATACCTAGA[C/G]AGTAGATCACTCCAC | 59349 |
rs144002280 | snp | C/T | 0.000153988 | 0.00877328 | missense | KLHL12 | GRCh38.p7 | 1:202918235 | AGAATGAACTCTTCA[C/T]GCTGTACCACTTCAG | 59349 |
rs144193954 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913448 | AAGTTCATTCATTTG[A/C]GGGCTTTACTGAACC | 59349 |
rs144275185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922829 | GCTAGTAAGAGACAG[A/G]TATCATTCTTATTAA | 59349 |
rs144315235 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894883 | AATGAGATAAGTCAA[G/T]TAAGTTTTATAGACA | 59349 |
rs144464549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902541 | AACTCTTTTAGTACA[A/T]GGTTATAATATTCTT | 59349 |
rs144476575 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909225 | TCTGACTACAGAAAA[A/C]CAGTTTGCAAAGCCC | 59349 |
rs144569049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907161 | TAGTAGAAAATACCA[C/T]CTACAATGCCCTATC | 59349 |
rs144654237 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927445 | CCCGGCACTTTGGCA[G/T]GCCGAGGCGAGCGAA | 59349 |
rs144674526 | in-del | -/CA | 0.413416 | 0.189196 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924859 | AATCTGCCAAAACAT[-/CA]CACTGTAAAAATTCA | 59349 |
rs144773467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921033 | TCCCCTTTGTTGAGA[G/T]AGGGTCTTGCTCTGT | 59349 |
rs144875412 | snp | C/G | 0.00193447 | 0.0310402 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928439 | AGAGAGAATTCCAAC[C/G]CTTAATATGCCAAGC | 59349 |
rs144901203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926203 | CTTACACTTGCTTAA[A/G]ATATTGAAGCTCTTC | 59349 |
rs145163563 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900504 | GCAGTGAACAAGGTC[A/G]TGTTCCTGCACTCCA | 59349 |
rs145227005 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900060 | GTGTGATCCTTCTAT[A/C]CAAACACATTTCCCA | 59349 |
rs145298894 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903483 | TTTCTTTTTTGAGAC[A/G]AGGTCTTGCTCTGCT | 59349 |
rs145422767 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903782 | CATGCGTCACCATGC[C/T]TGGCTAATTTTTATA | 59349 |
rs145544079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896588 | AAATGTGCTAGGAAT[C/T]ATACAGACAGCTTAG | 59349 |
rs145663074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922093 | TCATTCAATAAACTA[C/T]ATTTCCATCAAATAG | 59349 |
rs145732400 | snp | C/T | 0.102726 | 0.202016 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904016 | TATCTATCTATCTAT[C/T]TATCTATCTATCTAT | 59349 |
rs145763155 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916116 | TTTTGGCTATGCCTG[C/T]CACTTCAGCACAAGG | 59349 |
rs145790799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901712 | CAGATCCTGTGTTTT[A/G]ACAGACTGTCTACCA | 59349 |
rs145856179 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919230 | CACTGTGCTCTAATC[C/T]GGGTGACAGAGTGAG | 59349 |
rs145899041 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905312 | CAAAAATTTTCATTA[A/G]CTTTTAGTTCAATTT | 59349 |
rs146009954 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917927 | TTACTTCCAATTTCT[A/G]CTTATTCTATACTCT | 59349 |
rs146048593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918593 | TCAGCAAGACCTTTA[A/C]ACCTGTCTCTGCTTA | 59349 |
rs146098295 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921470 | GTGAGCCACCATGCC[C/T]GGCCCTTAGACTGCA | 59349 |
rs146104148 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911411 | TAGTCAATTTGGGTT[-/A]AAAAAAAAATATATA | 59349 |
rs146339370 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912899 | GCAAAAAACTCGAGG[A/G]CTGTATTTGTGACTA | 59349 |
rs146374291 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898883 | AAAATTACACAAACA[C/T]GTGAGAATAAGGAAT | 59349 |
rs146435055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896010 | TCCTTTCTCTTCCAT[A/G]AGGCACTGGGCTAAG | 59349 |
rs146495812 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897117 | ATAAGGCTGTCGAAT[A/G]GGGAGTTATTTTTCC | 59349 |
rs146510757 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892768 | GATTGCTTAAGCCCA[C/G]GAGGGAATTTGAGAC | 59349 |
rs146558988 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913882 | AAATCAGCTTCTCAG[C/G/T]TGCATTAGCCACATT | 59349 |
rs146563271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893510 | CGGTCACTAATGACT[A/C]GCTGAGTTCTACAGT | 59349 |
rs146603910 | snp | A/G | 0.0252325 | 0.109451 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928968 | TCCGAGTAGCTGGGA[A/G]TACAGGTGCACACCA | 59349 |
rs146629149 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909361 | AAATGATATAAACAG[A/G]TATGTTGAGCAGTAT | 59349 |
rs146660695 | snp | A/G | 0.000395315 | 0.0140535 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918312 | ACAATTGTGGGTTTC[A/G]GCAAAATCCCTAATA | 59349 |
rs146750755 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202909056 | CTGACTCCGAAGTTC[A/G]GGCCTCAGATGAAAC | 59349 |
rs146751785 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929239 | AAACTGTCCCTGACT[C/G]ACACATTGTAGAGAA | 59349 |
rs146773681 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908166 | TGATATCTGAGTATT[C/T]AGTGTGTGCCAGCTA | 59349 |
rs147035573 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897711 | ATGTTGAAACTTAGG[A/G]TCCAAGTGATGGATT | 59349 |
rs147064793 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900253 | AAAATAAATATATAT[A/G]TCTAAAGAAGTCAGG | 59349 |
rs147096150 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915467 | AGGGCAGTCTTGACA[A/C]ACACTTAAAAAAAAA | 59349 |
rs147225487 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906577 | GTTACAGAGATTGAT[G/T]GTATAACAATGTATT | 59349 |
rs147287870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922542 | CCCAGGCTGGAGTGC[A/C]GTGGCGTGATCTGGG | 59349 |
rs147466780 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894509 | GGGAAGTCTATGAAC[A/G]TCATTTTGGTAAAAA | 59349 |
rs147585347 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915928 | GTAAGTGTTCAACAA[G/T]TATTTAGTAAGTGAA | 59349 |
rs147604185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903553 | CAGCCTCAGCCTCGA[C/T]CTCCTGGGCTCAAGC | 59349 |
rs147627650 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900080 | CACATTTCCCATGTA[C/G]ATGAATATGCCAGCA | 59349 |
rs147899668 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897241 | TTCTTTTTTTTTTTT[A/T]TTTTTTTTTTGGAGA | 59349 |
rs148026596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917709 | TAGGCTCACTATTCT[C/T]ATGATCCTCTTTATA | 59349 |
rs148035458 | snp | G/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929710 | TGTTCAGAGCCTGGT[G/T]CGGTGGTGTACACCT | 59349 |
rs148088850 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927888 | TCAGGAGGCTAATGC[A/G]GGAGAATCGCTAGAA | 59349 |
rs148209811 | snp | C/T | 0.199254 | 0.244796 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920533 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 59349 |
rs148332426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921629 | TATATTTAGTCTAAA[C/T]TGTTAGTAGTATATC | 59349 |
rs148372216 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900818 | GCAGTGAGCAGAGAT[C/T]GCACCACTGCACTCC | 59349 |
rs148387479 | in-del | -/CAA | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926449 | TATAGATAATTCCTC[-/CAA]CAACTCTGCAAGACC | 59349 |
rs148595476 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919246 | GGGTGACAGAGTGAG[A/T]CTCTGTCTCAAAAAC | 59349 |
rs148619648 | snp | A/C/G | 4.94404e-05 | 0.00497173 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919864 | TTCCATGGTAGAGGC[A/C/G]GTCAAACCTTGGATG | 59349 |
rs148742366 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907287 | CTACATTGAACATGC[A/G]GTACTTATGCCATTA | 59349 |
rs148773696 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895110 | AAAGGAGTATTTGTC[A/G]GCTGGGCACAGTGGC | 59349 |
rs148784887 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914280 | AAGAGGTTAGATGCT[G/T]CTCTGGTACATTAGG | 59349 |
rs148859334 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924439 | TCCCTCTGGTATTCA[C/T]TTAAAAATTTTTAAA | 59349 |
rs148880605 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896592 | GTGCTAGGAATTATA[C/T]AGACAGCTTAGAAAG | 59349 |
rs149144776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900601 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCACAGC | 59349 |
rs149238988 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902540 | TAACTCTTTTAGTAC[A/T]TGGTTATAATATTCT | 59349 |
rs149277577 | in-del | -/A | 0.352721 | 0.227922 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893092 | CTGTCTCTAAAAAAT[-/A]AAAAAAAATCTAATA | 59349 |
rs149312594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917365 | GACCACAGGTGCTCA[C/T]CACCATGCCAGGCTA | 59349 |
rs149390078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927165 | GGCGCGGGGCTAGCA[A/G]GCGGCTCGGGAGGAG | 59349 |
rs149481464 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914932 | GAAGAAAGAAATCTG[C/T]AACTGATTGTGGTCA | 59349 |
rs149546791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920973 | TAACTCCAGTCTCTC[C/T]AGGACTACCTAGTTC | 59349 |
rs149652791 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894832 | AATTTTCCAAGGGTC[C/T]TTTAAAAGTCTGAGA | 59349 |
rs149693591 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891805 | GCGAAAGACCTCGGG[A/G]AAATAAAAAGATCCT | 59349 |
rs149715559 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906882 | GGCCAGGCTGGTCTC[A/G]AACTACTGACCTCAA | 59349 |
rs149746176 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896559 | CAGTTCAGTTTAACA[C/T]AGCACGACCAATGAA | 59349 |
rs149769020 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904004 | TATGTATCTATCTAT[C/G]TATCTATCTATTTAT | 59349 |
rs149844399 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918790 | AAGAAAAGGAGAAGA[C/T]AGTAATAACAAATCT | 59349 |
rs149905455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928413 | CCTACCGCTCACTAG[A/G]CAGGGCAGGCAGAGA | 59349 |
rs150275818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898378 | GAGCAAATGTAGTAC[C/T]TTGAAGCTGACAGGA | 59349 |
