SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2318 | snp | C/G | 0.360632 | 0.224189 | intron-variant | HERC1 | GRCh38.p7 | 15:63709677 | TGAAATGAAAATATA[C/G]AAAGGAGGATGGGTA | 8925 |
rs884495 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63728941 | aaagaGCAGGTTTTA[A/T]AAAAAAAAAAAAAGA | 8925 |
rs1039819 | snp | G/T | 0.29278 | 0.246313 | intron-variant | HERC1 | GRCh38.p7 | 15:63733274 | TAGTTTTTATAATTA[G/T]GTACTTCCTGAAGAT | 8925 |
rs1063416 | snp | C/T | 0 | 0 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63729323 | CATCTTCAGCTTTTG[C/T]TGCCTCATGCCACAG | 8925 |
rs1063417 | snp | C/T | 0 | 0 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63729291 | TATTTATTCACGTTC[C/T]GCAAATTTGCTCAAA | 8925 |
rs1063418 | snp | C/T | 0 | 0 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63729279 | TTCTGCAAATTTGCT[C/T]AAAGAAAGTCCTTGG | 8925 |
rs1063419 | snp | A/G | 0 | 0 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63727783 | GATTGTTAACTCCCT[A/G]CTGTTACTCCCTGTG | 8925 |
rs1063420 | snp | G/T | 0 | 0 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63727771 | CCTGCTGTTACTCCC[G/T]GTGTCAGTGGCTCGG | 8925 |
rs1063421 | snp | G/T | 3.31835e-05 | 0.00407316 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63727756 | TGTGTCAGTGGCTCG[G/T]CCTTTATTGAGTTAC | 8925 |
rs1063422 | snp | C/T | 0 | 0 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63727731 | AGTTACCTCCTCGAC[C/T]TGTTGCCACCTCTTG | 8925 |
rs1063423 | snp | C/G | 0 | 0 | missense | HERC1 | GRCh38.p7 | 15:63727729 | TTACCTCCTCGACTT[C/G]TTGCCACCTCTTGAT | 8925 |
rs1063424 | snp | A/C | 0 | 0 | missense | HERC1 | GRCh38.p7 | 15:63727685 | TCCTGCCAGCTGCTG[A/C]TCTTTTAGAAGACCA | 8925 |
rs1065250 | snp | A/G | 0.262435 | 0.249691 | intron-variant | HERC1 | GRCh38.p7 | 15:63741702 | tgtatacccacatgc[A/G]aaagaatgaagttgg | 8925 |
rs1131647 | snp | C/T | 0.203267 | 0.245593 | utr-variant-3-prime, downstream-variant-500B | HERC1, FBXL22 | GRCh38.p7 | 15:63608914 | AAAGAAATTAGATGT[C/T]TTTATTTTTCTGTGA | 8925 |
rs1140416 | snp | C/T | 3.31972e-05 | 0.004074 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63727828 | CATAGATGTGATATA[C/T]GTCTCAGCTGCTGGC | 8925 |
rs1140418 | snp | A/T | | | synonymous-codon | HERC1 | GRCh38.p7 | 15:63727816 | ATACGTCTCAGCTGC[A/T]GGCAGTATGCTCTGC | 8925 |
rs1140419 | snp | A/G | | | synonymous-codon | HERC1 | GRCh38.p7 | 15:63727669 | TCTTTTAGAAGACCA[A/G]GAGTTACAGTGGCCT | 8925 |
rs1140421 | snp | A/G | | | missense | HERC1 | GRCh38.p7 | 15:63630500 | TGGCATCAAATGGAG[A/G]TGTGTATGCCTGGGG | 8925 |
rs1140422 | snp | C/G | 0.235955 | 0.249605 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63626108 | TGACACAGTGCCCCC[C/G]CAGTATGGGGCGCTG | 8925 |
rs1142731 | snp | A/G | 0.262159 | 0.249704 | intron-variant | HERC1 | GRCh38.p7 | 15:63741514 | caagaccagcctaac[A/G]tggtgaaaccccgta | 8925 |
rs1396712 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | HERC1 | GRCh38.p7 | 15:63770043 | ATTGCTTCAATAACT[C/T]CACATTACATATGGG | 8925 |
rs1396713 | snp | C/T | 0.493925 | 0.054776 | intron-variant | HERC1 | GRCh38.p7 | 15:63805739 | ACTGCTTGAGGTCAG[C/T]AGTTCAAGACCACCC | 8925 |
rs1470314 | snp | C/T | 0.446641 | 0.154377 | intron-variant | HERC1 | GRCh38.p7 | 15:63820825 | CCAGCTTAACAGAGA[C/T]TTTAAATCAGGAGTT | 8925 |
rs1815128 | snp | C/T | 0.462472 | 0.13174 | intron-variant | HERC1 | GRCh38.p7 | 15:63643972 | GACAGACAGAACCAT[C/T]AGCCAACAAAAAGAG | 8925 |
rs1815129 | snp | C/G | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63639691 | TTGAGAGTGTCTACT[C/G]TAGAAACTGTGACAT | 8925 |
rs1815130 | snp | C/T | 0.462909 | 0.131034 | intron-variant | HERC1 | GRCh38.p7 | 15:63666563 | AATTTCCTAGTATTG[C/T]CCAAGTTTAATGAAA | 8925 |
rs1962180 | snp | A/G | 0.16618 | 0.23553 | intron-variant | HERC1 | GRCh38.p7 | 15:63690353 | ATTAAGTTATGGGGT[A/G]TGAGAAGTAGAGGGA | 8925 |
rs1986864 | snp | A/G | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63783806 | ggtgcagtggctcac[A/G]cctgtaatcccaaca | 8925 |
rs2053591 | snp | A/G | 0.46703 | 0.124089 | intron-variant | HERC1 | GRCh38.p7 | 15:63826458 | GTACAATGTGAACCA[A/G]TAACTACCATATCAC | 8925 |
rs2053592 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63826479 | ACCATATCACATATT[C/T]TAGCCTAAGAAATAT | 8925 |
rs2053593 | snp | A/G | 0.463018 | 0.130857 | intron-variant | HERC1 | GRCh38.p7 | 15:63826664 | ACATGTATGAATGCA[A/G]TATTAGTGGACAATG | 8925 |
rs2063281 | snp | A/G | 0.445196 | 0.1562 | intron-variant | HERC1 | GRCh38.p7 | 15:63769326 | catgaggctgaggca[A/G]ggagaactgcttgaa | 8925 |
rs2089619 | snp | C/G | 0.478768 | 0.100824 | intron-variant | HERC1 | GRCh38.p7 | 15:63744754 | tgggctacaggagaa[C/G]ccactgccctgaagg | 8925 |
rs2099920 | snp | A/G | 0.462691 | 0.131387 | intron-variant | HERC1 | GRCh38.p7 | 15:63811548 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 8925 |
rs2099921 | snp | A/T | 0.462909 | 0.131034 | intron-variant | HERC1 | GRCh38.p7 | 15:63811650 | ccgtctctcctaaaa[A/T]tatacaaaattagcc | 8925 |
rs2099922 | snp | C/T | 0.436834 | 0.166111 | intron-variant | HERC1 | GRCh38.p7 | 15:63812069 | CAGATTTGTAACTCT[C/T]GCTCAAAAATGAGCT | 8925 |
rs2165882 | snp | A/G | 0.366885 | 0.220993 | intron-variant | HERC1 | GRCh38.p7 | 15:63800591 | AAGGTATCCCTGACT[A/G]TACCCATGTGAGATT | 8925 |
rs2175087 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63766552 | tcattctgtcaccta[A/G]gctggagtgcagtgg | 8925 |
rs2175088 | snp | A/G | 0.460477 | 0.134905 | intron-variant | HERC1 | GRCh38.p7 | 15:63761494 | tgggaggctgaggct[A/G]gaagatcacttgagc | 8925 |
rs2197260 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | HERC1 | GRCh38.p7 | 15:63816635 | ATCCTTTAAATAAAG[C/T]GTATTTATTCAACAT | 8925 |
rs2202867 | snp | C/T | 0.475877 | 0.107142 | intron-variant | HERC1 | GRCh38.p7 | 15:63711963 | CTATCTAGAAGATTG[C/T]TTCTACTTGAGGAAC | 8925 |
rs2228509 | snp | C/T | 3.31268e-05 | 0.00406968 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63635991 | GCGGCCCAGGCAGAT[C/T]GAGGCCTTACAAGGA | 8925 |
rs2228510 | snp | A/G | 0.49486 | 0.0504326 | missense | HERC1 | GRCh38.p7 | 15:63678257 | GCCACTATTCAGCTC[A/G]TCCGTATCCTTCACC | 8925 |
rs2228511 | snp | A/G | 0.378409 | 0.214502 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63661830 | TGGGAGTGGAAATCC[A/G]TACTACCTGTTATGT | 8925 |
rs2228512 | snp | A/G/T | 0.0478626 | 0.147113 | missense | HERC1 | GRCh38.p7 | 15:63689654 | GATTGTATGTGGGAG[A/G/T]CACCCATTGCTCAGG | 8925 |
rs2228513 | snp | C/T | 0.0772275 | 0.180692 | missense | HERC1 | GRCh38.p7 | 15:63658688 | TAGAAAAGAGCTCCT[C/T]TGGGAGAATAACGTT | 8925 |
rs2228514 | snp | C/T | 0.00461136 | 0.0477955 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63775054 | TCTCAGTCTTTGCAA[C/T]GATGTCATTCATACT | 8925 |
rs2228515 | snp | A/G | 0.0431228 | 0.140363 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63774838 | ACGAGGCTCATTGCG[A/G]TATCTTCTTGAATGG | 8925 |
rs2228516 | snp | A/G | 0.00620554 | 0.0553558 | missense | HERC1 | GRCh38.p7 | 15:63626080 | CTGAGAGAAGTCAGC[A/G]TTCACACGGTGCGGG | 8925 |
rs2228517 | snp | C/G | 0.4903 | 0.0689643 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63640314 | CCACCAGAACTGTCT[C/G]CCTGACCCTGCATCC | 8925 |
rs2228518 | snp | C/T | 0.00594543 | 0.0541975 | synonymous-codon, downstream-variant-500B | HERC1, FBXL22 | GRCh38.p7 | 15:63609108 | GAGAAACGTGGACAA[C/T]GCCGAGGGCTCCGAC | 8925 |
rs2228519 | snp | C/T | 0.00382414 | 0.0435597 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63725295 | ATGGACACTCCTCAA[C/T]TGGGTAATGTGCTTC | 8925 |
rs2229748 | snp | C/T | 0.000827691 | 0.0203263 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63661959 | GTGTGAATGCAGCGT[C/T]GTCAGCTTCAATCAG | 8925 |
rs2229749 | snp | C/G | 0.377861 | 0.214851 | missense | HERC1 | GRCh38.p7 | 15:63645010 | AGAAGGATGGTGGGA[C/G]CAGGAATCAAATTGC | 8925 |
rs2255243 | snp | C/G | 0.375307 | 0.21634 | missense | HERC1 | GRCh38.p7 | 15:63696158 | TTGGACACACAGGAG[C/G]CAAGGGAGAGAGTGG | 8925 |
rs2271241 | snp | C/T | 0.499553 | 0.0149478 | intron-variant | HERC1 | GRCh38.p7 | 15:63756791 | ATACTTCTGTGAGTA[C/T]CAAAGTATAATATTT | 8925 |
rs2272209 | snp | C/T | 0.377072 | 0.215297 | intron-variant | HERC1 | GRCh38.p7 | 15:63660954 | GTTTGTTTTGAGAGC[C/T]TCTTTATTTTACATG | 8925 |
rs2414823 | snp | A/G | 0.463451 | 0.130149 | intron-variant | HERC1 | GRCh38.p7 | 15:63781554 | ttggtagagcagtca[A/G]aacacgtaccattta | 8925 |
rs2414824 | snp | A/G | 0.311369 | 0.242351 | intron-variant | HERC1 | GRCh38.p7 | 15:63703713 | ttattttgtagaaac[A/G]gggtttcgccatgtt | 8925 |
rs2414825 | snp | A/C | 0.462909 | 0.131034 | intron-variant | HERC1 | GRCh38.p7 | 15:63681284 | agcccaggaatttga[A/C]gcttcagtgagccat | 8925 |
rs2414826 | snp | C/T | 0.462144 | 0.132269 | intron-variant | HERC1 | GRCh38.p7 | 15:63679003 | TTTTAACATTTACAG[C/T]GTGACTGGCAATGTA | 8925 |
rs2414827 | snp | A/G | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63663872 | GATTCAGTAATTTAC[A/G]GGAACAGTGAGAGAA | 8925 |
rs2414828 | snp | G/T | 0.463018 | 0.130857 | intron-variant | HERC1 | GRCh38.p7 | 15:63663377 | GCTATTATTATCCCC[G/T]TTTGCAAGAGAGGAA | 8925 |
rs2899693 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | HERC1 | GRCh38.p7 | 15:63740966 | tcttagctatgacat[A/C]aaaagcacaaacaac | 8925 |
rs2899694 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HERC1 | GRCh38.p7 | 15:63703283 | TGTTGAACCACAATT[A/G]CGCCTTTTTCTCCCC | 8925 |
rs2899695 | snp | C/T | 0.205417 | 0.245993 | intron-variant | HERC1 | GRCh38.p7 | 15:63681169 | acaaaacaatacaCC[C/T]AGTCTCAGGCTTAAT | 8925 |
rs3056822 | in-del | -/CAAC | 0.416992 | 0.186048 | intron-variant | HERC1 | GRCh38.p7 | 15:63800886 | ggttgccagagaaac[-/CAAC]caagtgataaaagtg | 8925 |
rs3736570 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63637801 | TTATAGTCATCAAGG[A/T]GTTACGGGACTGCAT | 8925 |
rs3764186 | snp | A/G | 0.498685 | 0.0256094 | intron-variant | HERC1 | GRCh38.p7 | 15:63764238 | CTAATTTTAATGCAT[A/G]TGTCTCTCCCCTTCC | 8925 |
rs3764187 | snp | C/T | 0.00978769 | 0.0692679 | missense | HERC1 | GRCh38.p7 | 15:63718808 | AAACACACAAATTTA[C/T]TTAGTCAAGCATGTG | 8925 |
rs3830606 | in-del | -/GTTACGGGACTGCATAGTTATA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63637779 | TATAGTCATCAAGGA[-/GTTACGGGACTGCATAGTTATA]TCAACTCTTCCCTTT | 8925 |
rs4267257 | snp | A/G | 0.248188 | 0.249993 | intron-variant | HERC1 | GRCh38.p7 | 15:63805938 | ACAGAGCAAGACCCT[A/G]TCTCAAAACAAAAAA | 8925 |
rs4283174 | snp | A/G | 0.465368 | 0.126951 | intron-variant | HERC1 | GRCh38.p7 | 15:63613344 | TGGGGAGTGCCAAGT[A/G]GGGTGCAACCAGGGG | 8925 |
rs4332694 | snp | C/T | 0.00105656 | 0.02296 | intron-variant | HERC1 | GRCh38.p7 | 15:63669740 | TAAAAATCCAATTTA[C/T]GAAATAATACATACA | 8925 |
rs4344682 | snp | A/G | 0.471863 | 0.115225 | intron-variant | HERC1 | GRCh38.p7 | 15:63632111 | AACATAACTAAAACT[A/G]AATTCCTTACCCTTC | 8925 |
rs4411464 | snp | C/T | 0.464096 | 0.129085 | intron-variant | HERC1 | GRCh38.p7 | 15:63703224 | ACATATTCACTTTCT[C/T]AGACCAAGGGCTTAG | 8925 |
rs4412925 | snp | G/T | 0.17654 | 0.238964 | intron-variant | HERC1 | GRCh38.p7 | 15:63613411 | AATATTATACAGTAG[G/T]GCATACCCTACACAC | 8925 |
rs4523879 | snp | A/G | 0.463451 | 0.130149 | intron-variant | HERC1 | GRCh38.p7 | 15:63623180 | GTTCAAATCGAATCA[A/G]TAATGATAGCCAACC | 8925 |
rs4536410 | snp | C/T | 0.477684 | 0.103247 | intron-variant | HERC1 | GRCh38.p7 | 15:63773366 | GGAGAATCGCTTGAA[C/T]CCAGGAGGCAGAGGT | 8925 |
rs4577025 | snp | A/G | 0.439502 | 0.163061 | intron-variant | HERC1 | GRCh38.p7 | 15:63826856 | ataaagtatgacaac[A/G]tattctgttggtgct | 8925 |
rs4603505 | snp | C/T | 0.465578 | 0.126594 | intron-variant | HERC1 | GRCh38.p7 | 15:63623346 | ACTTTATTTTTCTAA[C/T]TCCCCTGGAATCTGG | 8925 |
rs4776363 | snp | A/G | 0.466618 | 0.124806 | intron-variant | HERC1 | GRCh38.p7 | 15:63829801 | GCCCCAGAATATAAG[A/G]AAGTGCTTGAAAAAG | 8925 |
rs4776681 | snp | A/T | 0.463774 | 0.129618 | intron-variant | HERC1 | GRCh38.p7 | 15:63807564 | GCTCTCCTTAACCCT[A/T]CCCAAAACTCTACAA | 8925 |
rs4776693 | snp | C/T | 0.463343 | 0.130326 | intron-variant | HERC1 | GRCh38.p7 | 15:63810313 | AAAATGTGGTGTATA[C/T]ACATACACTGAAATA | 8925 |
rs4776937 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829561 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 8925 |
rs4984252 | snp | A/G | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63609447 | TGCCCCGTGGCCCTC[A/G]AGGCTCTGGGTGAAG | 8925 |
rs4984253 | snp | A/C | 0.476227 | 0.106402 | intron-variant | HERC1 | GRCh38.p7 | 15:63627434 | CCCAGCACTTTGGGA[A/C]GCTGAGGCTTGAACT | 8925 |
rs4984304 | snp | C/G | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63622389 | CTGGAGTACAGTGGC[C/G]TGATCTCGGCTCACT | 8925 |
rs4984305 | snp | C/T | 0.441705 | 0.160466 | intron-variant | HERC1 | GRCh38.p7 | 15:63636812 | GTGGGAAAACTGAGT[C/T]ACAAAGAGGTCTCGA | 8925 |
rs4984306 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63646589 | ggcggatcatgaagt[C/T]aggaattcgagacca | 8925 |
rs4984307 | snp | C/T | 0.443464 | 0.15834 | intron-variant | HERC1 | GRCh38.p7 | 15:63657609 | ttcaaatcacttttg[C/T]taaacagaggttttc | 8925 |
rs4984310 | snp | C/T | 0.462363 | 0.131916 | intron-variant | HERC1 | GRCh38.p7 | 15:63667130 | tggccataagctcaa[C/T]gttagtgaataaaca | 8925 |
rs4984313 | snp | A/G | 0.477004 | 0.104734 | intron-variant | HERC1 | GRCh38.p7 | 15:63755579 | agctcaggagttcga[A/G]ttcagcctgggcaac | 8925 |
rs4984314 | snp | C/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63784618 | AAATTTTTTTTTTTT[C/T]CCTTTTTGAGACAGA | 8925 |
rs4984315 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | HERC1 | GRCh38.p7 | 15:63790597 | aaaaaTTTTTTTTTT[A/G/T]AAAAGTACTTTTTAA | 8925 |
rs4984317 | snp | C/T | 0.463989 | 0.129263 | intron-variant | HERC1 | GRCh38.p7 | 15:63792458 | AACCCTTTCCAGATA[C/T]AACCCTATCAGCAAA | 8925 |
rs4984318 | snp | C/T | 0.463989 | 0.129263 | intron-variant | HERC1 | GRCh38.p7 | 15:63792484 | GCAAAGCAGAATGAA[C/T]GTGTGCTTCCAGGAG | 8925 |
rs4984319 | snp | C/T | 0.463343 | 0.130326 | intron-variant | HERC1 | GRCh38.p7 | 15:63697105 | ttggtacaatactat[C/T]aactaaacctaaagt | 8925 |
rs6494418 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HERC1 | GRCh38.p7 | 15:63632138 | CTTCCCCACAAACCA[A/G]CTCATGTCCTCAGTC | 8925 |
rs6494419 | snp | G/T | 0.463343 | 0.130326 | intron-variant | HERC1 | GRCh38.p7 | 15:63651707 | CTAAACTCTTGGGAA[G/T]ACTTCAGAAAAGAAA | 8925 |
rs6494420 | snp | A/G | 0.140581 | 0.224783 | intron-variant | HERC1 | GRCh38.p7 | 15:63651743 | ACAGCTGGCTATAAA[A/G]CTATTAAAAATGCgg | 8925 |
rs6494423 | snp | C/T | 0.462909 | 0.131034 | intron-variant | HERC1 | GRCh38.p7 | 15:63668025 | gggttggtgctgcaa[C/T]ccctgcaatgttcaa | 8925 |
rs6494424 | snp | G/T | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63673240 | TTAATTGTTAAGGAA[G/T]CCTACAAATAAACAT | 8925 |
rs6494425 | snp | C/T | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63673506 | TTTTGTTAACTGCTG[C/T]CTCTCCAGAACCTAA | 8925 |
rs6494426 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HERC1 | GRCh38.p7 | 15:63682106 | taaatattgctgggg[A/G]aaaagaaagagacga | 8925 |
rs6494428 | snp | C/G | 0.463559 | 0.129972 | intron-variant | HERC1 | GRCh38.p7 | 15:63699526 | AACTTACACAAAAAG[C/G]AGACACAAACATCAC | 8925 |
rs6494429 | snp | C/T | 0.391111 | 0.206368 | intron-variant | HERC1 | GRCh38.p7 | 15:63718121 | acacacacacacaca[C/T]acaaccccctccttg | 8925 |
rs6494430 | snp | C/G | 0.305186 | 0.243833 | intron-variant | HERC1 | GRCh38.p7 | 15:63759925 | ATCTGAGGACAGCTG[C/G]CAGTCCCTAATAAAA | 8925 |
rs6494431 | snp | C/T | 0.322007 | 0.239405 | intron-variant | HERC1 | GRCh38.p7 | 15:63779266 | caatatacaaggtac[C/T]tgagaaaattaaccc | 8925 |
rs6494432 | snp | C/G | 0.308166 | 0.243139 | intron-variant | HERC1 | GRCh38.p7 | 15:63787598 | ATCAAGAATGACTTT[C/G]ATGGGTCAAACTATT | 8925 |
rs6494433 | snp | C/T | 0.464203 | 0.128908 | intron-variant | HERC1 | GRCh38.p7 | 15:63790711 | GTTATGTTTCCCTTT[C/T]TTTAAGTTTAAAAAT | 8925 |
rs6494434 | snp | C/G | 0.463018 | 0.130857 | intron-variant | HERC1 | GRCh38.p7 | 15:63793407 | attagtatgctaaaa[C/G]acactcccaacagtg | 8925 |
rs6494435 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | HERC1 | GRCh38.p7 | 15:63793524 | gcccacccctctccc[A/G]gaaaactcatgaata | 8925 |
rs6494436 | snp | C/T | 0.463343 | 0.130326 | intron-variant | HERC1 | GRCh38.p7 | 15:63799105 | AATCAGTCAATGACA[C/T]GGAGTTGTTCAACAA | 8925 |
rs6494437 | snp | A/G | 0.368324 | 0.220226 | intron-variant | HERC1 | GRCh38.p7 | 15:63799401 | GCTACTCAGGAGGCT[A/G]AGGTGGGAGGATCAC | 8925 |
rs6494438 | snp | C/T | 0.347473 | 0.230215 | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63834845 | ATATTCTAACGAGCA[C/T]CAATTAAACTGACCG | 8925 |
rs7162182 | snp | G/T | 0.172997 | 0.237846 | intron-variant | HERC1 | GRCh38.p7 | 15:63695926 | CGAGCCAGCAAATAA[G/T]CTACAATAGTACAAT | 8925 |
rs7162519 | snp | G/T | 0.0136876 | 0.081587 | missense | HERC1 | GRCh38.p7 | 15:63713477 | ACAGGGCACACCGAT[G/T]GATCACGGAGTTGCA | 8925 |
rs7162904 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63675377 | TGTATGCCAGGAGTT[A/G]GCAAACTTTCTGTAA | 8925 |
rs7163401 | snp | A/T | 0.464203 | 0.128908 | intron-variant | HERC1 | GRCh38.p7 | 15:63732592 | CTATTCTCATTCAGT[A/T]CCAAGTACATTGTTT | 8925 |
rs7163449 | snp | C/G | 0.307671 | 0.243257 | intron-variant | HERC1 | GRCh38.p7 | 15:63820976 | AAAAATTCAAGTTTT[C/G]TTTTCACATATTACT | 8925 |
rs7164301 | snp | C/T | 0.464416 | 0.128553 | intron-variant | HERC1 | GRCh38.p7 | 15:63742178 | aataatgttttgttc[C/T]ttcagtgtacaagtc | 8925 |
rs7164926 | snp | C/T | 0.461813 | 0.132798 | intron-variant | HERC1 | GRCh38.p7 | 15:63757480 | ccatgttggtcaagc[C/T]agtctcgaactcatg | 8925 |
rs7165167 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | HERC1 | GRCh38.p7 | 15:63824544 | atctcaaaaaaaaaa[A/C]aaaaattaaaaagaa | 8925 |
rs7165538 | snp | A/G | 0.305186 | 0.243833 | intron-variant | HERC1 | GRCh38.p7 | 15:63736685 | acaatctcggctcac[A/G]gcaacctccacctct | 8925 |
rs7165577 | snp | A/C | 0.465996 | 0.12588 | intron-variant | HERC1 | GRCh38.p7 | 15:63824804 | aacaaaacaaatgaa[A/C]ctggaggacactgtc | 8925 |
rs7166206 | snp | A/G | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63687961 | AGTGAGCAAAAGGGA[A/G]AGGTCAaggaactct | 8925 |
rs7166366 | snp | A/G | 0.462691 | 0.131387 | intron-variant | HERC1 | GRCh38.p7 | 15:63672369 | TGAGCTTGACTATAT[A/G]ATCTCTTAGTTTCTT | 8925 |
rs7167009 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HERC1 | GRCh38.p7 | 15:63760320 | GAAAACTAATCCTAC[A/G]TAGAAATAAGCAACA | 8925 |
rs7167066 | snp | C/T | 0.260504 | 0.249779 | intron-variant | HERC1 | GRCh38.p7 | 15:63759817 | TGAAATGGGAGAGGA[C/T]AGGGTCATCTTGGTC | 8925 |
rs7167130 | snp | G/T | 0.178465 | 0.239547 | intron-variant | HERC1 | GRCh38.p7 | 15:63627462 | actccagacttgagg[G/T]caggagttcaagacc | 8925 |
rs7168440 | snp | C/T | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63668596 | aatgatgagtaaaga[C/T]aaaccatcctaacaa | 8925 |
rs7168622 | snp | A/C | 0.286564 | 0.247312 | intron-variant | HERC1 | GRCh38.p7 | 15:63668675 | ggcaaaaaaatatca[A/C]caaggataaaggcat | 8925 |
rs7168823 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | HERC1 | GRCh38.p7 | 15:63763865 | TTTCAATTAAAGTTA[C/G]CAGCACATAATTCAA | 8925 |
rs7169217 | snp | C/T | 0.461481 | 0.133325 | intron-variant | HERC1 | GRCh38.p7 | 15:63739230 | ttagatggagactcg[C/T]tctgttgcccaggct | 8925 |
rs7169472 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | HERC1 | GRCh38.p7 | 15:63742572 | gggaaggttttcagt[A/C]tttctccattgaata | 8925 |
rs7169570 | snp | A/G | 0.462472 | 0.13174 | intron-variant | HERC1 | GRCh38.p7 | 15:63684934 | gaatcgcttgaaccc[A/G]ggaggcggaggttgc | 8925 |
rs7170198 | snp | C/T | 0.463343 | 0.130326 | intron-variant | HERC1 | GRCh38.p7 | 15:63633442 | CCTTTGTATTGTTTT[C/T]TTAAAAGGAGACGTG | 8925 |
rs7170334 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | HERC1 | GRCh38.p7 | 15:63655228 | gcatggtggcatgtg[C/T]ctgtaatcccagcta | 8925 |
rs7170373 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63811708 | cagctactcaggagg[C/T]tgaggcaggagaatg | 8925 |
rs7170477 | snp | A/G | 0.306182 | 0.243605 | intron-variant | HERC1 | GRCh38.p7 | 15:63811578 | actttcggcggccga[A/G]acgggcagatcacga | 8925 |
rs7170608 | snp | C/G/T | 0.0201678 | 0.0984315 | intron-variant | HERC1 | GRCh38.p7 | 15:63685292 | attcagactgaactg[C/G/T]gagcacagagtggaa | 8925 |
rs7170659 | snp | A/G | 0.305934 | 0.243663 | intron-variant | HERC1 | GRCh38.p7 | 15:63811706 | cccagctactcagga[A/G]gctgaggcaggagaa | 8925 |
rs7170689 | snp | C/T | 0.467946 | 0.122472 | intron-variant | HERC1 | GRCh38.p7 | 15:63831046 | TGCAATACATGCTCA[C/T]AACAATGTATTTCAT | 8925 |
rs7170887 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | HERC1 | GRCh38.p7 | 15:63764307 | GTTTATATAATTATG[C/T]GCACTGAAACCAAAT | 8925 |
rs7170979 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | HERC1 | GRCh38.p7 | 15:63742685 | atcatgaaagaatgt[C/T]gaattttgtcagatg | 8925 |
rs7171693 | snp | A/G | 0.464416 | 0.128553 | intron-variant | HERC1 | GRCh38.p7 | 15:63737830 | tcaaaaatttgaagc[A/G]cactgattttctaag | 8925 |
rs7172272 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HERC1 | GRCh38.p7 | 15:63769463 | TTTTAGAGAAAATAA[A/G]TTTTGAAAAATATAG | 8925 |