rs150359643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202927018 | AGACCAAGGATGGGG[C/G]GTAGGGCCATAACCC | 59349 |
rs150484500 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911420 | TGGGTTAAAAAAAAA[A/T]TATATATATATACAC | 59349 |
rs150495472 | snp | A/T | 0.000153988 | 0.00877328 | missense | KLHL12 | GRCh38.p7 | 1:202918177 | AATCCGTACCTGAAT[A/T]TCGTCGCACTTGATT | 59349 |
rs150501317 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895606 | CCTCATCTGCTGTGT[A/G]GTCTAGACATTCCAC | 59349 |
rs150540118 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902300 | CCAGACATGGTAGCA[C/T]ATGCCTGTAATCTCA | 59349 |
rs150678183 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202891048 | AAGAGACAGGAGCTA[C/T]GGCTGATCCCTACAT | 59349 |
rs150758735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911951 | CGGACTGTGTGGTAA[G/T]GAGAGACCCAAACAC | 59349 |
rs150836202 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921957 | TTTTGAAAAAACATA[C/T]TAGGTTTTATTAACA | 59349 |
rs150943407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924839 | AAGTGGTAGATCTTA[G/T]CCAGAATCTGCCAAA | 59349 |
rs151227476 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899682 | AATACAAAAATTAGC[C/T]GGGTGCAGTGATGCG | 59349 |
rs151239266 | snp | A/G | 6.58946e-05 | 0.0057396 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202911108 | TAGGGGCATCCGCAC[A/G]TACTGTAGCAGGTTA | 59349 |
rs151291403 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914830 | AGATCGTGCCATTAC[A/T]CTCCAGCCTGGGCGA | 59349 |
rs180717568 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923856 | CTAAGATGATAGAAC[C/T]AACTAAAAAAAAAAC | 59349 |
rs180825075 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911431 | AAAAATATATATATA[C/T]ACACACACACATATA | 59349 |
rs180861769 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901754 | AGTAATTAACTTCCC[C/T]GCAACTGCCAACAGA | 59349 |
rs180908361 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920114 | AGGTCAGGAATTCAA[C/G]ACCAGCCTGGCCAAC | 59349 |
rs180959892 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930539 | TGGGTATCCATCCCC[G/T]CAAGCGTTTATCCTT | 59349 |
rs181122437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899782 | GAGCCGAGATTGCAC[C/T]ACTGCACTCCAGACT | 59349 |
rs181151163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911771 | CTGCCTGTGGACGCC[A/G]CCGAAGAAGCATCTT | 59349 |
rs181205485 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930175 | TTAATTAAATTAAAT[A/T]AAAAGTAAAAATAAT | 59349 |
rs181305009 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906884 | CCAGGCTGGTCTCGA[A/T]CTACTGACCTCAAGT | 59349 |
rs181390364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913355 | ATTCTGGGAGATACC[G/T]TTCAGAGTGTCACTG | 59349 |
rs181592608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895220 | AACATGGCGAAACCC[C/T]ATCTCTACTAAAAAT | 59349 |
rs181824999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896110 | AAGAACCTTAAAAGG[C/T]AGGAGGGTTGGATTT | 59349 |
rs181828312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914054 | AAGGCTAGTGTAGCA[A/G]AGTGAATGAGGGTGA | 59349 |
rs181859485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923380 | CTCATGGAGAACAGT[A/G]TAGGACAGGGATCTG | 59349 |
rs181880779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913751 | AGTTAGCCAGGGGGA[A/G]TAAGAGAGTACTCCG | 59349 |
rs182015665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901080 | CCCCTCTCTTTCTTG[A/G]TATGATTTCATTCAG | 59349 |
rs182024343 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919308 | ACAAACCACCTGTAA[C/T]CCTGTGAAAATATCA | 59349 |
rs182107621 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927935 | TGCTGAGCCGAGATC[C/G]CGCCATTGCACTCCG | 59349 |
rs182320559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912428 | AAACTTTGGTTTGGT[C/T]GTGGAGGTGGTTTCG | 59349 |
rs182427470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902945 | GGACGCTGCAGTGAG[C/T]CAAAATCATGCCATT | 59349 |
rs182434629 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920920 | TAAGACACAATATTT[C/G]AAAGAAATTTCATGT | 59349 |
rs182613620 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904176 | AGCCCGGCTAATTTT[G/T]TATTTTTAGTAGAGA | 59349 |
rs182824633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908889 | ACTTGTCTGAGATGA[C/T]AGAAGAAAAGGTCTG | 59349 |
rs182866786 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890997 | TAACATAGAAATAGC[A/G]GAACTAGTTGGCAAA | 59349 |
rs182898170 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922392 | CTAACATGGTGAAAC[C/T]CCGTCTCCACTAAAA | 59349 |
rs182910818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897024 | GGGTAACTAGTCACA[A/G]GGAAGTGTCAACAGA | 59349 |
rs182914986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916071 | AGATATTCTAGTGAA[C/T]TGCCAGTTTCCAAGT | 59349 |
rs183166166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916871 | TCCAGCTACACAGGA[A/G]GATGAGGTGGGAGAG | 59349 |
rs183168544 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914588 | GACTAATCAAATGGG[C/T]TGGGCGTGGTGGCTC | 59349 |
rs183179124 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912635 | AGCTCTGGGCCCCTA[C/T]GGCGGTGGAGGCCAA | 59349 |
rs183217173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926023 | GGCCCGAGAATCACT[A/T]GAACCCAGGAGGTGG | 59349 |
rs183416870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896369 | TTTTTTGTTTACTTT[C/T]TTGTAGAGACAGAGT | 59349 |
rs183424384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903406 | GTAGCCAGCTTTACT[G/T]GCCCTTCTGCGAACT | 59349 |
rs183430901 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922059 | TGAAATATGTAAGTA[C/T]ATGTATTCCAGAAAT | 59349 |
rs183441153 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907374 | TGGGAGGCCAAGGTG[A/G]GTGGATCAATTGCAG | 59349 |
rs183465315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911441 | ATATATACACACACA[C/T]ATATATATATATGTA | 59349 |
rs183663100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894487 | ACACACCAGGGTTTT[A/C]GTTGAAGGGAAGTCT | 59349 |
rs183670774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913115 | CTTCAAGGAACTACT[A/G]TGTATTACGCACTAT | 59349 |
rs183944432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908090 | TATAAAATGTTTTTA[A/T]ACACTATACACCTAG | 59349 |
rs184089247 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904659 | GAACAGTGTGAAAAA[C/G]CACATTTCTAAAACT | 59349 |
rs184096157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922772 | ATTACAGGCGTGAGC[C/T]ACCACGCCCAGCTGA | 59349 |
rs184146425 | snp | A/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930292 | GGAACTTAATAATAA[A/G]AGAGGCTTTGTTTAG | 59349 |
rs184599585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900422 | AGGTGTGATGGCAAA[C/T]GCCTGTAGTCCCAGC | 59349 |
rs184608213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918923 | TGTCAATTATGTATA[C/T]ATAAAAACTGAAAAC | 59349 |
rs184617386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897541 | ACTGCACCATTTCAA[C/T]CTATTGAGATGACTG | 59349 |
rs184684820 | snp | A/G | 1.65759e-05 | 0.00287883 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894736 | ATCAAAGCCTCCAGA[A/G]ACATAGATCATATCT | 59349 |
rs184831901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913676 | TTCCTAGTTTAGACT[G/T]GTGAGGCAAGGAAGG | 59349 |
rs184857519 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892385 | ACGACGGGGAGTATG[C/T]GTCAAATAAGTACAA | 59349 |
rs184972717 | snp | A/G | 0.000912507 | 0.0213406 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918418 | GGCAGCAAACACTTT[A/G]GAATAGTTGGACAGG | 59349 |
rs185074162 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899307 | ATAAGGCAAAACTCC[A/C]TCTCAAAGAAAAAGC | 59349 |
rs185085735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905300 | TTTACTGATTCACAA[A/C]AATTTTCATTAGCTT | 59349 |
rs185108985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924119 | TATTCAACACAATAT[A/G]TTCAGCAGCCTTACT | 59349 |
rs185223623 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909907 | GTTTCTCTGAACTTG[C/T]GCCTTTGTAAACAGC | 59349 |
rs185229945 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929738 | CCTACCTGTTGTCCT[A/G]TCTGCTTTGGAGACT | 59349 |
rs185405309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896272 | GTTCACTGCAACCTC[A/G]AACTCCTGGGCTCAA | 59349 |
rs185416566 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914107 | GGAGAGTTAAGCAAG[G/T]GCCAGGTACAGAGAG | 59349 |
rs185432602 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907182 | ATGCCCTATCTAAAA[A/G]TTCTCTTTTTAAAAA | 59349 |
rs185620746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910856 | CAGATTTTCATTTGT[G/T]TCAAGAGCCTGACTT | 59349 |
rs185626950 | snp | A/G | 0.0130921 | 0.0798413 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928904 | GCGCGATCTCAGCTC[A/G]CTGCAACCTCCGCCT | 59349 |
rs185738739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912865 | GAGACATGTTTTAGA[C/T]AAATACTCATGTGTA | 59349 |
rs185744873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923276 | AATTAGCAATCAGCC[A/G]TTCTAGTTCATTTCT | 59349 |
rs185790901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920464 | TCACTGCAAGCTCCA[C/T]CTCCTGGGTTCATGC | 59349 |
rs185911520 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902263 | GGTGAAACCCCATCT[A/C]TAGTGAAAATACAAA | 59349 |
rs185915150 | snp | A/T | 3.2962e-05 | 0.00405954 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895596 | CAGACCCCATCCTCA[A/T]CTGCTGTGTAGTCTA | 59349 |
rs185921723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913856 | ATTCACCGTAATTAA[A/C]ACTAAATTAAAAATC | 59349 |
rs185971663 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902983 | AGTGACACAGTGAGA[C/T]CTTGTATCAAAACAA | 59349 |
rs185979577 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921037 | CTTTGTTGAGATAGG[G/T]TCTTGCTCTGTTCCC | 59349 |
rs186035640 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906228 | GAGGCTGAGGTGGGC[A/G]GATCACCTGACGTCA | 59349 |
rs186402841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919396 | CTTAATGGCCAGATA[G/T]ATAAAGAGTATCCAT | 59349 |