rs7172848 | snp | C/T | 0.464416 | 0.128553 | intron-variant | HERC1 | GRCh38.p7 | 15:63739555 | acaaatggagttata[C/T]aggccgagcgcggtg | 8925 |
rs7173231 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63738412 | gatgtttacttaata[C/G]tattaaaccaatact | 8925 |
rs7173384 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63739660 | cctggccaacatggt[A/G]aaaccctgtctctac | 8925 |
rs7173437 | snp | A/G | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63808593 | ACACTGCTCATCAAT[A/G]TACTTTTTAACGAAA | 8925 |
rs7173984 | snp | C/T | 0.460027 | 0.135605 | intron-variant | HERC1 | GRCh38.p7 | 15:63778682 | TGACTGAAGAGAATG[C/T]AATTAAATTAAGAAT | 8925 |
rs7174139 | snp | C/T | 0.311614 | 0.242289 | intron-variant | HERC1 | GRCh38.p7 | 15:63731088 | ATGTTTTACACATTT[C/T]CATAAACCATGTGTA | 8925 |
rs7174224 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HERC1 | GRCh38.p7 | 15:63699490 | AAACATTACCAAAAA[A/T]TGAATATAGAAGGGC | 8925 |
rs7175463 | snp | A/G | 0.173643 | 0.238054 | intron-variant | HERC1 | GRCh38.p7 | 15:63669822 | TTATAGTTTAATGGA[A/G]GGTGGGGAGAAAGAC | 8925 |
rs7175527 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | HERC1 | GRCh38.p7 | 15:63670053 | AGTTACAGTGCAAAG[A/G]AGGCTTTTAAAGATA | 8925 |
rs7175717 | snp | C/T | 0.478932 | 0.10045 | intron-variant | HERC1 | GRCh38.p7 | 15:63748788 | CTATAAATTAGCCCA[C/T]GTGTATCTGAAAATA | 8925 |
rs7175726 | snp | A/C | 0.463451 | 0.130149 | intron-variant | HERC1 | GRCh38.p7 | 15:63765136 | ataggtaactactct[A/C]tgttcaccttatctt | 8925 |
rs7175789 | snp | C/T | 0.14933 | 0.228835 | intron-variant | HERC1 | GRCh38.p7 | 15:63630894 | TCTAAACTCGGTAAC[C/T]TGTTTCAAAATAAGA | 8925 |
rs7175855 | snp | C/G | 0.462582 | 0.131564 | intron-variant | HERC1 | GRCh38.p7 | 15:63639924 | CTATGTCATTGAGAG[C/G]TGGCAGGTTTACAAG | 8925 |
rs7176089 | snp | A/T | 0.230603 | 0.249246 | intron-variant | HERC1 | GRCh38.p7 | 15:63668335 | tgtctctacaaaaaa[A/T]tacagaaattagctg | 8925 |
rs7176100 | snp | A/G | 0.464309 | 0.12873 | intron-variant | HERC1 | GRCh38.p7 | 15:63715897 | TTAGAAGTTCCACAC[A/G]TGGAAAACATTATGG | 8925 |
rs7176133 | snp | C/T | 0.396846 | 0.202327 | intron-variant | HERC1 | GRCh38.p7 | 15:63718905 | GTCCCAATCTGAAAA[C/T]AAAAATGATGCATTG | 8925 |
rs7176437 | snp | C/T | 0.313082 | 0.241911 | intron-variant | HERC1 | GRCh38.p7 | 15:63726315 | TTGTACATTTGTTTT[C/T]AAAAGTTCTTGACTT | 8925 |
rs7176625 | snp | A/G | 0.310386 | 0.242597 | intron-variant | HERC1 | GRCh38.p7 | 15:63716142 | AGTACTAGCACAGTT[A/G]TAGGAGCCCCTGTCA | 8925 |
rs7176963 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | HERC1 | GRCh38.p7 | 15:63823405 | catcagccctatgac[A/G]tagcaactataatta | 8925 |
rs7177004 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63744166 | tgtgtgtgtgtgtgt[C/G]tctctctctctctct | 8925 |
rs7177295 | snp | A/G | 0.310878 | 0.242475 | intron-variant | HERC1 | GRCh38.p7 | 15:63709302 | GGCATGAGCCACTGC[A/G]CCTGGCCCAATCTTT | 8925 |
rs7177897 | snp | A/G | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63673750 | TGTTTTTTGAGACAG[A/G]GTCTCGCTCAGCCGC | 8925 |
rs7177972 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | HERC1 | GRCh38.p7 | 15:63665286 | tgcctgtaatcccag[C/G]actttggaagaccaa | 8925 |
rs7178104 | snp | C/T | 0.463018 | 0.130857 | intron-variant | HERC1 | GRCh38.p7 | 15:63813384 | CTAAAAGAGCCCATA[C/T]ATAGATTACTCCAAA | 8925 |
rs7178111 | snp | C/T | 0.469346 | 0.119947 | intron-variant | HERC1 | GRCh38.p7 | 15:63783312 | cagcaacccccatcc[C/T]gatcagtcagcagcc | 8925 |
rs7178288 | snp | A/G | 0.462909 | 0.131034 | intron-variant | HERC1 | GRCh38.p7 | 15:63673972 | TCAAGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 8925 |
rs7178853 | snp | C/T | 0.214468 | 0.247474 | intron-variant | HERC1 | GRCh38.p7 | 15:63615741 | ACCCAAGCATTCATG[C/T]GTACCTCCCGAGATG | 8925 |
rs7179735 | snp | A/C | 0.0693013 | 0.172766 | intron-variant | HERC1 | GRCh38.p7 | 15:63740838 | agaacctcatcagat[A/C]tatgacttacaagta | 8925 |
rs7180358 | snp | A/G | 0.441295 | 0.160954 | intron-variant | HERC1 | GRCh38.p7 | 15:63653216 | GAGGCCAAGGCAGGC[A/G]GATCACCTGAGGTCA | 8925 |
rs7181135 | snp | C/G | 0.17332 | 0.23795 | intron-variant | HERC1 | GRCh38.p7 | 15:63670511 | TTTCCTCTACTAAAT[C/G]ATGTTCGCCCAGTAA | 8925 |
rs7181265 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63740977 | ttttgatgtcatagc[C/T]aagaaaccattgcct | 8925 |
rs7182158 | snp | A/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63631938 | TCTCTCTCTCTGGGT[A/T]TTTTAGATGATACGA | 8925 |
rs7182375 | snp | A/G | 0.482979 | 0.0906686 | intron-variant | HERC1 | GRCh38.p7 | 15:63813431 | CTTCTTAATGTTTAC[A/G]AAATCTGAGTTACTT | 8925 |
rs7182603 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HERC1 | GRCh38.p7 | 15:63824271 | gggcgcagttgctca[C/T]gcctataatcccagc | 8925 |
rs7182782 | snp | C/T | 0.00657888 | 0.056975 | missense | HERC1 | GRCh38.p7 | 15:63649923 | CTACTAATCCTTTTC[C/T]TCCTAAAAGGGAAAA | 8925 |
rs7402318 | snp | C/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63641943 | AGAATAAGGCATCTA[C/G]TATATTTCAAAAGTC | 8925 |
rs7403455 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | HERC1 | GRCh38.p7 | 15:63791947 | GATTTAATCAACTGC[C/T]TTCCAGTGTAATTCT | 8925 |
rs7497924 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63728934 | ggtaaagaaagaGCA[A/G]GTTTTAAAAAAAAAA | 8925 |
rs8023359 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HERC1 | GRCh38.p7 | 15:63833360 | CGGCCGGCGCCTGGG[A/G]ACACCGGGGTCGCGG | 8925 |
rs8023719 | snp | C/T | 0.17461 | 0.238362 | intron-variant | HERC1 | GRCh38.p7 | 15:63657402 | aagactcactgaggt[C/T]gaacatcttttcatg | 8925 |
rs8023851 | snp | A/T | 0.17138 | 0.237316 | intron-variant | HERC1 | GRCh38.p7 | 15:63617378 | attccatggtgtata[A/T]gtgccacattttctt | 8925 |
rs8024070 | snp | C/T | 0.462253 | 0.132093 | downstream-variant-500B, utr-variant-3-prime | HERC1, FBXL22 | GRCh38.p7 | 15:63608320 | CTGTCCAGAGAAGGA[C/T]GCGTGGTACTGAGAG | 8925 |
rs8024347 | snp | C/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63713895 | ACTAATCTGCCTTTA[C/T]AGAATTTTAATGTAA | 8925 |
rs8024373 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63713994 | ccacatcatctgggc[A/G]cttgttagaaatgca | 8925 |
rs8024382 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829468 | tgtgtgtgcacatat[A/G]tgtttatataaatat | 8925 |
rs8024392 | snp | A/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63829479 | atatatgtttatata[A/T]atatatatatatata | 8925 |
rs8024505 | snp | A/C/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63713955 | ATcagttattttcaa[A/C/T]gtacggtcccagacc | 8925 |
rs8024509 | snp | C/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63713959 | gttattttcaacgta[C/T]ggtcccagaccagca | 8925 |
rs8024793 | snp | A/G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829470 | tgtgtgcacatatat[A/G/T]tttatataaatatat | 8925 |
rs8025309 | snp | A/C | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63692901 | TTCCCAAATATCAgg[A/C]caggcgcaatggctc | 8925 |
rs8025503 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63713842 | acatttaaaatatac[G/T]aaaatactatatttt | 8925 |
rs8025632 | snp | A/C | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63693036 | aaacacaaaaattag[A/C]tgggtgtggtggcac | 8925 |
rs8026492 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63717700 | acacggtgaaacccc[A/G]tgtctactaaaaata | 8925 |
rs8026567 | snp | A/C/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63717482 | CATTTATAATTTTAC[A/C/G]ATCATGTTATCAAGA | 8925 |
rs8026694 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63717827 | cagtgagccaagatc[A/G]tgccactgcgctcca | 8925 |
rs8026795 | snp | C/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63717732 | aaaaaattagcaggg[C/T]gtggtggtgcatgcc | 8925 |
rs8026841 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63717886 | aaaataaaataaaaa[A/G]CAAGTAGTTTCAATC | 8925 |
rs8027001 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63717938 | CTCTAATCATCAGAA[A/G]GCCTATTTTCCTAAC | 8925 |
rs8027132 | snp | C/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63717953 | AGCCTATTTTCCTAA[C/T]ATTCAGCTAAAATGA | 8925 |
rs8027262 | snp | A/G | 0.463451 | 0.130149 | intron-variant | HERC1 | GRCh38.p7 | 15:63642020 | TTTAACTCTGGCTCT[A/G]TGGTTTATTCTACAC | 8925 |
rs8027336 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | HERC1 | GRCh38.p7 | 15:63796748 | caggtcatagataca[C/T]tgaaaggttttcaga | 8925 |
rs8027347 | snp | C/T | 0.307671 | 0.243257 | intron-variant | HERC1 | GRCh38.p7 | 15:63798659 | TTTAGGATTGTCACT[C/T]CCCTAACAGATAATG | 8925 |
rs8027701 | snp | A/C | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63798850 | GGTCAGTTTTTTATA[A/C]GCCCTAAGCATTTAG | 8925 |
rs8027993 | snp | C/T | 0.367297 | 0.220775 | intron-variant | HERC1 | GRCh38.p7 | 15:63696771 | AAGGTAGTACTGCTA[C/T]TGCTTTCTTTATTAA | 8925 |
rs8028038 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63833751 | AGcacacacgcgcgc[A/G]cgcacacacacacac | 8925 |
rs8028039 | snp | A/G | 0.331874 | 0.236213 | intron-variant | HERC1 | GRCh38.p7 | 15:63833753 | CACACACGCGCGCGC[A/G]CACACACACACACAC | 8925 |
rs8028257 | snp | C/T | 0.463018 | 0.130857 | intron-variant | HERC1 | GRCh38.p7 | 15:63642024 | ACTCTGGCTCTGTGG[C/T]TTATTCTACACAGGC | 8925 |
rs8029020 | snp | A/T | 0.0908922 | 0.192833 | intron-variant | HERC1 | GRCh38.p7 | 15:63730297 | tcacctctaaaaaaa[A/T]ttttttttttaatta | 8925 |
rs8029051 | snp | G/T | 0.162381 | 0.234161 | intron-variant | HERC1 | GRCh38.p7 | 15:63645458 | TATAAAAACTAAGAC[G/T]TATAGATGCAAATTG | 8925 |
rs8029813 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HERC1 | GRCh38.p7 | 15:63734004 | cccaccgctataaaa[A/G]taagaaaaaaaaatt | 8925 |
rs8030077 | snp | A/T | 0.172674 | 0.237741 | intron-variant | HERC1 | GRCh38.p7 | 15:63637033 | GCTTCAGAGTCATTA[A/T]GAGTTCAGTTAATGA | 8925 |
rs8030164 | snp | C/T | 0.0246568 | 0.108261 | intron-variant | HERC1 | GRCh38.p7 | 15:63764216 | AAACATTGCGGGACA[C/T]AGCGTAGGAAGGGGA | 8925 |
rs8031818 | snp | C/T | 0.463018 | 0.130857 | intron-variant | HERC1 | GRCh38.p7 | 15:63767586 | acctgtagtcccagc[C/T]actggggaggctggg | 8925 |
rs8032074 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | HERC1 | GRCh38.p7 | 15:63825446 | taaattgcttacata[C/G]agcaatcatttcact | 8925 |
rs8032305 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63702952 | ctactaaaaatacaa[A/G]aattagctgggctta | 8925 |
rs8032611 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | HERC1 | GRCh38.p7 | 15:63730727 | tgcttaaatacttag[C/T]ggcagccagccatct | 8925 |
rs8032617 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63730769 | tcaaatgatttagaG[A/G]GAGAGAACAaatttg | 8925 |
rs8032655 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | HERC1 | GRCh38.p7 | 15:63730821 | ctttgaatgattcct[A/G]taactcctctgtgag | 8925 |
rs8033676 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63643291 | AAAGAAGTTTCCTCA[C/G]TATTCAAGAGATTAC | 8925 |
rs8034053 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63799984 | AAAAAAATATTTTTA[A/G]TTAGCCAGATGTGGT | 8925 |
rs8034342 | snp | C/T | 0.462909 | 0.131034 | intron-variant | HERC1 | GRCh38.p7 | 15:63746671 | TAGAATACAATGTGA[C/T]GTAATGAGAACATAT | 8925 |
rs8034675 | snp | C/T | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63746851 | GTACAGTTGAATATA[C/T]TGTATAGCTAAAATC | 8925 |
rs8035286 | snp | A/C | 0.444444 | 0.157135 | intron-variant | HERC1 | GRCh38.p7 | 15:63646835 | acaaacaaacaaaaa[A/C]aaaaacaaaacaaaa | 8925 |
rs8035561 | snp | C/T | 0.44252 | 0.159487 | intron-variant | HERC1 | GRCh38.p7 | 15:63698061 | tgattgcagcaatta[C/T]ttctgtgaggttcta | 8925 |
rs8036037 | snp | A/T | 0.31721 | 0.240796 | intron-variant | HERC1 | GRCh38.p7 | 15:63786218 | agtatgctatgattg[A/T]gcctgagaatagcca | 8925 |
rs8036500 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | HERC1 | GRCh38.p7 | 15:63831781 | TCCAATCACCAACAC[A/G]TTCTCCAAAATTTCT | 8925 |
rs8036503 | snp | C/T | 0.311123 | 0.242413 | intron-variant | HERC1 | GRCh38.p7 | 15:63707060 | AAAAACTCACATTAA[C/T]TAACATTGCAGAGTA | 8925 |
rs8037046 | snp | C/T | 0.479095 | 0.100076 | intron-variant | HERC1 | GRCh38.p7 | 15:63708623 | GAGAATAACAGTAGA[C/T]AACACGTCATATAAT | 8925 |
rs8037083 | snp | C/T | 0.473818 | 0.111381 | intron-variant | HERC1 | GRCh38.p7 | 15:63774328 | atagtaaatgtttaa[C/T]ataaattGGGAAATA | 8925 |
rs8037694 | snp | A/C | 0.236144 | 0.249616 | intron-variant | HERC1 | GRCh38.p7 | 15:63673687 | GAGACtttaaaattt[A/C]ttttaaaatatCTCT | 8925 |
rs8039099 | snp | A/C | 0.36606 | 0.221428 | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63835779 | tgaccttgtgatccg[A/C]ccgccttggcctccc | 8925 |
rs8039113 | snp | C/G/T | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63731487 | ACATTCCTTATAACT[C/G/T]TGGGAAAAATTTTTG | 8925 |
rs8040381 | snp | C/T | 0.459914 | 0.13578 | intron-variant | HERC1 | GRCh38.p7 | 15:63779884 | CCAGTAGTGGTGGTG[C/T]GCGCCTGTAGTCCCA | 8925 |
rs8040480 | snp | C/T | 0.35809 | 0.225425 | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63835770 | tcgaactcctgacct[C/T]gtgatccgaccgcct | 8925 |
rs8040757 | snp | A/T | 0.438526 | 0.164189 | intron-variant | HERC1 | GRCh38.p7 | 15:63795855 | aactcagaacttttt[A/T]aaagaggcaaaggca | 8925 |
rs8041075 | snp | A/G | 0.367913 | 0.220446 | intron-variant | HERC1 | GRCh38.p7 | 15:63670848 | gatcacttgaggcca[A/G]gagttcaagacaagc | 8925 |
rs8041136 | snp | C/T | 0.436976 | 0.165952 | intron-variant | HERC1 | GRCh38.p7 | 15:63771150 | GCCAAGTTCACACCA[C/T]TGCACTCCAGCCTGG | 8925 |
rs8042418 | snp | A/G | 0.463774 | 0.129618 | intron-variant | HERC1 | GRCh38.p7 | 15:63832686 | TTGGAAAAGGGCCCA[A/G]TGAAAAAGATAGTGA | 8925 |
rs8042627 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC1 | GRCh38.p7 | 15:63805139 | atcagtatttatagc[A/G]tctttattcataata | 8925 |
rs8042937 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | HERC1 | GRCh38.p7 | 15:63745319 | gggaccagttcagca[C/T]taggactcgcctaag | 8925 |
rs9652430 | snp | A/T | 0.471863 | 0.115225 | intron-variant | HERC1 | GRCh38.p7 | 15:63822599 | tcaaaaaaaaaaaaa[A/T]ttttaaataataatt | 8925 |
rs9672514 | snp | A/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63790186 | tctcctggaactcag[A/T]acatactcaataaac | 8925 |
rs9672729 | snp | C/T | 0.304937 | 0.243889 | intron-variant | HERC1 | GRCh38.p7 | 15:63761191 | tactagagaatgacc[C/T]tcaaactatcaaaaa | 8925 |
rs9744110 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63619831 | tatttctgtgggatc[C/G]gtggtgatatcccct | 8925 |
rs9920746 | snp | C/T | 0.0134647 | 0.0809385 | intron-variant | HERC1 | GRCh38.p7 | 15:63727874 | AACATGGGACAATTG[C/T]TTCAAATGAACTTTA | 8925 |
rs9921018 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HERC1 | GRCh38.p7 | 15:63810319 | tggtgtatacacata[C/T]actgaaatagtactc | 8925 |
rs9972399 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | HERC1 | GRCh38.p7 | 15:63745537 | ctttctgctctaaca[A/G]gatagcattgagttc | 8925 |
rs9972404 | snp | A/G | 0.463774 | 0.129618 | intron-variant | HERC1 | GRCh38.p7 | 15:63650710 | ACTGATAACCAAATT[A/G]GCATAAGAAACTTAC | 8925 |
rs9972479 | snp | A/G | 0.437542 | 0.165312 | intron-variant | HERC1 | GRCh38.p7 | 15:63776771 | AGGAGTTTGAGACCC[A/G]CCTGGACAACACAGT | 8925 |
rs9972484 | snp | C/G | 0.461481 | 0.133325 | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63834839 | TTCCAGATATTCTAA[C/G]GAGCATCAATTAAAC | 8925 |
rs9972527 | snp | C/T | 0.478437 | 0.10157 | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63835332 | TAAAATGTGTATTTC[C/T]GGTAAATGATGTAAG | 8925 |
rs9972554 | snp | A/G | 0.439085 | 0.163545 | intron-variant | HERC1 | GRCh38.p7 | 15:63649207 | AAAATACAAAAATTA[A/G]CTGGGCGTGGTGGCG | 8925 |
rs9972561 | snp | A/T | 0.462691 | 0.131387 | intron-variant | HERC1 | GRCh38.p7 | 15:63648930 | CAACCAACAAAATCT[A/T]GTGAGATGCATTCAC | 8925 |
rs9972569 | snp | C/T | 0.460925 | 0.134204 | intron-variant | HERC1 | GRCh38.p7 | 15:63774314 | ATAGTACTTGGCATA[C/T]AGTAAATGTTTAACA | 8925 |
rs9972573 | snp | C/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63649321 | TCGCGCCACTGCACT[C/T]CAGCCTGGTGACAGA | 8925 |
rs10152174 | snp | A/G | 0.287172 | 0.247221 | intron-variant | HERC1 | GRCh38.p7 | 15:63665906 | AACAAAAGTACAGAA[A/G]CTGGAATTTCACCTT | 8925 |
rs10152404 | snp | C/T | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63672267 | TGGTCAGCACGACAG[C/T]TGATTAGACCTGGGA | 8925 |
rs10152416 | snp | C/G | 0.206336 | 0.246157 | intron-variant | HERC1 | GRCh38.p7 | 15:63672262 | CTTGCTGGTCAGCAC[C/G]ACAGCTGATTAGACC | 8925 |
rs10152419 | snp | A/G | 0.462363 | 0.131916 | intron-variant | HERC1 | GRCh38.p7 | 15:63776021 | CCAGCCTGGGTGACA[A/G]AGCGAGACTCCGTCT | 8925 |
rs10152453 | snp | A/C | 0.463989 | 0.129263 | intron-variant | HERC1 | GRCh38.p7 | 15:63806414 | ACCAACACAGATTTA[A/C]TCACTTCCTCCTCTA | 8925 |
rs10152515 | snp | A/C | 0.264084 | 0.249603 | intron-variant | HERC1 | GRCh38.p7 | 15:63778180 | AATCCAGGGTACATG[A/C]TTTCACCTCCATCCA | 8925 |
rs10152669 | snp | A/G | 0.446249 | 0.154875 | intron-variant | HERC1 | GRCh38.p7 | 15:63825618 | AATCAGTAAAATGAA[A/G]TATTATTTGAAGTTT | 8925 |
rs10152687 | snp | G/T | 0.445987 | 0.155207 | intron-variant | HERC1 | GRCh38.p7 | 15:63825790 | TTTTTTTGAGATGGA[G/T]TCTCGTTCTTGTCCC | 8925 |
rs10152714 | snp | A/T | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63825769 | AAAGAAAAATAATAA[A/T]TTTTTTTTTTTTGAG | 8925 |
rs10162809 | snp | G/T | 0.444666 | 0.15686 | intron-variant | HERC1 | GRCh38.p7 | 15:63798826 | AATGGTAACTCATAG[G/T]TATATTAAGGTCAGT | 8925 |
rs10163125 | snp | C/G | 0.438105 | 0.164671 | intron-variant | HERC1 | GRCh38.p7 | 15:63800671 | CACCTTGCATGGTTT[C/G]CAATTATATATAATT | 8925 |
rs10519213 | snp | C/G | 0.222035 | 0.248431 | intron-variant | HERC1 | GRCh38.p7 | 15:63700492 | AATTACTATACTGGT[C/G]TCAATTAAACCCTAG | 8925 |
rs10519220 | snp | C/T | 0.216349 | 0.247725 | intron-variant | HERC1 | GRCh38.p7 | 15:63754921 | CCTGTTTCATGCTCA[C/T]GTTGACTTGTTTTCA | 8925 |
rs10519223 | snp | A/G | 0.499956 | 0.00469082 | intron-variant | HERC1 | GRCh38.p7 | 15:63642950 | TTTGATATAACTACA[A/G]TATTACCTTTGATCT | 8925 |
rs10524877 | in-del | -/TATATATAT | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63826814 | AAAAAAAAAAAAAAA[-/TATATATAT]ATATATATATATATA | 8925 |
rs10527229 | in-del | -/AAAT/AAATAAAT | | | intron-variant | HERC1 | GRCh38.p7 | 15:63789801 | GCGAGCCCTGTCTCA[-/AAAT/AAATAAAT]AAATAAATAAATAAA | 8925 |
rs10534978 | in-del | -/AC | | | intron-variant | HERC1 | GRCh38.p7 | 15:63813312 | GATAATCAGAGATGG[-/AC]ACACACACACACACA | 8925 |
rs10546655 | in-del | -/AA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63696950 | AAAAAAAAAAAAAAA[-/AA]TTATTTTGAAATAAT | 8925 |
rs10649206 | in-del | -/CTA/CTAT | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63616255 | AGGAGCCTGCTCTAT[-/CTA/CTAT]TAGAAGCTGTTTAAA | 8925 |
rs10717064 | in-del | -/T | 0.46014 | 0.13543 | intron-variant | HERC1 | GRCh38.p7 | 15:63790622 | TTTTAAATACTAGAA[-/T]AATAGACACCCAAAC | 8925 |
rs10851731 | snp | A/T | 0.377012 | 0.215332 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63630553 | GGCTGGAGTAATCAT[A/T]GAAGATGTGGCAGTT | 8925 |
rs11071759 | snp | C/T | 0.4862 | 0.0819127 | intron-variant | HERC1 | GRCh38.p7 | 15:63630275 | TTTTAAACCATGGTA[C/T]AATACTTCTTTGGCC | 8925 |
rs11071760 | snp | G/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63647849 | GAAAAGGGAACTCAC[G/T]TGTACACACGGGCCT | 8925 |
rs11071762 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | HERC1 | GRCh38.p7 | 15:63695141 | CCCAGGCTCAAGTGA[G/T]CCTCCCATCTCAGCC | 8925 |
rs11071763 | snp | C/T | 0.463989 | 0.129263 | intron-variant | HERC1 | GRCh38.p7 | 15:63702833 | TTAGCTGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 8925 |
rs11071764 | snp | C/T | 0.443464 | 0.15834 | intron-variant | HERC1 | GRCh38.p7 | 15:63702938 | GTGAAACTCCGTCTC[C/T]ACTAAAAATACAAAA | 8925 |
rs11290825 | in-del | -/A | 0.464416 | 0.128553 | intron-variant | HERC1 | GRCh38.p7 | 15:63760111 | AACTACTGGGGGCAG[-/A]AAAAAAAATTGAACT | 8925 |
rs11294857 | in-del | -/A | 0.17332 | 0.23795 | intron-variant | HERC1 | GRCh38.p7 | 15:63695756 | AGACATAAAGATAAC[-/A]ATTTTTTTCTAAGTT | 8925 |
rs11295020 | in-del | -/T | 0.453939 | 0.144598 | intron-variant | HERC1 | GRCh38.p7 | 15:63648658 | TTCTCACAATCTATA[-/T]TTCTACTTGTTTCTT | 8925 |
rs11301389 | in-del | -/A | 0.499354 | 0.0179596 | intron-variant | HERC1 | GRCh38.p7 | 15:63761587 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 8925 |
rs11307698 | in-del | -/A | 0.130351 | 0.219509 | intron-variant | HERC1 | GRCh38.p7 | 15:63805948 | ACCCTATCTCAAAAC[-/A]AAAAAAAAAAAACAA | 8925 |
rs11314964 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63700730 | AAAAAAAAAAAAAAA[-/A]GCTTAATTTTCATTC | 8925 |
rs11321548 | in-del | -/C | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63720137 | AGACAGGGTCTCACT[-/C]CTGCTGTCCAGGCTG | 8925 |
rs11338494 | in-del | -/T | 0.499928 | 0.00598999 | intron-variant | HERC1 | GRCh38.p7 | 15:63784606 | GTATTATCATGCAAA[-/T]TTTTTTTTTTTTCCT | 8925 |
rs11344315 | in-del | -/T | 0.465473 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63738982 | TGAAAAGTCAGTTTA[-/T]TTTTTTTTTTTCAAA | 8925 |
rs11353871 | in-del | -/A | 0.498908 | 0.0233371 | intron-variant | HERC1 | GRCh38.p7 | 15:63748962 | GACAATTTTTTTTCC[-/A]AAAAAAAAAAAAAAT | 8925 |
rs11365904 | in-del | -/T | 0.463881 | 0.12944 | intron-variant | HERC1 | GRCh38.p7 | 15:63655529 | GATTATTATCTATGG[-/T]TAACTCAAATCATAA | 8925 |