rs186418640 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912210 | TTTGGAAAAACGGAA[A/G]TGATTGAAATCATGA | 59349 |
rs186424131 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923471 | AGGTTCCTGTTTTCC[C/T]TACTAGCCATGTGAC | 59349 |
rs186652147 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912443 | CGTGGAGGTGGTTTC[A/G]GTTGGCATGACAGCC | 59349 |
rs186787715 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928043 | CCAGCACTTTGGGAG[A/G]CCGAGACGGGTGGAT | 59349 |
rs186816403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907705 | GAGTCCAGGAGTTCA[A/C]GACCCAGCCTGGGCA | 59349 |
rs186858543 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911924 | GCTATTTTGAGCAAT[G/T]GGGAATGCTCACGGA | 59349 |
rs186909056 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908299 | TGATACCTTGCCCAA[C/T]CAGTCATTGCTGGGG | 59349 |
rs187144078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901133 | AAAGAAGTAGAAAGG[A/C]AATAGATTATATTAA | 59349 |
rs187249478 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897194 | TAAAACTCTAGAAAG[C/G]AAACTTCAACATGAC | 59349 |
rs187258543 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916259 | TGGAAAATAATTCCT[C/T]TACAGTTGGAACCAA | 59349 |
rs187374297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926113 | CTGTCTCAAAAAAAA[A/C]AAAAAAAAAAGAAAC | 59349 |
rs187499505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922394 | AACATGGTGAAACCC[C/T]GTCTCCACTAAAAAT | 59349 |
rs187718841 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917235 | TCTTCCCCCGCAAGA[A/G]ACAGGGTCTCCCTCT | 59349 |
rs187744102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904456 | TCTTCCCCAGAAGAA[C/T]TCCTAAGGTTTTAAT | 59349 |
rs187758880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893166 | TCTTGTCTCTGTCCA[A/G]AAATGAGGATCAGAT | 59349 |
rs187767000 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912877 | AGACAAATACTCATG[A/C/T]GTATGGGCAAAAAAC | 59349 |
rs187956805 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896633 | AGTGGTGGCCATCTG[A/G]GTTTACCTTGACACA | 59349 |
rs188001859 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898107 | CAGGGTCTTGCTATA[A/T]TGCCCAGGCTGGTCT | 59349 |
rs188044530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913235 | AAAAAAACCTACACT[A/G]CATCACTGGAAGGAC | 59349 |
rs188061337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906324 | GCCAGGCGTGGTGGC[A/G]CACACCTGTAATCCC | 59349 |
rs188106067 | snp | A/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930512 | ATGTGTACTAATCAC[A/G]TCACAGAAAGTTGGG | 59349 |
rs188135970 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927562 | CCGCACCGCGCCTGT[A/G]GTCCCAGCTACTCGA | 59349 |
rs188247358 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914615 | GCTCACGCCTGTAAT[C/G]TCAGCACTTTGGGAG | 59349 |
rs188310210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910909 | GAAATATGCTTGGGG[A/T]CTACCCAGCACCACT | 59349 |
rs188381579 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929816 | AACGTAGCAAGAGCA[C/T]GCCTCAAAATATATT | 59349 |
rs188508213 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912639 | CTGGGCCCCTATGGC[A/G]GTGGAGGCCAATACT | 59349 |
rs188583551 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911768 | TTTCTGCCTGTGGAC[A/G]CCGCCGAAGAAGCAT | 59349 |
rs188760993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903420 | TTGCCCTTCTGCGAA[C/G]TGTACACTCAAATCT | 59349 |
rs188784016 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891501 | CATGTGCTTCTAAAA[G/T]AATGGGGCAGTAATC | 59349 |
rs188888124 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928965 | CTCTCCGAGTAGCTG[A/G]GAGTACAGGTGCACA | 59349 |
rs188969547 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900819 | CAGTGAGCAGAGATC[A/G]CACCACTGCACTCCA | 59349 |
rs188977957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918981 | GGGGACCAGGAACGG[C/T]GGCTCGTGCCTATAA | 59349 |
rs189051856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922121 | TAGTTTAAATATGGA[A/T]ACAATTTCACTATGT | 59349 |
rs189056712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894535 | AAAAAGGAATCCTTA[C/T]CCACAGCCCATTACC | 59349 |
rs189217666 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904747 | GTGTGCTGTGACACG[C/T]TGTTAGAGAAATAAG | 59349 |
rs189358114 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919436 | GTATAGTATCACTTT[G/T]TTATTATATTTCCTT | 59349 |
rs189583958 | snp | C/T | 0.431916 | 0.171483 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899651 | TCTAACATGGCAAAA[C/T]CCCGTCTCTACTAAA | 59349 |
rs189630517 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901645 | GGGATCCTTCGATCA[A/C]TGATTCCCAAACTTC | 59349 |
rs189666976 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923559 | ATAAAATTCATACTT[C/T]GGAGGCTAAGGCGGC | 59349 |
rs189867790 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918643 | CAAGATGAATCACAT[C/T]CAGAGACCTGGCACA | 59349 |
rs190046090 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912331 | ATCCTACGAATGGCC[A/C/G]TAACTGTGAAGTTAG | 59349 |
rs190121321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910769 | GGAGAAGGGGACAAA[A/G]TTTATTATCAAGTGT | 59349 |
rs190158820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913722 | AACAAATTGAAATCT[C/G]ATGGATGAGTAGCAG | 59349 |
rs190159194 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902719 | TTTGAGCCAGGCATG[A/G]TGGCTCACACCTGTA | 59349 |
rs190204303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923324 | GTGACACTCTCTTTA[A/C]CCAGTTAAATTCCAA | 59349 |
rs190288612 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927849 | TAGCCGGGCGTTGTG[C/G]CACGCGCCTGTAATC | 59349 |
rs190397858 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895208 | ATCAGCCTGGGCAAC[A/G]TGGCGAAACCCCATC | 59349 |
rs190414117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905480 | AAGTTACTAGAGTGA[A/G]TGTCGGAAATTGGAG | 59349 |
rs190432313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903211 | ACATAAGGTGACTTT[C/T]TGAAGCTGTTACCAA | 59349 |
rs190443048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921857 | TTTTTATTTCTCCAT[C/T]AGCCAGAGAATAACC | 59349 |
rs190684322 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907193 | AAAAGTTCTCTTTTT[A/T]AAAAAATGCAGTATC | 59349 |
rs190701475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925806 | CATATCTGGATTTCT[C/T]CTTAAAATGAAACTT | 59349 |
rs190705922 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896360 | CTGGCTAATTTTTTT[A/G]TTTACTTTTTTGTAG | 59349 |
rs190964368 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914220 | TGTTTTGTAAAGATT[A/T]TCCTGGCTACTGTGG | 59349 |
rs190989004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916013 | TGTAGTGCTCATTCT[A/G]TTCATTGTATTTTCC | 59349 |
rs191075002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895887 | AAATAGCTACCTACT[C/G]AACGAAATGCCTGTT | 59349 |
rs191084141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913942 | CGGGAGCAAACCAGA[C/T]ACTATAGATATAGAG | 59349 |
rs191227918 | snp | A/C/T | 4.94338e-05 | 0.00497141 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896831 | TAACATCCCTCCCAA[A/C/T]GAATGGTTTCACCAT | 59349 |
rs191264287 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912572 | GGCAACTACAATAAT[A/C]AGTCTTCAAATTTTG | 59349 |
rs191373421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908491 | TGAAGCACACAGAGG[G/T]TAAGGTTCCTGCCCA | 59349 |
rs191483990 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920904 | CCGTGAACTTTTAAG[A/G]TAAGACACAATATTT | 59349 |
rs191587514 | snp | A/T | 0.00697358 | 0.0586358 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928451 | AACGCTTAATATGCC[A/T]AGCATCTGATTGCAG | 59349 |
rs191634083 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909814 | GTTCTAGTAACCACT[C/T]CTCAACCTTGTCCCT | 59349 |
rs191757819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911981 | CCAAGTGCTCCAGGG[A/G]CTTTGGGTTTGTCAC | 59349 |
rs191762153 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927363 | AGCGCGGGGCTTCTG[C/T]ACGCTGCTAGGAAGC | 59349 |
rs191859078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904471 | CTCCTAAGGTTTTAA[C/T]GTTTTAACCCTAAGT | 59349 |
rs191862961 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922400 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 59349 |
rs192018117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907992 | ATCAACTAACACCTT[A/G]GCACGCATCATGAGT | 59349 |
rs192131278 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904854 | GAGACAGCCACAAAT[C/T]AGAAAAGTAATTTCC | 59349 |
rs192276450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898778 | AGACTGAAAAGAGAC[A/G]TGAAATCACGAGCAA | 59349 |
rs192330698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894477 | ATATATTAAGACACA[C/G]CAGGGTTTTAGTTGA | 59349 |
rs192337463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913019 | CACCCATGCTGTTGA[C/T]TGCTAAATGTAATAG | 59349 |
rs192571382 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918690 | TATAAAACTCTTGGG[A/T]ATCAAACTATAAAAC | 59349 |
rs192587680 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897509 | GATTACAGGTGTGAG[G/T]CACTGTGCCCGGCAA | 59349 |
rs192594955 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916815 | GAGACCCCATCTCAA[C/T]AAAAATTTTAAAAAA | 59349 |
rs192698600 | snp | C/T | 0.000164745 | 0.00907442 | missense | KLHL12 | GRCh38.p7 | 1:202918209 | GCTTTTCCACCTCTC[C/T]TTGACTCAGAAGAAT | 59349 |
rs192877710 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891959 | TGACCTCCAAAAGAA[C/G]TGTCAGATGAGTCTC | 59349 |
rs193013397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922220 | TTACTACTATTTCAT[C/G]TGATTCTCACAGCAA | 59349 |
rs193052760 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929374 | CAAGATTGTTAACTG[C/T]AGCATTGTTTGTAGA | 59349 |
rs193088815 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912698 | TGGTGGTTTCAGTAG[C/T]AGCAGTAGCTATGGC | 59349 |
rs193126170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910828 | ACAGACAGCAAAACA[C/T]AAAATTGAACCACAG | 59349 |
rs193207242 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903771 | GGGATTACAGGCATG[C/T]GTCACCATGCCTGGC | 59349 |
rs199552913 | snp | A/C/T | 0.000165113 | 0.00908466 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897000 | TGGGTTAGTTCAGCA[A/C/T]CCCTGGATGGGTAAC | 59349 |
rs199553895 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923874 | CTAAAAAAAAAACAA[A/C]AAACAAACAAAAAAC | 59349 |
rs199693719 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202911093 | ATACCTGGGGGTTAG[C/T]AGGGGCATCCGCACA | 59349 |
rs199701457 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895188 | TGAGCTCAGGAGTTA[-/A]GAGATCAGCCTGGGC | 59349 |
rs199715266 | snp | A/G | | | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919798 | AAGCAGTTCTTGTAC[A/G]TTCTCCACTGTCACA | 59349 |
rs199764415 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917454 | CTGGACACAAGCAGT[C/T]CTGCCTCAGCCTCCC | 59349 |
rs199766178 | snp | A/C | | | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927107 | CGCTCCCGAACCCAC[A/C]CAGCCGCACCGGGCC | 59349 |
rs199832892 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923867 | GAACTAACTAAAAAA[A/C]AAACAAAAAACAAAC | 59349 |
rs199923464 | snp | C/T | 8.23825e-05 | 0.00641751 | missense | KLHL12 | GRCh38.p7 | 1:202911083 | CATCTGTGATATACC[C/T]GGGGGTTAGTAGGGG | 59349 |
rs199942378 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926070 | AGATCACACCACTGC[A/C]CTCCAGCCTGGGCAA | 59349 |
rs200004276 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911418 | TTGGGTTAAAAAAAA[-/T]AATATATATATATAC | 59349 |
rs200041248 | snp | C/T | 0.00199792 | 0.0315431 | missense | KLHL12 | GRCh38.p7 | 1:202894599 | TCAATACCTAGACAG[C/T]AGATCACTCCACTGG | 59349 |
rs200100201 | snp | C/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928823 | GTGAGCCCTTTGATT[C/T]TTTTTTTTTTTTTTT | 59349 |
rs200107292 | snp | A/G | 6.60426e-05 | 0.00574604 | stop-gained, intron-variant | KLHL12 | GRCh38.p7 | 1:202895555 | CAGCAAGACCTCGTC[A/G]GACATTCATAGGGGC | 59349 |
rs200140675 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924862 | CTGCCAAAACATCAC[-/A]CTGTAAAAATTCAAA | 59349 |
rs200154578 | snp | A/G | 9.88647e-05 | 0.00703012 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896832 | AACATCCCTCCCAAC[A/G]AATGGTTTCACCATT | 59349 |
rs200231184 | snp | A/C | 0.000884372 | 0.0210096 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919711 | ATTTTCAACCTTTCC[A/C]GGGCTATTTTGACAT | 59349 |
rs200246888 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892097 | GGAAAAAAAAAAAAA[C/T]ACTTGGATTTTACCA | 59349 |
rs200261542 | in-del | -/T | 0.277867 | 0.248442 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912989 | GGGTTTTAATGCAGA[-/T]TTTTTTTTTTTTGGC | 59349 |
rs200319952 | snp | C/T | 3.29652e-05 | 0.00405974 | missense | KLHL12 | GRCh38.p7 | 1:202919874 | GAGGCAGTCAAACCT[C/T]GGATGTCAACATAAG | 59349 |
rs200334208 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895419 | AACATTTGACCTTAA[-/T]TTTTTCTCCGTATTT | 59349 |
rs200356503 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896997 | AGATGGGTTAGTTCA[A/C/G]CATCCCTGGATGGGT | 59349 |
rs200385208 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905466 | CTTGTCCAAACAGCA[A/G]GTTACTAGAGTGAGT | 59349 |
rs200428678 | snp | A/C | 3.29489e-05 | 0.00405874 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918330 | AAAATCCCTAATACC[A/C]AGGCAATTAGAAGGG | 59349 |
rs200454104 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904370 | ATAATTTTGTATATG[A/T]TTTTTTTATTTATTC | 59349 |
rs200539451 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911454 | CACATATATATATAT[A/G]TATCTCTCTCTCTCT | 59349 |
rs200592020 | in-del | -/TTG | 0.0295035 | 0.117819 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924236 | TTTTCCTAATTCCCT[-/TTG]TTAAGTGCTTATGAG | 59349 |
rs200638058 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923869 | ACTAACTAAAAAAAA[A/C]ACAAAAAACAAACAA | 59349 |
rs200644118 | snp | C/T | 0.000115882 | 0.007611 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911018 | AAGGTAAGAGTCCGT[C/T]AAGGTTTTGGATCCT | 59349 |
rs200666052 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892336 | TTTTTCCTGGAATAT[C/T]TGTTACCCACCCTTC | 59349 |
rs200729559 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897228 | GCACCATTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 59349 |
rs200732718 | in-del | -/ATT | 0.0189856 | 0.0955633 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906145 | TTTTTAAAAATAATA[-/ATT]ATTTTTTAAAAAACA | 59349 |
rs200760291 | in-del | -/TATT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904013 | ATCTATCTATCTATC[-/TATT]TATCTATCTATCTAT | 59349 |
rs200771973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925301 | AAGAACCTAAGAGGC[C/T]TCCTCAGACCCAAAC | 59349 |
rs200862656 | snp | A/C | 0.000330617 | 0.012853 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918398 | TCACACCTAGGACAG[A/C]CACAGGCAGCAAACA | 59349 |
rs200919739 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912511 | CGATAATGGATTTGG[C/T]AATGATGGAAGCAAT | 59349 |
rs200970568 | snp | A/G | 0.000115311 | 0.00759224 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894622 | TCCACTGGCCACTAC[A/G]AGTCCGGCACCTTCC | 59349 |
rs201020193 | snp | C/T | | | stop-gained | KLHL12 | GRCh38.p7 | 1:202911162 | CTTGGCATGCTTCAC[C/T]CAGTTGATGACAGCC | 59349 |
rs201067798 | in-del | -/CTG | 0.495056 | 0.049474 | cds-indel | KLHL12 | GRCh38.p7 | 1:202892336 | TTTTTCCTGGAATAT[-/CTG]TTACCCACCCTTCTC | 59349 |
rs201079639 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893092 | TCTGTCTCTAAAAAA[A/T]AAAAAAAATCTAATA | 59349 |
rs201124654 | snp | G/T | 1.64738e-05 | 0.00286995 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918279 | GCTAAAAACCTCAGC[G/T]GCTTGCATCAGGTCA | 59349 |
rs201154267 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919516 | CTCCATTTTTTTTTT[-/A]AAACAGAAAAGGTGC | 59349 |
rs201375357 | snp | A/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892083 | ATGTAGTTGTTCCTG[A/G]AAAAAAAAAAAAAGA | 59349 |
rs201410647 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899833 | ATCTCAAAAAAAAAA[A/T]AAAAAAATAATAATA | 59349 |
rs201444078 | snp | C/G/T | 0.000231399 | 0.010754 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202893385 | ACCATCAAATCCCCC[C/G/T]ACCACATAAATATGG | 59349 |
rs201457975 | snp | A/C | 1.6531e-05 | 0.00287493 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908960 | CTATGTTGTCACCTG[A/C]AAGAAGTAGTTGAAA | 59349 |
rs201463752 | snp | C/T | | | missense | KLHL12 | GRCh38.p7 | 1:202911154 | CGCTCTTTCTTGGCA[C/T]GCTTCACCCAGTTGA | 59349 |
rs201540872 | snp | A/G | 0.00123653 | 0.0248342 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896988 | GCAGAAAAAAGATGG[A/G]TTAGTTCAGCATCCC | 59349 |
rs201544123 | snp | C/T | | | missense | KLHL12 | GRCh38.p7 | 1:202925027 | GCACAATCCGATGGG[C/T]AGGGAAGTCTTTCTG | 59349 |
rs201586617 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924860 | ATCTGCCAAAACATC[A/T]CACTGTAAAAATTCA | 59349 |
rs201652933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925450 | CACTTGACATTTAAT[A/G]TGATCAATGCTGAAA | 59349 |
rs201678661 | snp | G/T | 0.000741015 | 0.0192343 | missense | KLHL12 | GRCh38.p7 | 1:202925037 | ATGGGCAGGGAAGTC[G/T]TTCTGCTCTACTCTC | 59349 |
rs201727753 | snp | C/G/T | 0.0010419 | 0.0228008 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893196 | TCACATAGACTCTTG[C/G/T]TCTGGCTACATATTG | 59349 |
rs201737922 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911458 | TATATATATATGTAT[C/G]TCTCTCTCTCTCTCT | 59349 |
rs201757174 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911417 | TTTGGGTTAAAAAAA[-/T]AAATATATATATATA | 59349 |
rs201795698 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202896932 | CTGGCTTCCAAAGCC[C/T]CCAACCACCAAAAGC | 59349 |
rs201914130 | snp | A/G | 0.00299544 | 0.0385843 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910984 | ACATTAAAATACTCA[A/G]TTTTGAATACATAAC | 59349 |
rs201991684 | snp | A/G | | | missense | KLHL12 | GRCh38.p7 | 1:202894201 | GAACGCTTGGTGGCC[A/G]TTGGTGTAACATTAG | 59349 |
rs202025633 | snp | C/G | 6.60993e-05 | 0.0057485 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892524 | CTCTGGATGGTGCTC[C/G]AACAATGGTCACTTC | 59349 |
rs202140389 | snp | A/C/G | 0.000411993 | 0.014347 | missense, synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918183 | TACCTGAATTTCGTC[A/C/G]CACTTGATTAGCTTT | 59349 |
rs367673080 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925764 | TTCTAAAGAAGTATC[C/T]AAATGATATGTCTGA | 59349 |
rs367759347 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921533 | TCCTAAGGGACTTTC[C/T]TATGTAACATCATCT | 59349 |
rs367782840 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896208 | AACTTTTTTTTTCTG[A/C]GTTGGGATCTCACTA | 59349 |
rs367799153 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917683 | CTTCTATGTAATGTC[C/T]TTACTTTGTATAGGC | 59349 |
rs367807794 | snp | A/G | 8.2763e-05 | 0.00643231 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911016 | CTAAGGTAAGAGTCC[A/G]TCAAGGTTTTGGATC | 59349 |
rs367825125 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907100 | TGTTGATATGTATCT[A/G]TGTATAAAGCATATG | 59349 |
rs367836231 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900544 | ACAGAGTGAGAACTT[C/G]TCTCAAAAAATAAAA | 59349 |
rs367866588 | snp | C/T | 1.66164e-05 | 0.00288235 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893398 | CCCACCACATAAATA[C/T]GGTCATTCAGCAGGG | 59349 |
rs367964739 | in-del | -/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896204 | ACAAACTTTTTTTTT[-/C]CTGAGTTGGGATCTC | 59349 |
rs368003835 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914151 | GATTTGACTCTCAGA[A/G]CAACTTGAAATCATC | 59349 |
rs368086460 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917343 | CCTCAGCCTCTCAAG[G/T]AGCTGGGACCACAGG | 59349 |
rs368388082 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916616 | ACCACTGCACTCCAG[A/C]CTGGAAGAAGTATAC | 59349 |