rs11386985 | in-del | -/G | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63673628 | ATACAAGATAAAACA[-/G]GAGCTTTTCTTTTTT | 8925 |
rs11447637 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63780032 | AAAAAAAAAAAAAAA[-/A]GATTATTTTATTCAA | 8925 |
rs11629816 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63686697 | ATAAATAGAGCATGG[G/T]CCCTTCCCCATAAAG | 8925 |
rs11630290 | snp | C/T | 0.287867 | 0.247116 | intron-variant | HERC1 | GRCh38.p7 | 15:63623587 | CCTACGTATCACTAA[C/T]AGCATCACTTTATAT | 8925 |
rs11630696 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63830333 | ttcttgcaaaacatg[C/T]ttaacctcaatcaaa | 8925 |
rs11630720 | snp | C/T | 0.498592 | 0.0264935 | intron-variant | HERC1 | GRCh38.p7 | 15:63692573 | TAAGAGCAGCTACAG[C/T]GAAGAGACAAGTTTA | 8925 |
rs11631176 | snp | C/T | 0.462472 | 0.13174 | intron-variant | HERC1 | GRCh38.p7 | 15:63751306 | TACAGTAACATGCAG[C/T]ACAGGTTTGTAACCT | 8925 |
rs11631436 | snp | A/G | 0.496063 | 0.0441942 | intron-variant | HERC1 | GRCh38.p7 | 15:63747680 | CATGCACACACGCGC[A/G]CGCACACACACACAC | 8925 |
rs11631544 | snp | C/T | 0.21695 | 0.247806 | intron-variant | HERC1 | GRCh38.p7 | 15:63806358 | TATCTCAAAGGTGAC[C/T]TCTTCCATGAAGCTT | 8925 |
rs11631837 | snp | C/T | 0.475877 | 0.107142 | intron-variant | HERC1 | GRCh38.p7 | 15:63654809 | GGGAGACGGAGGTTG[C/T]GGTGAGCCGAGACTG | 8925 |
rs11632718 | snp | A/G | 0.473359 | 0.112298 | intron-variant | HERC1 | GRCh38.p7 | 15:63725599 | TCCTACCGTACTGCA[A/G]TAAGATACTGATGCA | 8925 |
rs11632919 | snp | C/T | 0.445855 | 0.155373 | intron-variant | HERC1 | GRCh38.p7 | 15:63786239 | agaatagccactaca[C/T]gccaggctagacaac | 8925 |
rs11633180 | snp | C/G | 0.439363 | 0.163222 | intron-variant | HERC1 | GRCh38.p7 | 15:63685881 | actgatacaggctgg[C/G]ttattgtatctagat | 8925 |
rs11633830 | snp | C/T | 0.47743 | 0.103805 | intron-variant | HERC1 | GRCh38.p7 | 15:63761950 | AAAAACACATGTATA[C/T]ACATCCTAGCTCTGT | 8925 |
rs11634435 | snp | C/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63757411 | gagattataggcacg[C/T]gccatcatgcccggc | 8925 |
rs11634705 | snp | C/T | 0.477345 | 0.103991 | intron-variant | HERC1 | GRCh38.p7 | 15:63767693 | ACAAGAGCGAGGCTC[C/T]GTCTCAAAAACAAAA | 8925 |
rs11635117 | snp | A/C | 0.464947 | 0.127663 | intron-variant | HERC1 | GRCh38.p7 | 15:63820533 | ACTTGAATTATATCA[A/C]ATAAAAGTGGCCATC | 8925 |
rs11635351 | snp | C/G | 0.435407 | 0.167703 | intron-variant | HERC1 | GRCh38.p7 | 15:63637901 | GAAAGAAAAAGGAAG[C/G]GGTGATGGGGAAACA | 8925 |
rs11635472 | snp | C/T | 0.479502 | 0.0991411 | intron-variant | HERC1 | GRCh38.p7 | 15:63683491 | gttcttataaaatca[C/T]atgtctaacacttac | 8925 |
rs11635593 | snp | A/C | 0.475789 | 0.107327 | intron-variant | HERC1 | GRCh38.p7 | 15:63720660 | TTTAAGAAATTCTTA[A/C]AGCCCACAGAGAATC | 8925 |
rs11636284 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | HERC1 | GRCh38.p7 | 15:63614410 | GGTTATCAATACATT[C/T]CTAGTCAGTTATTTA | 8925 |
rs11636351 | snp | C/T | 0.446249 | 0.154875 | intron-variant | HERC1 | GRCh38.p7 | 15:63825139 | cttggcaaaacccca[C/T]ctcctcaaaaataca | 8925 |
rs11636604 | snp | C/T | 0.460477 | 0.134905 | intron-variant | HERC1 | GRCh38.p7 | 15:63689819 | TGATTATACCAGTGT[C/T]CAACAGCTACTTTTA | 8925 |
rs11636758 | snp | C/T | 0.475702 | 0.107512 | intron-variant | HERC1 | GRCh38.p7 | 15:63699289 | AAGGCAGAAGCTGTT[C/T]TCAAAATGCTTAGCT | 8925 |
rs11636783 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63821978 | aaaagtaaagcaaga[A/G]agataggggatgtag | 8925 |
rs11636784 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63821980 | aagtaaagcaagaga[A/G]ataggggatgtaggg | 8925 |
rs11637688 | snp | A/G | 0.462691 | 0.131387 | intron-variant | HERC1 | GRCh38.p7 | 15:63747375 | TGAGGCAAGAGAATC[A/G]CTTGAACCTGGGAGG | 8925 |
rs11638191 | snp | A/C | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63700428 | TAAACACTAATGCCC[A/C]CAGAGAAAACAAACT | 8925 |
rs11639343 | snp | C/T | 0.47709 | 0.104548 | intron-variant | HERC1 | GRCh38.p7 | 15:63765688 | ggaagccccccacct[C/T]gagttatcccatcct | 8925 |
rs11639412 | snp | A/T | 0.465052 | 0.127485 | intron-variant | HERC1 | GRCh38.p7 | 15:63820435 | CGATGCTTCTAAATT[A/T]TATTAACATTGAAAT | 8925 |
rs11639437 | snp | G/T | 0.463559 | 0.129972 | intron-variant | HERC1 | GRCh38.p7 | 15:63765754 | ttgatatattatgtc[G/T]ccctaaaatgtataa | 8925 |
rs11852578 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HERC1 | GRCh38.p7 | 15:63656998 | tactaccatgaatga[C/T]tggtctttagggggc | 8925 |
rs11852931 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | HERC1 | GRCh38.p7 | 15:63772068 | TGGAGGTTGCAGTGA[A/G]CCAAGATCACGCCAC | 8925 |
rs11852958 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | HERC1 | GRCh38.p7 | 15:63705180 | ttttttgagacaggg[A/T]ctcactgttgtcaca | 8925 |
rs11853112 | snp | C/T | 0.00952359 | 0.0683454 | intron-variant | HERC1 | GRCh38.p7 | 15:63763452 | ctgcatcatgagtaa[C/T]ctatcagtaaaaccc | 8925 |
rs11854088 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63781636 | caacaatattgaaat[C/T]aggccaactaataac | 8925 |
rs11854292 | snp | A/C | 0.463559 | 0.129972 | intron-variant | HERC1 | GRCh38.p7 | 15:63785630 | aaaaaattagccagg[A/C]atggtggcgcatgat | 8925 |
rs11854607 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HERC1 | GRCh38.p7 | 15:63740182 | cccaaagtgtgcaga[C/T]tacaggtgtgggcca | 8925 |
rs11854824 | snp | A/T | 0.479744 | 0.0985793 | intron-variant | HERC1 | GRCh38.p7 | 15:63709165 | CTAATATATATATAT[A/T]TTTTTTATTTTTTTG | 8925 |
rs11855988 | snp | C/T | 0.459914 | 0.13578 | intron-variant | HERC1 | GRCh38.p7 | 15:63616985 | CCTGCTCCAGAATGC[C/T]TTGTTTTCTAAAATC | 8925 |
rs11856836 | snp | C/T | 0.464203 | 0.128908 | intron-variant | HERC1 | GRCh38.p7 | 15:63729897 | AGGCGTGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 8925 |
rs11857705 | snp | A/C | 0.232943 | 0.249417 | intron-variant | HERC1 | GRCh38.p7 | 15:63652045 | agtctcaaaaaagaa[A/C]aaaacaaaacaaaac | 8925 |
rs11857749 | snp | C/G | 0.0926964 | 0.194308 | intron-variant | HERC1 | GRCh38.p7 | 15:63739929 | tattttttttttttt[C/G]agacagagtctcact | 8925 |
rs11857787 | snp | A/G | 0.233527 | 0.249457 | intron-variant | HERC1 | GRCh38.p7 | 15:63652042 | ctcagtctcaaaaaa[A/G]aaaaaaacaaaacaa | 8925 |
rs11858925 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HERC1 | GRCh38.p7 | 15:63795763 | tttataatctcacgc[A/G]tccaccctactgctg | 8925 |
rs12050559 | snp | C/T | 0.206642 | 0.246211 | intron-variant | HERC1 | GRCh38.p7 | 15:63767249 | ctcaggcaatccacc[C/T]gtctcggcctcccaa | 8925 |
rs12102137 | snp | A/G | 0.45843 | 0.138046 | intron-variant | HERC1 | GRCh38.p7 | 15:63611936 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 8925 |
rs12102213 | snp | A/G | 0.458084 | 0.138567 | intron-variant | HERC1 | GRCh38.p7 | 15:63712639 | CATATATGCAATATA[A/G]TTATTTCTCTTAAAG | 8925 |
rs12148083 | snp | C/T | 0.265453 | 0.249522 | intron-variant | HERC1 | GRCh38.p7 | 15:63750430 | CTTTGGCAAGACAAA[C/T]AGGTGACTGACTGAC | 8925 |
rs12148246 | snp | C/T | 0.000106311 | 0.00729002 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63645572 | ATGGCAGAGTGAATG[C/T]AGACAGCACCAGCAT | 8925 |
rs12148370 | snp | A/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63809456 | AAAGCATATAAAGAT[A/T]CATAAGCAATTACAG | 8925 |
rs12148660 | snp | C/T | 0.462144 | 0.132269 | intron-variant | HERC1 | GRCh38.p7 | 15:63818322 | AGCACTCCGGCTCAC[C/T]GAGCTCCCAAACAGC | 8925 |
rs12148663 | snp | G/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63793796 | CTGGAAGTTCCCTGt[G/T]ttagagatgtgtgaa | 8925 |
rs12148666 | snp | A/G | 0.307176 | 0.243374 | intron-variant | HERC1 | GRCh38.p7 | 15:63793842 | cttgagtaggagctg[A/G]gtaaaatgaggctga | 8925 |
rs12148696 | snp | A/T | 0.32885 | 0.23724 | intron-variant | HERC1 | GRCh38.p7 | 15:63714724 | GGCTAATTTTTTGTA[A/T]CTTTAGTAGAGATGG | 8925 |
rs12324009 | snp | A/G | 0.233818 | 0.249476 | intron-variant | HERC1 | GRCh38.p7 | 15:63653637 | tagtatctgcataga[A/G]catatatatatcctc | 8925 |
rs12324419 | snp | C/T | 0.233818 | 0.249476 | intron-variant | HERC1 | GRCh38.p7 | 15:63653333 | ctgtaatcccagcta[C/T]gcgggaggctgaggc | 8925 |
rs12324588 | snp | C/G | 0.175576 | 0.238665 | intron-variant | HERC1 | GRCh38.p7 | 15:63650660 | GAATGTACAAATGTA[C/G]AAATGTCAAGCACTT | 8925 |
rs12324720 | snp | A/G | 0.168785 | 0.236441 | intron-variant | HERC1 | GRCh38.p7 | 15:63799941 | ccagcctgagcctgc[A/G]caacagtgtgagact | 8925 |
rs12372939 | snp | G/T | 0.479258 | 0.0997024 | intron-variant | HERC1 | GRCh38.p7 | 15:63704693 | TGTTGCACATTATAC[G/T]AAACATCACTTAATT | 8925 |
rs12439722 | snp | A/G | 0.435407 | 0.167703 | intron-variant | HERC1 | GRCh38.p7 | 15:63648917 | CACTTCCCCCAGACA[A/G]CCAACAAAATCTTGT | 8925 |
rs12440258 | snp | C/T | 0.00475057 | 0.0485048 | intron-variant | HERC1 | GRCh38.p7 | 15:63749626 | AGTTAATACTATTTC[C/T]TTAAAAACAAATGAC | 8925 |
rs12442400 | snp | G/T | 0.00938946 | 0.0678717 | intron-variant | HERC1 | GRCh38.p7 | 15:63682038 | gggactcatgacTTA[G/T]CAgtggcagcaatga | 8925 |
rs12442486 | snp | C/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63611498 | GAGATGCAGCCCTGC[C/T]TGCTCCACAAGGCAC | 8925 |
rs12442511 | snp | C/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63611626 | CAAACAAGGCCATGC[C/T]TCAGCACAGGAAGAG | 8925 |
rs12442834 | snp | G/T | 0.00481925 | 0.0488508 | intron-variant | HERC1 | GRCh38.p7 | 15:63779462 | aaaaactacaggaga[G/T]gcaaggaaaCATAAA | 8925 |
rs12591663 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | HERC1 | GRCh38.p7 | 15:63701505 | CAGACCATAAGGTCT[C/T]TGTGACAACTACACA | 8925 |
rs12591708 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63766851 | cccagctaattttgt[A/T]tttttagcagagaag | 8925 |
rs12591798 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63672210 | TCAAAAACTTAGGGG[A/G]AAAAATTATCATCAT | 8925 |
rs12708478 | snp | C/T | 0.461148 | 0.133852 | intron-variant | HERC1 | GRCh38.p7 | 15:63802980 | TTCGGGAGGCCAAGG[C/T]GGGAGGCTCACTTGA | 8925 |
rs12899462 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | HERC1 | GRCh38.p7 | 15:63680243 | CACATTAGAATTGAA[A/C]GCTTTTATGAGACAG | 8925 |
rs12900106 | snp | G/T | 0.463559 | 0.129972 | intron-variant | HERC1 | GRCh38.p7 | 15:63723711 | TAACAAAAAACCAAC[G/T]CGTTCAAAATGGAAT | 8925 |
rs12900621 | snp | C/T | 0.460252 | 0.135255 | intron-variant | HERC1 | GRCh38.p7 | 15:63657309 | ctatgtttcccaggc[C/T]ggtctcaaactcctg | 8925 |
rs12900944 | snp | C/T | 0.459347 | 0.136653 | intron-variant | HERC1 | GRCh38.p7 | 15:63723755 | AGAAACAAGGAACCA[C/T]TGAAAATGCGACTAG | 8925 |