rs368473168 | in-del | -/AAAAAAA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926117 | CTCAAAAAAAAAAAA[-/AAAAAAA]GAAACTTCAATTGAG | 59349 |
rs368623850 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925762 | TTTTCTAAAGAAGTA[C/T]CCAAATGATATGTCT | 59349 |
rs368645767 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898941 | ATTCTAGATGTGGCA[C/G]AATTTTTTTTCCTTA | 59349 |
rs368688314 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924942 | TTCCACGGGTTTCAT[G/T]TGTGTGGGGCTAATT | 59349 |
rs368758054 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913192 | CTAAGCATACATATG[A/G]CCAATTAGATAATGT | 59349 |
rs368994742 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929119 | CAGGCGTCAGCCACA[A/G]CGCCTAGCCCTTTGA | 59349 |
rs368996814 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910877 | AGCCTGACTTGCCAA[A/G]AAATTCGCTTTTCTT | 59349 |
rs368997746 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920395 | TTTTTTTTTTTTTTT[G/T]AGACGGAATCTTGCA | 59349 |
rs368999167 | in-del | -/A/AA | 0.499104 | 0.0211472 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928274 | GCAAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAG | 59349 |
rs369037621 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899869 | TAAAAAAATCAAAGC[A/C]TAAGAATGAAGGGTT | 59349 |
rs369092945 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922632 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCAC | 59349 |
rs369147094 | snp | A/G | 3.36231e-05 | 0.00410005 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894783 | TTACAGACTATTAGA[A/G]AATGAGAGATTTCTA | 59349 |
rs369345390 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900467 | ACATGGGAGGATCAC[G/T]TAAGTCCAGGAGGTT | 59349 |
rs369386479 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909774 | TCTCAAGGCAGTGAC[C/T]CTACACGATTCTCTT | 59349 |
rs369522096 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929268 | AAGAATGCAAGATTG[A/G]TATATTATTGGGGGC | 59349 |
rs369527541 | snp | C/T | 8.80011e-05 | 0.00663271 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894278 | ATTCAAGCCGTCATA[C/T]CCTCCTGGAAGACAG | 59349 |
rs369566671 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927422 | GAATGGTGGCTCACG[C/T]CTATAATCCCGGCAC | 59349 |
rs369572265 | snp | C/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929580 | AGACAAAGTGGTAAC[C/G]TTGGTTTCTTTGGGG | 59349 |
rs369665720 | snp | A/G | 4.94376e-05 | 0.00497156 | missense | KLHL12 | GRCh38.p7 | 1:202894650 | TCCCGGGCTGTCTGC[A/G]TATCTCCCAGCATGC | 59349 |
rs369722994 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926091 | GCCTGGGCAACAGAG[C/T]GAGACTCTGTCTCAA | 59349 |
rs369738191 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900924 | GTGGTGTGCATTTTG[A/T]AGTCCCAGCTACTCC | 59349 |
rs369775438 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899830 | TCCATCTCAAAAAAA[A/T]AAAAAAAAAATAATA | 59349 |
rs369987689 | in-del | -/TACTGCTAAAAAAC | 0.0298908 | 0.118541 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902011 | TATAATATACATTTT[-/TACTGCTAAAAAAC]TTGGAAAATACAGAC | 59349 |
rs370074115 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894478 | TATATTAAGACACAC[C/T]AGGGTTTTAGTTGAA | 59349 |
rs370079441 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916182 | ATTTTAGCAAATTCT[C/T]GACTCAATAGCATTT | 59349 |
rs370220269 | snp | C/T | 0.000421354 | 0.0145086 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924932 | ACAACTAGAGTTCCA[C/T]GGGTTTCATTTGTGT | 59349 |
rs370333116 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907771 | AAATTAGCCAGGCAT[G/T]GTGGCACGTGCCTGC | 59349 |
rs370397228 | snp | A/T | 3.29538e-05 | 0.00405904 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202909023 | ACCTAGGCGAGCCCT[A/T]GTCCTGGGTCCCTGC | 59349 |
rs370563669 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914183 | GAAGGTTTCAAGCAG[G/T]CTAGTGATATGATCA | 59349 |
rs370636005 | snp | A/G | 3.52858e-05 | 0.0042002 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925210 | TTGGATTCTGCAACT[A/G]CAAGAGGGAAAAAAA | 59349 |
rs370712373 | in-del | -/AAAAAA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904831 | ACTGATCTTTAGTTC[-/AAAAAA]AAAAAAGGAGACAGC | 59349 |
rs370821592 | in-del | -/A/AA/AAA | 0.300421 | 0.244863 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892083 | TGTAGTTGTTCCTGG[-/A/AA/AAA]AAAAAAAAAAAAAGA | 59349 |
rs370906064 | snp | A/C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902334 | ACTCGGGAGGCTGAG[A/C/G]CAGGAGAATCGCTTG | 59349 |
rs370915927 | snp | C/G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924481 | AAAAAGGCTGGATGC[C/G/T]GTGGCTCACACCTGT | 59349 |
rs370921211 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920446 | CAGTGGTGCCATCTC[A/G]GCTCACTGCAAGCTC | 59349 |
rs370985224 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897072 | TTGTTTTATGTGGCT[A/G]AGGGATGCAATCCGA | 59349 |
rs371045468 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900521 | GTTCCTGCACTCCAG[C/T]CTGGGGAACAGAGTG | 59349 |
rs371123761 | snp | C/T | 1.66065e-05 | 0.00288149 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924961 | GTGGGGCTAATTTAC[C/T]ACTTACCTCACTAGT | 59349 |
rs371357554 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898689 | AAATTCTACAGGTCG[A/C]ACAGCTTGGCTTCTT | 59349 |
rs371497376 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899037 | TTCAAAATAGCCTGG[A/G]TGCAGTGGCTCATGC | 59349 |
rs371606294 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910019 | GCTCTAATTAAATGG[C/T]ACCTCTATTAACCTG | 59349 |
rs371632039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895256 | AATATAGCTGGGCAT[A/G]GTGGTGCATGCCTGT | 59349 |
rs371649452 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893466 | ATGTATGGTACTAAG[C/T]CTAGAATCTGAATTA | 59349 |
rs371734371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922638 | ACTACAGGCGCCCGC[C/T]ACCACGCACGGCTAA | 59349 |
rs371809978 | snp | A/C | 1.6557e-05 | 0.00287719 | missense | KLHL12 | GRCh38.p7 | 1:202894728 | CTGCTTCCATCAAAG[A/C]CTCCAGAGACATAGA | 59349 |
rs371825905 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920578 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 59349 |
rs371891349 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904896 | TTTGAGACAGTAATG[C/G]GTAAGGTTAATAACT | 59349 |
rs371894274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922196 | AGAATTTTTCAGCAT[A/G]CTTCTCATTTACTAC | 59349 |
rs372009814 | snp | A/G | | | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927161 | GTGCGGCGCGGGGCT[A/G]GCAGGCGGCTCGGGA | 59349 |
rs372025668 | snp | A/G | 0.000838474 | 0.0204581 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928466 | AAGCATCTGATTGCA[A/G]CAAGTATGTTTTACC | 59349 |
rs372193695 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915919 | GGGCACACAGTAAGT[G/T]TTCAACAAGTATTTA | 59349 |
rs372203321 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903013 | AACAAACAAATGAAA[C/T]AGATCACCATGGTGG | 59349 |
rs372238532 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925860 | CCTGTAATCCCAGCA[C/T]TTTAGGAGGCTGAGG | 59349 |
rs372318969 | snp | C/T | | | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918204 | GATTAGCTTTTCCAC[C/T]TCTCCTTGACTCAGA | 59349 |
rs372382040 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913964 | GATATAGAGTACTTC[C/G]ATCTTCATAGAATGT | 59349 |
rs372386980 | snp | A/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930214 | TTCAGGATGTAAAAT[A/G]GTACTTTAATGATAT | 59349 |
rs372411839 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920396 | TTTTTTTTTTTTTTG[A/T]GACGGAATCTTGCAC | 59349 |
rs372445477 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922473 | TAAAGGGTCTAAAGA[A/T]CAAAGAAGATCCAAG | 59349 |
rs372451033 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900922 | TGGTGGTGTGCATTT[G/T]GTAGTCCCAGCTACT | 59349 |
rs372468701 | snp | C/T | 3.29799e-05 | 0.00406065 | missense, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892543 | AATGGTCACTTCTCG[C/T]GGAGAACACAAACAC | 59349 |
rs372482197 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900123 | ATGAATAAAAATTCC[C/T]ACACCAACCAAGAGG | 59349 |
rs372557154 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895133 | ACAGTGGCTCACACC[G/T]GTAATCCCAGCACCT | 59349 |
rs372619245 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916214 | CAACAGCAGCTTCTC[C/T]GGGCTGATACAGAGC | 59349 |
rs372649208 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914565 | GGTTTTTTAGTTTGC[A/G]TTTTTAAGACTAATC | 59349 |
rs372676266 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905843 | AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 59349 |
rs372811933 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899476 | TATGTACTTGCCAAA[C/T]AAAGTGGACCCTCTC | 59349 |
rs372876948 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202893277 | CCGAAGCACTGTGGC[C/T]CCTACATAGCATCGT | 59349 |
rs372880162 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915150 | GTACTGGCGTTCTTA[C/T]TTTATGCTCAGAACA | 59349 |
rs372935694 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905968 | CGCCACCACACCTGG[C/T]TTTTTTTTTTTTTTT | 59349 |
rs372986075 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919718 | ACCTTTCCAGGGCTA[C/T]TTTGACATAAACAAT | 59349 |
rs373065951 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919391 | TACCACTTAATGGCC[A/G]GATAGATAAAGAGTA | 59349 |
rs373118930 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895570 | GGACATTCATAGGGG[A/C]CACAGAATACCAGAC | 59349 |
rs373159355 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895212 | GCCTGGGCAACATGG[C/T]GAAACCCCATCTCTA | 59349 |
rs373415245 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912121 | CCAGGTGCTCACTTA[A/G]CTGTGAAAAAGATAT | 59349 |
rs373418244 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927149 | TGTGGGGATGGAGTG[C/T]GGCGCGGGGCTAGCA | 59349 |
rs373543513 | snp | C/G/T | 9.01354e-05 | 0.00671272 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895754 | GTACAGAGCATTTCA[C/G/T]TTAGGCAAGTTTTGG | 59349 |
rs373564360 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902741 | ACACCTGTAACCCTA[A/G]CACTTTGGGAGGCCA | 59349 |
rs373607101 | snp | C/G | 5.30997e-05 | 0.00515238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893474 | TACTAAGCCTAGAAT[C/G]TGAATTATAGAAATA | 59349 |
rs373726100 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900524 | CCTGCACTCCAGCCT[C/G]GGGAACAGAGTGAGA | 59349 |
rs373745471 | snp | A/G | 0.000166995 | 0.00913617 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909175 | GATACCTGTAATACT[A/G]TAAGAGTACAAAGAG | 59349 |
rs373842247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907865 | GTGAACCGAGATCAC[A/G]CCACTGCACTCCACC | 59349 |
rs374067043 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911525 | CACGTATTGGCCTTC[A/G]TTTCAGAATTTTTCC | 59349 |
rs374092817 | in-del | -/ACAA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910073 | TGGAAAGGAAAACAA[-/ACAA]TAAATAGTAGTAAAC | 59349 |
rs374123386 | snp | A/G | 1.68131e-05 | 0.00289935 | missense, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202925197 | ACAAAATGGGTCCTT[A/G]GATTCTGCAACTACA | 59349 |
rs374141096 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921307 | AGCCGCCTGAGTAGC[C/T]GGGACTACAGGCACA | 59349 |
rs374143058 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896167 | TTCATTCAGCACTGA[C/G]AGACATGCTGAGGGA | 59349 |
rs374159511 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898095 | GGCTTTTGGAGACAG[C/G]GTCTTGCTATATTGC | 59349 |
rs374183317 | snp | A/G | 0.000350482 | 0.0132332 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918432 | TAGAATAGTTGGACA[A/G]GTGTGATCTAGGATA | 59349 |
rs374330933 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899841 | AAAAAAAAAAAAAAA[A/T]AATAATAATAAATAA | 59349 |
rs374454606 | in-del | -/GTT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924238 | TTCCTAATTCCCTTT[-/GTT]AAGTGCTTATGAGTT | 59349 |
rs374574961 | snp | C/T | 0.000155988 | 0.00883004 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894312 | CCATTCCAGAAAGAG[C/T]GGTAAATCCTCATGC | 59349 |
rs374654325 | snp | A/T | 8.27917e-05 | 0.00643343 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911011 | TAACACTAAGGTAAG[A/T]GTCCGTCAAGGTTTT | 59349 |
rs374702624 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915316 | ACATCCTGCTTCCCA[C/T]TGTTTTAAGTACTAT | 59349 |
rs374707184 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903203 | ACTTTGAGACATAAG[A/G]TGACTTTTTGAAGCT | 59349 |
rs374744903 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924856 | CAGAATCTGCCAAAA[C/T]ATCACACTGTAAAAA | 59349 |
rs374959824 | snp | A/T | 1.66255e-05 | 0.00288314 | missense | KLHL12 | GRCh38.p7 | 1:202894749 | GAGACATAGATCATA[A/T]CTGCTCAGAATAAAC | 59349 |
rs375291812 | snp | A/G | 9.89658e-05 | 0.00703371 | synonymous-codon, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202925166 | AATGCCTCCCATAAA[A/G]CAGTGCGGAGAAAGA | 59349 |
rs375332591 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927519 | AAAACCCCGTTTCTA[A/C]AAAAAAAAAAAAAAA | 59349 |
rs375339122 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916950 | TGCACTCCAGCCTGG[A/G]TGACAGAGTGAGACC | 59349 |
rs375381660 | snp | G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928956 | TGCCTCAGCCTCTCC[G/T]AGTAGCTGGGAGTAC | 59349 |
rs375406326 | snp | C/T | 1.73531e-05 | 0.00294555 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893243 | TAAATCCTCACCCTG[C/T]AATTGCATAGAGTCT | 59349 |
rs375431121 | in-del | -/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901474 | TTTTTTTTTTTTTTT[-/T]AATTTTTTAAAGAGA | 59349 |
rs375442358 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899696 | CCGGGTGCAGTGATG[C/T]GCACCTGTAGTCTCA | 59349 |
rs375473818 | snp | A/G | 0.00372926 | 0.04302 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892701 | AAATGAGTCAGCTGC[A/G]TGCAGTGGCACGTGC | 59349 |
rs375492449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905084 | CACTGACAAAGCGAT[A/G]CTAAGAATCTAATTG | 59349 |
rs375587779 | snp | C/T | 0.000155988 | 0.00883003 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894150 | AAGGTCTGACAGCAT[C/T]GCCTATTGTCCCCTC | 59349 |
rs375687177 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900923 | GGTGGTGTGCATTTT[G/T]TAGTCCCAGCTACTC | 59349 |
rs375809629 | in-del | -/A | 0.488424 | 0.0751925 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927981 | GAGACTCTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 59349 |
rs375880693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912399 | TCCAGCCAAAGAAGT[C/T]GAAGTGGTTCTGGAA | 59349 |
rs375897923 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920369 | GCTCTATTTTGTTGG[A/T]TTTTTTTTTTTTTTT | 59349 |
rs375961099 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898717 | CTTCAAGAAATAAAC[C/T]GGCTGGGAAAAACCA | 59349 |
rs376063159 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925987 | ATGCGCGCCTATAAT[A/C]CTAGCTACCAAGAAG | 59349 |
rs376114815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907062 | TCATAGTTTTTCACC[A/G]TTCAGTCCTTCAATC | 59349 |
rs376123224 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918273 | CTTCTGGCTAAAAAC[C/T]TCAGCTGCTTGCATC | 59349 |
rs376280169 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892342 | CTGGAATATCTGTTA[C/T]CCACCCTTCTCAGGA | 59349 |
rs376286456 | snp | C/G | 4.94474e-05 | 0.00497205 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202895586 | CACAGAATACCAGAC[C/G]CCATCCTCATCTGCT | 59349 |
rs376469895 | snp | C/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929882 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCTAAC | 59349 |
rs376590960 | snp | A/T | 0.000943841 | 0.0217032 | missense, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928497 | TTCCAGGTACTGAGG[A/T]ACTTTTTGACATCGA | 59349 |
rs376678688 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914737 | CAGGTGTGGTGCGCA[C/T]GCCTGTGGTCCCAGC | 59349 |
rs376706008 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910054 | AAGAAGTTCTTAGTC[A/G]AACTGGAAAGGAAAA | 59349 |
rs376725676 | snp | C/T | 6.59022e-05 | 0.00573993 | missense | KLHL12 | GRCh38.p7 | 1:202894638 | AGTCCGGCACCTTCC[C/T]GGGCTGTCTGCATAT | 59349 |
rs376799807 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902405 | ATTGCCCTCCAGCCT[C/G]GGTAACAGAGCGAGA | 59349 |
rs376806380 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910939 | TCTCACTGGCATTCC[C/T]AGAGAGGCAAAACAG | 59349 |
rs376818182 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923886 | CAAAAAACAAACAAA[A/C]AACTTGTGCTTAAAA | 59349 |
rs376898815 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912977 | CATTCCAACAAAGGG[C/T]TTTAATGCAGATTTT | 59349 |
rs377079678 | snp | A/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930400 | TCAGACTTCTGACTT[A/T]TTTCTTCTTTTATTT | 59349 |
rs377115026 | snp | C/T | 1.68977e-05 | 0.00290665 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924918 | TTCAGTGAAATTAGA[C/T]AACTAGAGTTCCACG | 59349 |
rs377116039 | snp | A/C/G | 0.0178377 | 0.0929631 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905954 | GAACTACAGGTGCCC[A/C/G]CCACCACACCTGGCT | 59349 |
rs377128800 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927322 | GTCACGTGAGGAGGT[A/G]GTGTCACGTGACCTG | 59349 |
rs377158170 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911807 | TCTCTCTCCTCCCTG[A/C]CGTCATGTCTAAGTC | 59349 |
rs377347301 | in-del | -/A | 0.0588605 | 0.161139 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923860 | ATGATAGAACTAACT[-/A]AAAAAAAAAACAAAA | 59349 |
rs377508625 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922289 | AGAGATAAAGGGGGG[C/G]CGGGCACATGGCTCA | 59349 |
rs377534020 | snp | A/T | 1.6477e-05 | 0.00287024 | missense, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892586 | GCTGGGTTCCCATGG[A/T]TGTCACGACTTCCCA | 59349 |
rs377582913 | snp | C/T | 0.000445798 | 0.0149232 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908978 | GAAGTAGTTGAAAAG[C/T]ATCCCCTCATTCTGC | 59349 |
rs377622258 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910186 | CTATTATCATCCCTG[G/T]TTTACACATAAGAAA | 59349 |
rs377624127 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902305 | CATGGTAGCACATGC[C/T]TGTAATCTCAGCTAC | 59349 |
rs377653358 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923993 | TGCACCCACAACTGA[A/G]CTTTGAAAAAATAAA | 59349 |
rs377719791 | snp | A/T | 1.83764e-05 | 0.00303115 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895761 | GCATTTCAGTTAGGC[A/T]AGTTTTGGGCCTTAC | 59349 |
rs386369351 | in-del | -/CAAA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923882 | AAACAAAAAACAAAC[-/CAAA]AAAAAACTTGTGCTT | 59349 |
rs386638572 | in-del | AC/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899650 | GTCTAACATGGCAAA[AC/T]CCCGTCTCTACTAAA | 59349 |
rs397724843 | in-del | -/T | 0 | 0 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928847 | TTTTTTTTTTTTTTT[-/T]GAGACGGACTCTTGC | 59349 |
rs397762149 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903470 | TCTTGTTTTTTTTTT[-/T]CTTTTTTGAGACAAG | 59349 |
rs397808894 | in-del | -/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900922 | TGGTGGTGTGCATTT[-/T]GTAGTCCCAGCTACT | 59349 |
rs397862729 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897251 | TTTTTTTTTTTTTTT[-/T]GGAGACAGAGTTTCG | 59349 |
rs397982670 | in-del | -/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903185 | TATGTCTCAAAGTAA[-/T]TTTTTTTTTTTTTTT | 59349 |
rs398074576 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900921 | GTGGTGGTGTGCATT[-/T]TGTAGTCCCAGCTAC | 59349 |
rs398089816 | in-del | -/C | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927292 | CACCGCCCTCCCCCC[-/C]GCTCCAGAGTCTGCG | 59349 |
rs527439123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911582 | CTATAACTTTAAGGA[A/T]GGCAGGTGGGGGAAT | 59349 |
rs527440505 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911881 | GGAGGGTTGAGCTTT[C/G]AAATAACCAATGAAG | 59349 |
rs527451285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903743 | TTCTCCTGCCTCAAC[C/T]TCCCCAATAGCTGGG | 59349 |