rs12900985 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63771487 | ccaggctggagtgca[A/G]tggtgcgatctcagc | 8925 |
rs12901438 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63829563 | tgtgtgtgtgtgtgt[A/G]tatatatatatatat | 8925 |
rs12901439 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63829565 | tgtgtgtgtgtgtat[A/G]tatatatatatatat | 8925 |
rs12901709 | snp | A/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63654027 | GAGAGTGACACAAAG[A/T]GAGAGACCTAAACTT | 8925 |
rs12901823 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829549 | catatatgtatgtgt[A/G]tgtgtgtgtgtgtat | 8925 |
rs12902833 | snp | A/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63653982 | GGAACATCTTTGTAA[A/T]TGTGTGCATGTGTAT | 8925 |
rs12903006 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63654071 | AAGAGAAGAGACTAT[A/T]TCATCTTACATAACG | 8925 |
rs12903007 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63654072 | AGAGAAGAGACTATT[A/T]CATCTTACATAACGT | 8925 |
rs12903326 | snp | A/G | 0.459801 | 0.135955 | intron-variant | HERC1 | GRCh38.p7 | 15:63766747 | caatggcacgatctc[A/G]gctcactataacctc | 8925 |
rs12904304 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63833755 | CACACGCGCGCGCGC[A/G]CACACACACACACAC | 8925 |
rs12906986 | snp | C/T | 0.462909 | 0.131034 | intron-variant | HERC1 | GRCh38.p7 | 15:63675782 | ATAAAAAGCTTTTGC[C/T]GGTATAAAGTTTTGT | 8925 |
rs12911666 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63726026 | tcgttctgtcactca[A/G]gctggagtgcagtgg | 8925 |
rs12912296 | snp | A/G | 0.478188 | 0.10213 | intron-variant | HERC1 | GRCh38.p7 | 15:63757970 | GCCTCAGCCTCCCAA[A/G]GTGCTGGGATTACAG | 8925 |
rs12912298 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63773618 | gcatgatctctgctc[A/T]ctgcaacctccgtct | 8925 |
rs12912303 | snp | G/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63748711 | AATATTTTTAATTGG[G/T]TAGAGTATCATTTTA | 8925 |
rs12912446 | snp | A/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63773635 | tgcaacctccgtctc[A/C]tgggttcaagcaatt | 8925 |
rs12912718 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63773656 | tcaagcaattctcct[A/G]cctcagcctcccaag | 8925 |
rs12912999 | snp | A/G | 0.463018 | 0.130857 | intron-variant | HERC1 | GRCh38.p7 | 15:63758101 | TTTAAAAAATACTCA[A/G]TATTATTTAATGCAA | 8925 |
rs12913540 | snp | G/T | 0.446118 | 0.155041 | intron-variant | HERC1 | GRCh38.p7 | 15:63744015 | tgcagcctcatagag[G/T]taccaccttgatggt | 8925 |
rs12913624 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63773659 | agcaattctcctgcc[G/T]cagcctcccaagtag | 8925 |
rs12913738 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63744164 | tgtgtgtgtgtgtgt[C/G]tctctctctctctct | 8925 |
rs12915304 | snp | A/G | 0.276534 | 0.248588 | intron-variant | HERC1 | GRCh38.p7 | 15:63682818 | ttttgtggcaactac[A/G]tctggatgtatgatt | 8925 |
rs12915455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63827231 | ggaattcgagaccag[A/C]ctgggcaacatgaca | 8925 |
rs12916245 | snp | A/T | 0.494692 | 0.0512434 | intron-variant | HERC1 | GRCh38.p7 | 15:63786935 | ATttttttttttttt[A/T]ttttttgagacggag | 8925 |
rs12916912 | snp | C/T | 0.463018 | 0.130857 | intron-variant | HERC1 | GRCh38.p7 | 15:63683019 | tgcgtgcctccagtc[C/T]cacctattcgggagg | 8925 |
rs13379670 | snp | C/T | 0.172028 | 0.23753 | intron-variant | HERC1 | GRCh38.p7 | 15:63776085 | AGTAATTTCTTCAGA[C/T]GTACCTTTTCCATTC | 8925 |
rs13379688 | snp | C/T | 0.460252 | 0.135255 | intron-variant | HERC1 | GRCh38.p7 | 15:63778472 | aagcatttgttgaaa[C/T]gcagaggaaagaaaa | 8925 |
rs16947311 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HERC1 | GRCh38.p7 | 15:63641097 | ATTCAGTCTGATACC[C/T]GCATCCATCCCTATC | 8925 |
rs16947322 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63653976 | CTGCCAGGAACATCT[C/T]TGTAATTGTGTGCAT | 8925 |
rs16947343 | snp | C/T | 0.479984 | 0.0980171 | intron-variant | HERC1 | GRCh38.p7 | 15:63677353 | TTTACATTGAGGGGA[C/T]AGAAATATGTGGTTT | 8925 |
rs16947363 | snp | A/C | 0.0034076 | 0.0411362 | missense | HERC1 | GRCh38.p7 | 15:63698919 | CAAAGGAATAGGAGG[A/C]GTTGCATAACCAGTC | 8925 |
rs16947373 | snp | C/T | 0.463989 | 0.129263 | intron-variant | HERC1 | GRCh38.p7 | 15:63706116 | ATCATTGGATTTACA[C/T]TATCTAAAACTGCTG | 8925 |
rs16947378 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | HERC1 | GRCh38.p7 | 15:63707433 | GAAGGCTTACAAGAA[C/G]AATGGAAGTATATTT | 8925 |
rs16947382 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HERC1 | GRCh38.p7 | 15:63711365 | AGATAATGAGTCAGA[C/T]TGATCAGATTTAAAA | 8925 |
rs16947389 | snp | A/C | 0.0566069 | 0.158427 | intron-variant | HERC1 | GRCh38.p7 | 15:63713047 | TGTCTGAGCACAAAG[A/C]CCTTCTCAAAATAAT | 8925 |
rs16947395 | snp | C/G/T | 0.0712382 | 0.175123 | intron-variant | HERC1 | GRCh38.p7 | 15:63725124 | CCATATTGTGCTGCA[C/G/T]GATTTAACCATTTTT | 8925 |
rs16947404 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | HERC1 | GRCh38.p7 | 15:63731769 | ATTCAAAGTTAAGTT[A/G]CACAGTACACTCTGA | 8925 |
rs16947416 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63756980 | TATCTTTCCAGGTTA[C/T]TGTCCAGGTTATGAT | 8925 |
rs16947432 | snp | A/C | 0.0973687 | 0.197999 | intron-variant | HERC1 | GRCh38.p7 | 15:63770165 | CTTGCTCTCCCCACA[A/C]CTCAATCGCTTTGTG | 8925 |
rs16947442 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | HERC1 | GRCh38.p7 | 15:63792168 | AGACCAGTGCAATTC[A/C]ATAAATATTAGATGG | 8925 |
rs16947451 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HERC1 | GRCh38.p7 | 15:63797310 | GTATAGCTTCTTCTA[C/T]CATTCCTTACTGTTC | 8925 |
rs16947456 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | HERC1 | GRCh38.p7 | 15:63802818 | TCTGAAGCTTTTAGC[A/G]TTCTCTAGGTGAACA | 8925 |
rs16947463 | snp | C/G | 0.0941369 | 0.195465 | intron-variant | HERC1 | GRCh38.p7 | 15:63812184 | ACAAGTTTACTTAGG[C/G]TTGTGTTTTTACAAA | 8925 |
rs16947468 | snp | C/T | 0.462691 | 0.131387 | intron-variant | HERC1 | GRCh38.p7 | 15:63813051 | TCAACTTACAATCAA[C/T]GATATTGAGATACAT | 8925 |
rs17185673 | snp | A/G | 0.204803 | 0.245881 | intron-variant | HERC1 | GRCh38.p7 | 15:63642657 | AGATAGTTTAGTGCT[A/G]CTGTCAAAAATCATG | 8925 |
rs17185876 | snp | A/G | 0.233235 | 0.249437 | intron-variant | HERC1 | GRCh38.p7 | 15:63654004 | CATGTGTATGTGTAC[A/G]TGTGAAAGAGAGTGA | 8925 |
rs17186380 | snp | A/G | 0.107694 | 0.205546 | intron-variant | HERC1 | GRCh38.p7 | 15:63676271 | ATGAGAGGAAAGGTC[A/G]ACACTTGCATGTCAT | 8925 |
rs17186513 | snp | G/T | 0.175576 | 0.238665 | intron-variant | HERC1 | GRCh38.p7 | 15:63688747 | AAATGAAGAGATGGA[G/T]TCACAAGATATAAAT | 8925 |
rs17186555 | snp | C/T | 0.205723 | 0.246048 | intron-variant | HERC1 | GRCh38.p7 | 15:63689128 | TTGGCAGAGAATATA[C/T]GGAGATCCGGGAGAA | 8925 |
rs17186681 | snp | A/T | 0.207864 | 0.246424 | intron-variant | HERC1 | GRCh38.p7 | 15:63696566 | AATAGGAAAAGTAGT[A/T]GCTTTGGATGTAGGA | 8925 |
rs17186968 | snp | G/T | 0.362523 | 0.223246 | intron-variant | HERC1 | GRCh38.p7 | 15:63706664 | TTTCAAAGACAATCA[G/T]ATCTAAATACATCAG | 8925 |
rs17187253 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HERC1 | GRCh38.p7 | 15:63716163 | GCCCCTGTCAGCTAA[C/T]ACAAATTGAGATCAC | 8925 |
rs17187281 | snp | C/T | 0.286042 | 0.247388 | intron-variant | HERC1 | GRCh38.p7 | 15:63716961 | GAACAAACCAAAAAT[C/T]AGAAATCTGCTAAGG | 8925 |
rs17187564 | snp | A/G | 0.267364 | 0.249396 | intron-variant | HERC1 | GRCh38.p7 | 15:63731277 | ACAAGACAATATGAG[A/G]ACACTGTAGGGCCCT | 8925 |
rs17188807 | snp | A/C | 0.319376 | 0.240181 | intron-variant | HERC1 | GRCh38.p7 | 15:63819086 | ATTAAGCAGCTTTCC[A/C]ATCACTTACTTTAGA | 8925 |
rs17766325 | snp | G/T | 0.204189 | 0.245767 | intron-variant | HERC1 | GRCh38.p7 | 15:63634956 | AAGTAAATCTGCCAT[G/T]TTTGGTATTAATATA | 8925 |
rs17772465 | snp | A/G | 0.232067 | 0.249356 | intron-variant | HERC1 | GRCh38.p7 | 15:63675307 | ATGGGGAGATGTGAT[A/G]CTAAATGCAGAAGCA | 8925 |
rs17772987 | snp | C/G | 0.328382 | 0.237395 | intron-variant | HERC1 | GRCh38.p7 | 15:63706450 | AAATTTTGTAAATAA[C/G]CCCTTTCCATCATAA | 8925 |
rs17773126 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | HERC1 | GRCh38.p7 | 15:63711531 | ATGAAACGTAAAGAC[A/C]CTGTTCAACTTTCCT | 8925 |
rs17773244 | snp | C/T | 0.458775 | 0.137524 | intron-variant | HERC1 | GRCh38.p7 | 15:63715951 | GGCTCTCTTCCTCAC[C/T]GCTCAGACGTCTTCG | 8925 |
rs17773700 | snp | C/T | 0.17138 | 0.237316 | intron-variant | HERC1 | GRCh38.p7 | 15:63757565 | AGCCACCATACCAGG[C/T]CTTTATTTACTTTTA | 8925 |
rs17773778 | snp | G/T | 0.26326 | 0.249648 | intron-variant | HERC1 | GRCh38.p7 | 15:63768819 | TGATGCCCACAACAT[G/T]TAGAGCTGTTACATA | 8925 |
rs17774168 | snp | A/G | 0.366885 | 0.220993 | intron-variant | HERC1 | GRCh38.p7 | 15:63798299 | CTTAGTGAAAACCCC[A/G]AATGACTACTCAGTG | 8925 |
rs17774449 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | HERC1 | GRCh38.p7 | 15:63808242 | AATGATTCTGAATAA[C/T]GGCTGCTATCAAACT | 8925 |
rs17774473 | snp | G/T | 0.306679 | 0.24349 | intron-variant | HERC1 | GRCh38.p7 | 15:63810512 | CCAATGACAGTTAAC[G/T]CTGGGAAAAACTAGG | 8925 |
rs17774730 | snp | A/G | 0.35207 | 0.228214 | intron-variant | HERC1 | GRCh38.p7 | 15:63822164 | TGCCTGGCCCGGTCA[A/G]GGAATACGGATAGTT | 8925 |
rs17774754 | snp | C/T | 0.12932 | 0.218944 | upstream-variant-2KB, utr-variant-5-prime | HERC1 | GRCh38.p7 | 15:63833957 | GAAAGACGTAAGAGG[C/T]GGCGGCAGCAGCGGC | 8925 |
rs17774833 | snp | A/C | 0.0141837 | 0.08301 | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63835430 | CATACTCAAAAACAA[A/C]AAGCAAAAGCTCCTC | 8925 |
rs28406692 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63826500 | TAAGAAATATTCTTA[C/G]AATTTCAGTTATCCT | 8925 |
rs28407740 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63659011 | GCCCATGTATCACAT[C/G]TACTGATTATAAGTG | 8925 |
rs28438975 | snp | A/G | 0.460365 | 0.13508 | intron-variant | HERC1 | GRCh38.p7 | 15:63787444 | TTTCAGGCATGAGCC[A/G]CCACGGCTGACCAAT | 8925 |
rs28454572 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63826814 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 8925 |
rs28462014 | snp | C/G | | | missense | HERC1 | GRCh38.p7 | 15:63654132 | ACTCTGTTCTGATGA[C/G]CCTCCAATTTGATAA | 8925 |
rs28481336 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63827005 | GAAATCTACCTTGAA[A/G]ATACGGTTCTAACGA | 8925 |
rs28487909 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HERC1 | GRCh38.p7 | 15:63660650 | AAAAATCAATGCTCA[C/T]CTCTATTTATTTTTT | 8925 |
rs28491763 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63736965 | TTATTAGAAATTTGA[C/G]GAAAGCCTTTATTAT | 8925 |
rs28495969 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HERC1 | GRCh38.p7 | 15:63703444 | TTAAACTTCAGTAAA[C/T]AGGATATAATTAAAC | 8925 |