rs527647877 | snp | C/T | 0.000922296 | 0.0214545 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202909026 | TAGGCGAGCCCTTGT[C/T]CTGGGTCCCTGCATC | 59349 |
rs527784206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915513 | CTCAAGCTGTTTTTC[A/T]TTTAAGCTTCTAAAT | 59349 |
rs527821267 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914780 | TGAGGCAGGAGAATC[C/G/T]TTTGAACCCAGGAGG | 59349 |
rs527925216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895470 | GGAGAGGTTAAAAAC[C/T]CTGGTCCAGCCACAG | 59349 |
rs528046454 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905960 | CAGGTGCCCGCCACC[A/C]CACCTGGCTTTTTTT | 59349 |
rs528048909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913147 | CTATTTGAGAAGATA[C/T]ATTTAATTAATCATC | 59349 |
rs528318422 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892111 | AGACTTGGATTTTAC[C/T]AAGTTTACTTAAACT | 59349 |
rs528411121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899103 | AGATCACTTGAGGTA[A/G]GGAGTTTGAGACCAG | 59349 |
rs528539548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897876 | TGCCTGGCCTAAAAT[A/C]TCTTTTCCATGAACA | 59349 |
rs528965776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901577 | AAAGTGCTGGGATTA[C/T]AGACATGAGCCACTG | 59349 |
rs528981267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893874 | GAAGGTAAGTAGCTA[C/T]TCTTTTGTCCTTATG | 59349 |
rs529002768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900889 | AACACAAATACAAAC[A/C]CAAAAATTAGCCAGG | 59349 |
rs529068196 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915582 | ATTCCAAAGCCTGTA[C/T]AGTTCCAAAAGAAAT | 59349 |
rs529083611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922580 | CCAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 59349 |
rs529133020 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930160 | AAATAAATAAATAAA[C/T]TAATTAAATTAAATA | 59349 |
rs529203549 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906066 | CCTCGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 59349 |
rs529357865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892793 | TGAGACCAGCCTGGG[C/T]AACATGGTGAGACCC | 59349 |
rs529406607 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908058 | ACCACCCCATACATA[C/G/T]AGAGTAATTCATAAC | 59349 |
rs529431844 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895734 | TATGGATTTGGAGAG[A/C]AGAGGTACAGAGCAT | 59349 |
rs529461041 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913996 | CTATTGAACAGCTCT[-/G]TTCTACAGCAAAAAA | 59349 |
rs529538834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914509 | TCTAGGTTAAATTAG[A/G]TATATCAATTTAAAG | 59349 |
rs529793267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924445 | TGGTATTCACTTAAA[A/C]ATTTTTAAACTTTAG | 59349 |
rs529919619 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912926 | ACTAATTGTGTAACA[A/G]GTTATTTTAGTTTCT | 59349 |
rs529931840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904566 | AGAAGCCTGTTTGTT[C/T]TCTGCCAATGATGGA | 59349 |
rs529974984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919071 | CCTGAGCAACATAGA[A/G]AGAACTCATCTCCAC | 59349 |
rs530070458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910841 | CACAAAATTGAACCA[C/T]AGATTTTCATTTGTG | 59349 |
rs530164577 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926662 | GTCTTCCTTCTAGGG[G/T]ATTCCTGCCTCAACA | 59349 |
rs530223709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899268 | AGTGAGCTGAGATAG[C/T]GCCACTACACTCCAG | 59349 |
rs530247877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916418 | CAGCATTTTAGGAGG[C/T]TGAAGTGGCTGATGT | 59349 |
rs530342844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895809 | GTTGTATCTGCACAC[C/G]TCTCTGCTTCTTCAC | 59349 |
rs530404779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896491 | CTACCACGCCCAGCC[C/T]AAACTTCTGAGCTCA | 59349 |
rs530463333 | snp | A/G | 8.23825e-05 | 0.00641751 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918350 | AATTAGAAGGGTCCA[A/G]CTGACTTTCTAAGAA | 59349 |
rs530616039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906732 | AATGGTGCAATCTTG[G/T]CTCACTGCAACCTCC | 59349 |
rs530619827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921321 | CTGGGACTACAGGCA[C/T]ATGCCACCATGCCTG | 59349 |
rs530691425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892833 | AAAATTTAAAGAAAG[A/G]AAGAAAGAAATTAGC | 59349 |
rs530774625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926909 | AGAGGGGCAGTTCAG[A/G]GGGAGAGTTGAGAGG | 59349 |
rs530847755 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892213 | ACATATGAGGCACAA[C/T]ATACATATAGTACAC | 59349 |
rs530935328 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902464 | CAAACAAACAAAAAA[A/G]CCTACAAATGTGACC | 59349 |
rs531014497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927354 | CTGTACCCTAGCGCG[C/G]GGCTTCTGTACGCTG | 59349 |
rs531048195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898029 | ATTCTGACAGCCTTT[A/G]TATCTTCCCCTTCCC | 59349 |
rs531091315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912539 | AATTTTGGAGGTGGT[G/T]GAAGCTACAGTGATT | 59349 |
rs531136755 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919842 | TGTACACAAAGTCCA[A/G]TAAAATTTCCATGGT | 59349 |
rs531222115 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912329 | CCATCCTACGAATGG[C/T]CATAACTGTGAAGTT | 59349 |
rs531369099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909908 | TTTCTCTGAACTTGC[A/G]CCTTTGTAAACAGCT | 59349 |
rs531404224 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924169 | TCAGGCAATTACTAA[C/G]TAGTGTTTCTTAATA | 59349 |
rs531407538 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916517 | GGTGTAGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 59349 |
rs531537260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923195 | GAAAAAAAGAATTCA[C/T]TTCCAAATAACAAAA | 59349 |
rs531573088 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914627 | AATCTCAGCACTTTG[A/G]GAGGCCGAGGCGGGT | 59349 |
rs531741096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901676 | TTTGCTGTGAAGGAC[C/T]CTCTTCATTATTTTT | 59349 |
rs531799358 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929092 | CCTTGGCCTCCTAAA[G/T]TGCTGGGATTACAGG | 59349 |
rs531871526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921201 | TTTTTTTTTGACACA[A/G]TCTTGCTCTGTTGCC | 59349 |
rs531872714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901064 | TAAAATAAAGAAAAA[A/C]CCCCTCTCTTTCTTG | 59349 |
rs531872797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908945 | GAGTATTATTTTCAA[C/T]TATGTTGTCACCTGC | 59349 |
rs531942809 | in-del | -/TT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915124 | TCACAAAGAATTCTC[-/TT]GAGTATTAGGTACTG | 59349 |
rs531956679 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920924 | ACACAATATTTCAAA[G/T]AAATTTCATGTTCGT | 59349 |
rs532057953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915439 | ACTTGCTTTCTTTCC[A/T]GAAAAAAAGCAAAGG | 59349 |
rs532093823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912048 | TGCAAGGCCACACAA[A/G]GTGGATGGAAGAGTT | 59349 |
rs532123750 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904776 | AGGCAGATGCAGGAC[C/T]GCTAAAATAACAGGG | 59349 |
rs532129678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898930 | GTGATAATGGCATTC[C/T]AGATGTGGCAGAATT | 59349 |
rs532145573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918491 | ATGTTATCAGATGAA[A/C]CCTTGTTTCAACACC | 59349 |
rs532295855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905524 | AAGCAAAATGTCTTA[C/T]CTCCTAGTGCCAGGT | 59349 |
rs532500718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904232 | TGGTCTCAAACTCCC[G/T]ATCTCAGGTGATCCA | 59349 |
rs532640887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903548 | CACTGCAGCCTCAGC[C/G]TCGACCTCCTGGGCT | 59349 |
rs532727076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925320 | TCAGACCCAAACATA[C/T]ACAAGTTGAGGGCAC | 59349 |
rs532874656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897172 | TGAAACTTAAATTTC[C/T]GGACATTAAAACTCT | 59349 |
rs532908531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907238 | TTATGGATGATTTTT[A/G]TTTATTTTTTGCTTC | 59349 |
rs533004323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892855 | GAAATTAGCCTTCTA[C/T]TCCTTTCCACACAAG | 59349 |
rs533129821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927400 | ACAAAAAGGTCGGGT[A/G]GGCAGGGAATGGTGG | 59349 |
rs533131028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922060 | GAAATATGTAAGTAC[A/G]TGTATTCCAGAAATT | 59349 |
rs533165554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927150 | GTGGGGATGGAGTGC[A/G]GCGCGGGGCTAGCAG | 59349 |
rs533180381 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930017 | AGTCATGGTGGCCTG[C/T]GCCTGAAATCCCAGC | 59349 |
rs533183714 | in-del | -/TTC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908595 | CACACTGGGCTCCTT[-/TTC]TTCCTCTCTTCATTC | 59349 |
rs533274717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893747 | AGATGGAGGGAAAGG[A/G]GTTGTGATTATGGTT | 59349 |
rs533353301 | in-del | -/TCA | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926699 | GTCTCAGCATATCCT[-/TCA]TCCTCACCCTTCTGA | 59349 |
rs533484363 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202891128 | CTCGGCATTTGAGAC[C/T]GTTGATTTTTAATAT | 59349 |
rs533516688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916770 | CATTGCTTGAGCCTA[C/G]CAGTTCAAGACCAGC | 59349 |
rs533530152 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906760 | TCCGCCTCCCGGGTT[C/G]AAGCGATTCTCCTGC | 59349 |
rs533678490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913420 | GATACTCTAAAAACG[C/G]AGATGTTTCACAAAG | 59349 |
rs533936518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896094 | GATGAGGATTTATTA[C/T]AAGAACCTTAAAAGG | 59349 |
rs534027321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900484 | AAGTCCAGGAGGTTA[A/C]GGCTGCAGTGAACAA | 59349 |
rs534064181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907787 | GTGGCACGTGCCTGC[A/G]GTCCCAGCTACTTGG | 59349 |