rs28496317 | snp | C/T | 0.460813 | 0.134379 | intron-variant | HERC1 | GRCh38.p7 | 15:63803563 | AAAGTGCTAGGATTA[C/T]AGGCGTGAGCCAACA | 8925 |
rs28510144 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63770391 | ATTTGAAATGTCTGT[G/T]CATCCCTCTTTCATT | 8925 |
rs28521407 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HERC1 | GRCh38.p7 | 15:63799651 | GACTAGGCTTTGAAA[A/G]CAAAGAAAAATATAG | 8925 |
rs28534762 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63783789 | AACTCATGATCGGGC[C/G]GGGTGCAGTGGCTCA | 8925 |
rs28549901 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC1 | GRCh38.p7 | 15:63772134 | TCTCAAAAAAAAAAA[A/G]GGAAAAAGGAAAAAT | 8925 |
rs28550152 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63610889 | GAGACAGAGGGAGGA[C/G]AGGCACTCCTAACTG | 8925 |
rs28563785 | snp | A/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63716956 | CCCCTGAACAAACCA[A/C]AAATTAGAAATCTGC | 8925 |
rs28564545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63765241 | GTGGATTCAGTAATG[C/T]GACCATACCCTCCTT | 8925 |
rs28578382 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63827102 | GGTTGAAGAGGTTAA[A/G]AAACATCTACACAGT | 8925 |
rs28623578 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63787534 | GGTATGTTACTGAAA[C/G]AAGAGAGAACCAATG | 8925 |
rs28628559 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63821296 | GCAGTGGCTCACACC[G/T]GTAATCCCAGAACTT | 8925 |
rs28629789 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HERC1 | GRCh38.p7 | 15:63635890 | TATTTTCTGTTACCT[A/G]ATTTTAAGAAACCTA | 8925 |
rs28629845 | snp | C/T | 0.306927 | 0.243432 | intron-variant | HERC1 | GRCh38.p7 | 15:63814108 | GTACAGTATTTTAAG[C/T]TATAAAACTATATGT | 8925 |
rs28649170 | snp | C/T | 0.317692 | 0.240661 | intron-variant | HERC1 | GRCh38.p7 | 15:63814119 | TAAGTTATAAAACTA[C/T]ATGTACAGAATTTGG | 8925 |
rs28663335 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63735692 | AAAAACAGTGTTGGA[C/G]TAAGATAAACTCCAT | 8925 |
rs28667106 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HERC1 | GRCh38.p7 | 15:63776293 | TCCAAAACTGAGCTC[C/G]TATTCTACCAGTACC | 8925 |
rs28692801 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HERC1 | GRCh38.p7 | 15:63795716 | CCAGCAGTTCTGCCA[C/T]GAGAGTACACCGAAC | 8925 |
rs28703264 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63700536 | GTAACACGGAGCTAA[C/T]ATTACAAAGTAACTA | 8925 |
rs28715037 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63702909 | AGGAGTTCAAGACCA[A/G]CCTGGCCAACATGGT | 8925 |
rs28731493 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63629035 | AGCTCACTGCAAGCT[C/T]TGCCTCCCTGGTTCA | 8925 |
rs28744440 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63787537 | ATGTTACTGAAAGAA[A/G]AGAGAACCAATGGTG | 8925 |
rs28750783 | snp | C/G | 0.463774 | 0.129618 | intron-variant | HERC1 | GRCh38.p7 | 15:63620664 | AAGGACTTGGTTTAT[C/G]AATCTGGGTGCTCCT | 8925 |
rs28866524 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63743250 | TTTTCTTTTTTTTTC[C/T]TTTTTTCTTTTTCTT | 8925 |
rs28893904 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63743249 | ATTTTCTTTTTTTTT[C/T]TTTTTTTCTTTTTCT | 8925 |
rs34027439 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63656393 | CTCAGATGGATAAAG[-/T]AAAATGGATTTCTTA | 8925 |
rs34050259 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63677127 | GTGAAAACCTGAAAC[-/T]TTTTGAGCACCAACA | 8925 |
rs34059646 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63809790 | CTTGTTTAGAATAGC[-/A]AAAAAAAAAAAAAAA | 8925 |
rs34069674 | in-del | -/AC/ACAC/ACACAC | | | intron-variant | HERC1 | GRCh38.p7 | 15:63718083 | GGCAGCTATTATGTG[-/AC/ACAC/ACACAC]ACACACACACACACA | 8925 |
rs34071725 | in-del | -/GG | | | intron-variant, downstream-variant-500B | HERC1, FBXL22 | GRCh38.p7 | 15:63609315 | ATCAGAGTGCCATAA[-/GG]GGGGGAGTGGGGCTG | 8925 |
rs34143602 | snp | A/G | 0.483708 | 0.088773 | intron-variant | HERC1 | GRCh38.p7 | 15:63647859 | CTCACGTGTACACAC[A/G]GGCCTAGAGTGTGGA | 8925 |
rs34149329 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63826053 | CAGGTGTGAGCCACC[-/C]ACGCCCGGCCAAATA | 8925 |
rs34164820 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63760435 | GCAGAGACACCATCC[-/A]AAAAAAAAAAAAAAA | 8925 |
rs34171304 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63622682 | TATTTACTCCTTAGG[-/G]TTACAATGAGGACTG | 8925 |
rs34174368 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63738778 | ATGGCTGTCAAAGAG[-/C]ACCCAAAGAATAAAA | 8925 |
rs34176171 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63715898 | AGAAGTTCCACACGT[-/G]GGAAAACATTATGGC | 8925 |
rs34206776 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63821631 | CCTGGAGGCCAAGGT[-/G]GGGAGGATCACCTGA | 8925 |
rs34211504 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63656424 | GGGACCATTTGCAGT[-/C]CCCACATAACATTCA | 8925 |
rs34212136 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63759485 | TAATAAGTATCATGC[-/T]TTTTAAATTTTTTGG | 8925 |
rs34224459 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63749822 | TACGTTACACATAAC[-/T]TTCCTGAGATGATTA | 8925 |
rs34244043 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63816524 | GAATATCAACATTGT[-/G]CCTCTTAAAAAGAAC | 8925 |
rs34306111 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63789989 | TAAAAGGAAAACCCC[-/A]AAAAGTCTGTCAGAA | 8925 |
rs34321094 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63772123 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAGGGAA | 8925 |
rs34323931 | in-del | -/A/AA | 0.434976 | 0.168179 | intron-variant | HERC1 | GRCh38.p7 | 15:63776037 | GCGAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 8925 |
rs34324807 | snp | A/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63734269 | TGAATCTGATAACTT[A/C]TACTTGGTTGAGCAA | 8925 |
rs34333861 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63755846 | AGAGAAGATATGAGC[-/T]TCAGTTTCTTATGGT | 8925 |
rs34340226 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63678585 | CTGTTATTTACATTT[-/C]CCTGTAACTCATGAA | 8925 |
rs34366173 | in-del | -/TT | 0.463774 | 0.129618 | intron-variant | HERC1 | GRCh38.p7 | 15:63706716 | TTATTTACTATGCTC[-/TT]TTTTTTTTTTTGAGA | 8925 |
rs34370342 | snp | C/T | 0.277778 | 0.248452 | intron-variant | HERC1 | GRCh38.p7 | 15:63829513 | ATACACACACACACA[C/T]ATATAAATAATATGT | 8925 |
rs34439815 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63771027 | AACCCCGTCTCTACT[-/A]AAAATACAAAAATTA | 8925 |
rs34447047 | in-del | -/TCTA | 0.463234 | 0.130503 | intron-variant | HERC1 | GRCh38.p7 | 15:63616250 | AGTGCAGGAGCCTGC[-/TCTA]TCTATTAGAAGCTGT | 8925 |
rs34454089 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63728749 | TAGAAGGCAAAATTC[-/G]GGAGGATCCTCAACA | 8925 |
rs34468041 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63651749 | GGCTATAAAACTATT[-/A]AAAATGCGGCTGGGC | 8925 |
rs34470541 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63707900 | TGCCACTGCACTCCA[G/T]CCCGGATGACAGAGC | 8925 |
rs34479262 | snp | A/G | 0.460702 | 0.134554 | intron-variant | HERC1 | GRCh38.p7 | 15:63790624 | TTAAATACTAGAATA[A/G]TAGACACCCAAACTC | 8925 |
rs34484871 | snp | A/C | 0.0311137 | 0.120786 | missense | HERC1 | GRCh38.p7 | 15:63690546 | AAATAAAAACCTGGG[A/C]CATTTGATCATCTTC | 8925 |
rs34493970 | in-del | -/TCTA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63616251 | GTGCAGGAGCCTGCT[-/TCTA]CTATTAGAAGCTGTT | 8925 |
rs34502156 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63709789 | AAAAATCCTAGATTT[-/G]CTAGTGGGTTTACTG | 8925 |
rs34509006 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63712005 | ATTTTACCAGTGACA[-/G]CTGTAGCATACCTTT | 8925 |
rs34509496 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63677050 | ACATTGTACTTAGCA[-/G]GGTGAGCATCCCAAA | 8925 |
rs34530699 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63753521 | ATGAAATTGAAAACT[-/G]GGACAAATCATTAAA | 8925 |
rs34561486 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63778886 | ACATATGATGATATG[-/A]AAAATCCTGAATCAA | 8925 |
rs34562625 | snp | C/G | 0.233235 | 0.249437 | intron-variant | HERC1 | GRCh38.p7 | 15:63651819 | GGGGCAGGCAGATCA[C/G]AAGGTCAGGAGTTTG | 8925 |
rs34592204 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63621902 | TCGTCTAATTTTTTT[-/T]CAAGGTTTTTAACTT | 8925 |
rs34597690 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63833348 | CCCCGCTAAAGGCGG[C/T]CGGCGCCTGGGGACA | 8925 |
rs34609979 | in-del | -/A | | | frameshift-variant | HERC1 | GRCh38.p7 | 15:63723199 | TACTAACAGCATAGT[-/A]CCTGCATGCTGATCC | 8925 |
rs34617832 | in-del | -/CG | 0.0926964 | 0.194308 | intron-variant | HERC1 | GRCh38.p7 | 15:63739878 | GGACTTACACAATAA[-/CG]GCCCTTTGTGTCTGG | 8925 |
rs34628022 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63707237 | TTCTTTTCAAAACTT[-/C]CCACTAGCCTTCGCT | 8925 |
rs34651964 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63630663 | AACAAAAACATGTGG[-/G]AAATGTTATGCACCA | 8925 |
rs34726252 | snp | A/G | 0.460365 | 0.13508 | intron-variant | HERC1 | GRCh38.p7 | 15:63670091 | TGCAGTTACTTTTAA[A/G]TATTAATATAAACTC | 8925 |
rs34772807 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63614392 | ATGGCTGGCGTGCAG[-/A]AAGGTTATCAATACA | 8925 |
rs34774319 | in-del | -/A/AA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63824533 | GTGAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 8925 |
rs34864960 | in-del | -/AA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63754173 | GCAAGACCCTATCTC[-/AA]AAAAAAAAAAAAACT | 8925 |
rs34912552 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63735541 | TAAAATTTAAAGTAT[-/A]AAAAAAAAAAAAAAG | 8925 |
rs34930457 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63651477 | CATATAGACTAGAGT[-/C]GTATAACTGATTCTT | 8925 |
rs34958368 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63647093 | AACCCTGTCTCTACT[-/A]AAAATATAAAAATTA | 8925 |
rs34983409 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63710787 | ATGCAGGCAATAGCA[-/T]TTCCAGTCCTAAGAA | 8925 |
rs34990018 | in-del | -/C | 0.466412 | 0.125164 | intron-variant | HERC1 | GRCh38.p7 | 15:63816096 | ACAGCCAAACCATAT[-/C]ACCTAACATTTCCCA | 8925 |
rs34999313 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63713260 | TCTATGTTAACATCA[-/G]GAACACTGTAACTTT | 8925 |
rs35004522 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63719179 | AGGTAAGTGCTATGA[-/G]GGGAAAATAAAGCAG | 8925 |
rs35039072 | in-del | -/T | 0.498323 | 0.0289051 | intron-variant | HERC1 | GRCh38.p7 | 15:63695384 | TGAGTCTGTATAATC[-/T]TTTTTTTTTTTTTTT | 8925 |
rs35041070 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63628398 | CCATCTCAAAAAAAA[-/A]CTTAGTTGCTGCTAA | 8925 |
rs35072118 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63625157 | CACACACAATAGCTA[-/T]GCCACTTTGTTACTG | 8925 |