rs534109291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922249 | AACCTGGTAAGGTAG[C/T]TAGGTCTGATATTAT | 59349 |
rs534241242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894131 | CACCACCATTATATA[C/T]GTAAAGGTCTGACAG | 59349 |
rs534282758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898479 | TTCAAAAGCCAATAT[A/G]TTACTATGAGACATT | 59349 |
rs534409052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897476 | TGATCCGCCAGCCTC[A/G]ACCTCCCAAAGTGCT | 59349 |
rs534421814 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930381 | TCACACCAAAGGAAC[C/T]AGTTCAGACTTCTGA | 59349 |
rs534480488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925377 | ACTAGCCACTATCTA[G/T]TCCATGTAAAAGCTC | 59349 |
rs534497940 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927200 | AGCGCCGCCCAGACC[C/G]GGAGGCTCTGGAGGC | 59349 |
rs534589877 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896790 | GCTGGATTAGCTATG[A/T]TCTGGAGGCAGAGAC | 59349 |
rs534645188 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900310 | GCACTTTGGGAGGCC[A/G]AAGTGGGCAGATTCC | 59349 |
rs534749641 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904878 | AATTTCCATTATATC[G/T]TCTTTGAGACAGTAA | 59349 |
rs534835300 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926476 | AAGACCCATTTTACA[C/G]AAAAGCGGGTGATTC | 59349 |
rs534996243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924698 | GTGTTTTACTACATA[G/T]TACACTATTCTAAGC | 59349 |
rs535050785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925387 | ATCTAGTCCATGTAA[A/G]AGCTCTCTCTTCTTC | 59349 |
rs535156574 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926409 | TCTACTTCTGTTTGT[A/T]GTTGGCATTTTACTC | 59349 |
rs535238777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918595 | AGCAAGACCTTTACA[C/T]CTGTCTCTGCTTAAT | 59349 |
rs535274522 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921881 | AATAACCAAAAAGCA[-/CT]CTCTACCAAAGCCAA | 59349 |
rs535383181 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918025 | ATAAAAATGCAAATA[A/C]ATTTGGTACAGGAGG | 59349 |
rs535453448 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929289 | TATTGGGGGCATTTT[G/T]GAAATATTCGTCGAT | 59349 |
rs535568080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893115 | ATCTAATAAAAAAAA[C/T]CAAGTTGCCACTGGA | 59349 |
rs535649226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914839 | CATTACACTCCAGCC[C/T]GGGCGACAAGAGCGA | 59349 |
rs535801669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906793 | CAGCCTCCAGAGTAG[C/T]TGGGATTACAGGTGT | 59349 |
rs535808501 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906263 | TCCGAGACCAGCCTG[A/G]CCAACGTGGTGAAAC | 59349 |
rs535812179 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906724 | TGGAGTACAATGGTG[C/T]AATCTTGGCTCACTG | 59349 |
rs536120107 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901460 | CAAACCCAGCTACCT[-/T]TTTTTTTTTTTTTTA | 59349 |
rs536209105 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922230 | TTCATCTGATTCTCA[A/C]AGCAACCTGGTAAGG | 59349 |
rs536598906 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891520 | GGGGCAGTAATCAGG[C/T]AGCTGAACTACTAGG | 59349 |
rs536600624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895114 | GAGTATTTGTCGGCT[A/G]GGCACAGTGGCTCAC | 59349 |
rs536657954 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202891041 | CAGCTTGAAGAGACA[A/G]GAGCTACGGCTGATC | 59349 |
rs536822205 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920752 | AGGTAGTTATCTATA[C/T]GCCAGGAATAAGTAA | 59349 |
rs536932849 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922323 | CTGTAATCCCAGCAC[G/T]TTGGGAGGCCGAGGT | 59349 |
rs537004331 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896364 | CTAATTTTTTTGTTT[A/T]CTTTTTTGTAGAGAC | 59349 |
rs537027814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926128 | AAAAAAAAAAAGAAA[C/G]TTCAATTGAGGACCC | 59349 |
rs537180800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898607 | CCACTAGTTTACAGG[C/T]AATACATGGGAGAAG | 59349 |
rs537256615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927833 | GAAAATACAAAAAAA[A/T]TAGCCGGGCGTTGTG | 59349 |
rs537263927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920212 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT | 59349 |
rs537292919 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927209 | CAGACCCGGAGGCTC[C/T]GGAGGCTCTGGAGCC | 59349 |
rs537396415 | snp | C/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892247 | GCATGTGGTAAGTTA[C/G]AAATGACAGGAAAGT | 59349 |
rs537416799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914980 | TGCCCTCAGACTAGC[C/T]ATGAGCAGACAATCA | 59349 |
rs537458343 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919398 | AATGGCCAGATAGAT[-/A]AAAGAGTATCCATGT | 59349 |
rs537467532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925646 | TATGTATGCTTTCTA[A/T]CCTAGAAGTTGCACA | 59349 |
rs537498811 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929407 | AGATCAACAACAACA[A/T]TAAATGTCCATTAAT | 59349 |
rs537605342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905678 | TTGCACAACTATTTG[C/T]GCATCCCTAATTCAG | 59349 |
rs537778988 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911811 | TCTCCTCCCTGCCGT[C/T]ATGTCTAAGTCAGAG | 59349 |
rs537812710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907488 | TCGCCTGTTGTCCCA[C/G]CTACTCGGGAGTCTG | 59349 |
rs537814682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899858 | ATAATAATAAATAAA[A/T]AAATCAAAGCATAAG | 59349 |
rs537822662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922643 | AGGCGCCCGCCACCA[C/T]GCACGGCTAATTTTT | 59349 |
rs538004285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902170 | GGCACAGTGGCTAGC[A/G]CCTGTAATCCCAGCA | 59349 |
rs538041004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909315 | AAAATTTACTTGAAA[A/G]ATAGATAACATACTA | 59349 |
rs538063866 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928721 | ATTTATTTTGGTGCA[C/T]TTAGTGACTGAAAAG | 59349 |
rs538177397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900397 | AAAAAAATAATAAAA[A/C]AAAATAGCCAGGTGT | 59349 |
rs538241790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914112 | GTTAAGCAAGGGCCA[A/G]GTACAGAGAGCATTA | 59349 |
rs538345129 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904000 | TATCTATGTATCTAT[C/G]TATCTATCTATCTAT | 59349 |
rs538351962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911719 | GGAGCTTCTCTAACA[C/T]CACTATGTTGCAGTT | 59349 |
rs538391264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894025 | AATCTAGTTGTAAGT[A/G]TCAACTGTCTTTATC | 59349 |
rs538505185 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905122 | CTTCAGCATTTCCCT[C/T]CTAGAACTTCTGAAA | 59349 |
rs538567926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897361 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 59349 |
rs538761030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911396 | CCAGGAAAAGAATTA[C/T]AGTCAATTTGGGTTA | 59349 |
rs539245954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924609 | TACAAATAAATAAAT[A/G]AAATTAAAAACAAAA | 59349 |
rs539299735 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926002 | CCTAGCTACCAAGAA[A/G]GCTGAGGCCCGAGAA | 59349 |
rs539423049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927928 | CGGAGGTTGCTGAGC[C/G]GAGATCGCGCCATTG | 59349 |
rs539458463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919394 | CACTTAATGGCCAGA[C/T]AGATAAAGAGTATCC | 59349 |
rs539506248 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901016 | ATGCCGCTACACTCC[A/C]GCCTGGGTGACAAAG | 59349 |
rs539556429 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907599 | CAAGACTCTGTCTTA[-/A]AAAAAAAAAAAAAAG | 59349 |
rs539559106 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891713 | CTTCTAGTTTATCCC[C/T]AGTTATACTGAACTC | 59349 |
rs539591712 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904012 | TATCTATCTATCTAT[C/G]TATTTATCTATCTAT | 59349 |
rs539604264 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906179 | AAGTAATGGCCAGGC[A/G]CGGTGGCTCATGCCC | 59349 |
rs539627221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913822 | TTGTCCAATACACTA[C/G]CCATGCGTGGCTATT | 59349 |
rs539726206 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910038 | TCTATTAACCTGACC[C/T]AAGAAGTTCTTAGTC | 59349 |
rs539781970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912611 | AAGGGAGGAAACTTT[A/G]GAGGCAGAAGCTCTG | 59349 |
rs539790537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928470 | ATCTGATTGCAGCAA[G/T]TATGTTTTACCTTCC | 59349 |
rs539995754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899358 | AATTGAGTGATGGGT[A/G]TGGGGGATCATTATA | 59349 |
rs540000119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908002 | ACCTTAGCACGCATC[A/G]TGAGTCCTCAGTCAG | 59349 |
rs540024734 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930068 | GAGAATCGCTTGAAC[A/C]CAGGGAGCAGAGGTT | 59349 |
rs540163202 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905719 | TCCAAAATGCTTCAA[A/T]GAGCATTTCCTTTGA | 59349 |
rs540197420 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901542 | CCTGAACTCAAGCGA[A/T]GCTTCTGCTTCGGCC | 59349 |
rs540310504 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907901 | CAACATAGTGAGACC[A/T]CATTTCTATTAAAAA | 59349 |
rs540364043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899944 | AGTTGGGAGAAGCTA[A/G]GACCACAAGTTATTT | 59349 |
rs540364181 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892012 | TTGTGGGGCTCTCCC[C/T]TTTGTTTCCCTCTAG | 59349 |
rs540479250 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921112 | GCCTCCCAGGTTCAA[C/G]TGTTTCTCGTGCCTC | 59349 |
rs540531628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895279 | ATGCCTGTAGTCCCA[A/G]CTACTCAGGAAGCTG | 59349 |
rs540568211 | snp | A/G | 3.31389e-05 | 0.00407042 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894733 | TCCATCAAAGCCTCC[A/G]GAGACATAGATCATA | 59349 |
rs540616231 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911629 | AGTCAGCTCTTGAAA[C/T]AATTTTAAGTCATAA | 59349 |