rs35074987 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63821750 | GTGATACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8925 |
rs35078406 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63764449 | AGTGATTTATTCCAA[-/G]GGGACACAGGGCTCT | 8925 |
rs35097725 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63671374 | AAGCAGCTGTCTCTT[-/A]AAAAAAAAAAAAAGT | 8925 |
rs35098067 | snp | A/G | 0.0223546 | 0.103332 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63690639 | TTAAGTTACCAACCA[A/G]AGGGATACCTGGAGG | 8925 |
rs35122568 | snp | C/G/T | 0.00302806 | 0.0387926 | missense | HERC1 | GRCh38.p7 | 15:63666028 | TGCCTAGAACGGCTG[C/G/T]TCCAGGCCTAGAGTC | 8925 |
rs35163901 | snp | A/G | 0.00272266 | 0.0367956 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63758295 | ACAGGTTTCGGAGAC[A/G]ATGGGAGCATCACCA | 8925 |
rs35177986 | snp | C/T | 0.277778 | 0.248452 | intron-variant | HERC1 | GRCh38.p7 | 15:63829501 | ATATATATATATATA[C/T]ACACACACACATATA | 8925 |
rs35178055 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63610638 | TAATCCTTCCTGCAC[-/T]GTGGCTTCTCCAGCA | 8925 |
rs35186319 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63817646 | TTGAACCCAGGAGTT[-/G]GGAGGTTGCAGTCAG | 8925 |
rs35209627 | in-del | -/AC | | | intron-variant | HERC1 | GRCh38.p7 | 15:63802158 | GGTCCAGGTCTCCCC[-/AC]TCCTGCCACATGTAC | 8925 |
rs35213471 | in-del | -/AA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63706031 | CAAGACCCTGTCTCC[-/AA]AAAAAAAAAAAAAAA | 8925 |
rs35216087 | snp | A/G | 0.445987 | 0.155207 | intron-variant | HERC1 | GRCh38.p7 | 15:63824990 | GCAGTTATGTAGGAT[A/G]AATAAATCTAGAGAT | 8925 |
rs35225324 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63794462 | CCCTTCCCAGAGGTT[-/G]GGGGATGGGGCTGAA | 8925 |
rs35244420 | in-del | -/T | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63697451 | TGATGTTAATCTTGA[-/T]TTTTTTTTTTTTTTT | 8925 |
rs35258975 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HERC1 | GRCh38.p7 | 15:63734024 | AAAAAAAAATTAGCC[A/G]GGTGTGGTGGCACGT | 8925 |
rs35263200 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63702676 | TATGAAAATTAAATG[-/A]AGTTACTATAATATT | 8925 |
rs35287299 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B | HERC1, FBXL22 | GRCh38.p7 | 15:63608935 | AATTTCTTTGTTACA[-/T]TTTAGAGTAACTAAA | 8925 |
rs35330672 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63706993 | CCCTAAAAACCCACT[-/G]GAACATAGCTATAAG | 8925 |
rs35357119 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | HERC1 | GRCh38.p7 | 15:63646836 | CAAACAAACAAAAAC[-/A]AAAACAAAACAAAAC | 8925 |
rs35360755 | snp | C/T | 0.441568 | 0.160629 | intron-variant | HERC1 | GRCh38.p7 | 15:63729995 | CACGCCATTGCACTC[C/T]AGCCTGGGCGACAAG | 8925 |
rs35361023 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63819737 | TGACAATACTTGGAT[-/G]GGGGTTTTCTATCAG | 8925 |
rs35375772 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63614382 | GCCTGGCACCATGGC[-/T]TGGCGTGCAGAAGGT | 8925 |
rs35376168 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63671844 | CTAACCATTCTGCTT[-/C]CCCTTATTTCACTTA | 8925 |
rs35383492 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63784919 | CTGGCCTATCAGTGC[-/A]AAATTTTCAAAAAGC | 8925 |
rs35393136 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63782342 | TTACATTCTGAAAAA[-/C]CTAGGGCACCTAAGA | 8925 |
rs35433809 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63801862 | AAGGCTTTTACCTAT[-/C]CTCATATGCTAATGA | 8925 |
rs35436692 | in-del | -/A/AAAA | 0.00517822 | 0.0506191 | intron-variant | HERC1 | GRCh38.p7 | 15:63784064 | GGAAGACTCTATCTC[-/A/AAAA]AAAAAAAAAAAAAAA | 8925 |
rs35448846 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63664161 | TAAACATTAAACATG[-/C]CATCATCACTTCTTA | 8925 |
rs35453064 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63745752 | TTCTTATGAAGGTGG[-/T]TTTTTTCTGTGTAGA | 8925 |
rs35463732 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63795245 | ATTGTCTTAGTTACT[-/A]AAAGCTTGCCTTTTT | 8925 |
rs35471228 | snp | A/T | 0.0192879 | 0.0962909 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63774937 | AATAGTGACTCCTTT[A/T]AGAAATGTTGTTACT | 8925 |
rs35478772 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63824238 | GTATGTAGGTTTCTC[-/A]AAAAATTAAAAAGGG | 8925 |
rs35490295 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63622345 | TTTTTTTTTTTTTTT[-/T]GAGATGTGGTCTCGC | 8925 |
rs35494311 | snp | C/T | 0.106278 | 0.204558 | intron-variant | HERC1 | GRCh38.p7 | 15:63801003 | AATCAACCAAGCCTA[C/T]GTAATGCAGCTTCCA | 8925 |
rs35497392 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63713884 | ATTAGGAAATACTAA[-/T]TCTGCCTTTACAGAA | 8925 |
rs35572967 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63625153 | CACGCACACACAATA[-/T]GCTAGCCACTTTGTT | 8925 |
rs35580549 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63821555 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8925 |
rs35582194 | in-del | -/G | | | frameshift-variant | HERC1 | GRCh38.p7 | 15:63635999 | GGCCTCGATCTGCCT[-/G]GGGCCGCCGCTGCCT | 8925 |
rs35600526 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63797066 | TGGTTAGAGAGCTTA[G/T]AATTTTATTTTTAGT | 8925 |
rs35630917 | in-del | -/TG | 0.483418 | 0.0895317 | intron-variant | HERC1 | GRCh38.p7 | 15:63829525 | CATATATAAATAATA[-/TG]TGTGTGCACATATAT | 8925 |
rs35633141 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63649034 | CCCTTCCTCCATTAC[-/T]TTCAATTTTACTCAT | 8925 |
rs35656049 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63795090 | AAAAAAAAAAAAAGT[A/G]AAGGAATAATCATCC | 8925 |
rs35671294 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63635829 | TGAATCTGAACATCC[-/A]AAACCAATGGATCTC | 8925 |
rs35693299 | in-del | -/TG/TGTG | 0.480384 | 0.177725 | intron-variant | HERC1 | GRCh38.p7 | 15:63829444 | AAAGAAACGTCAGTA[-/TG/TGTG]TGTGTGTGTGTGTGT | 8925 |
rs35700740 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63701023 | TTGAACTTGTTTTTT[-/G]GGGGGGGTGTTTTTT | 8925 |
rs35700814 | in-del | -/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63628954 | CAATAAAACACATTC[-/T]TTTTTTTTTTTTTTG | 8925 |
rs35704832 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63737604 | AGCTGGTCTTCAATT[-/C]CCTGGCCTCAGGTGG | 8925 |
rs35712767 | snp | A/T | 0.464096 | 0.129085 | intron-variant | HERC1 | GRCh38.p7 | 15:63786711 | AGGATGGCCAAATGC[A/T]TAGAGATAGAAAGTA | 8925 |
rs35714507 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63754009 | CAAAATCCTGTCTCT[-/A]AAAAAAATACAAAAC | 8925 |
rs35740360 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63786351 | TGCTGGTGGTATCTC[-/A]AAAAGTTAAAAACAG | 8925 |
rs35746319 | in-del | -/G | | | frameshift-variant | HERC1 | GRCh38.p7 | 15:63694375 | AAGCTGTGCTAAGCT[-/G]GGGAAACACCCGTCT | 8925 |
rs35775749 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63712420 | CCAAGTTTCTTGCTT[-/G]GGATAGTTAATGTAC | 8925 |
rs35798422 | in-del | -/A | 0.097727 | 0.198275 | intron-variant | HERC1 | GRCh38.p7 | 15:63828050 | AGATAGTTGTGATGG[-/A]TTGCACCATCTTGTG | 8925 |
rs35881317 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63730159 | TTTGTTTTTTCCATT[-/A]AAAAAAAAAAAGCAG | 8925 |
rs35900132 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63705407 | AGGTGTGAGCCACCA[-/C]CACCTGGCCCATTCT | 8925 |
rs35903771 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63817687 | CCACTACACTCCAGT[-/G]GTGGGTGACACAGCG | 8925 |
rs35918222 | snp | C/T | 0.00739679 | 0.0603629 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63666005 | GGGATCATTTGACTT[C/T]CCGCCACTGCCTAGA | 8925 |
rs35930148 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC1 | GRCh38.p7 | 15:63718292 | TGGCCCAATCAGCAC[A/G]AAGAGAGGAATAATC | 8925 |
rs35931984 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63610643 | CTTCCTGCACGTGGC[-/G]TTCTCCAGCAAGCCT | 8925 |
rs35943131 | snp | C/G | 0.460252 | 0.135255 | intron-variant | HERC1 | GRCh38.p7 | 15:63786454 | AAACTTGTACACAAA[C/G]ATTCACTGGAGCATT | 8925 |
rs35972003 | in-del | -/A | 0.461592 | 0.133149 | intron-variant | HERC1 | GRCh38.p7 | 15:63756269 | TAAGAATTAAAATTC[-/A]ATAATGTATACAAAG | 8925 |
rs35978932 | snp | C/T | 0.0330772 | 0.124276 | missense | HERC1 | GRCh38.p7 | 15:63733024 | GGTTGATCTGACAGA[C/T]TTCCGTAGCCAGTAC | 8925 |
rs35987092 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63663420 | TGGGTTATTGATAGG[-/T]TTTAAGTAAGAGAAT | 8925 |
rs36023704 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63696049 | TGAATCATAAACACC[-/A]AAAAGTTTCACATTA | 8925 |
rs36033932 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63661321 | ATAGTTGACAATTAA[-/G]GGGCAACAAACCTAC | 8925 |
rs36062023 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63649495 | ACAAAAGATGAATTA[-/T]CTAATGTTATAATAC | 8925 |
rs36068001 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63799442 | AGGTCAAGGCTGCCG[-/T]TGAGCTATGATCGTG | 8925 |
rs36070454 | in-del | -/T | 0.0926964 | 0.194308 | intron-variant | HERC1 | GRCh38.p7 | 15:63739877 | TGGACTTACACAATA[-/T]AGCCCTTTGTGTCTG | 8925 |
rs36081978 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63687880 | ATAGCCAGTTTAAAG[-/C]CCTAAGGAATGAGCA | 8925 |
rs36089909 | snp | A/C | 0.00317321 | 0.0397056 | missense | HERC1 | GRCh38.p7 | 15:63713584 | TCATCAGCTCGAGCC[A/C]CAGACCCTGCCCCAC | 8925 |
rs36111484 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829588 | TATATATATATATAT[-/A]ATATATAATATACTG | 8925 |
rs36115945 | in-del | -/G | 0.463343 | 0.130326 | intron-variant | HERC1 | GRCh38.p7 | 15:63695025 | ATTTACTATATTTCA[-/G]TATATAAAGTATATA | 8925 |
rs55640532 | snp | C/G | 0.444267 | 0.157354 | intron-variant | HERC1 | GRCh38.p7 | 15:63617731 | TGGTATTTCATTGTG[C/G]TTTTGATTTGCATTT | 8925 |
rs55678738 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | HERC1 | GRCh38.p7 | 15:63673265 | AAACATAACTAAAAT[A/G]TGAGTTGCTACAAAG | 8925 |
rs55679015 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | HERC1 | GRCh38.p7 | 15:63787627 | TTATAGAGCCAGACT[C/T]GGTGGCACACATCTA | 8925 |
rs55724483 | snp | G/T | 0.0667028 | 0.170006 | intron-variant | HERC1 | GRCh38.p7 | 15:63802269 | TGTGCAAAATTGAAC[G/T]CCTGCTAAAAAAGAA | 8925 |
rs55762773 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63789154 | GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 8925 |
rs55820694 | snp | C/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63731465 | TATTCCTTTCAACTT[C/T]GTTGTAACATTCCTT | 8925 |
rs55892920 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63827241 | ACCAGCCTGGGCAAC[A/C]TGACAAAACCCCATC | 8925 |
rs55941923 | snp | C/T | 0.205723 | 0.246048 | intron-variant | HERC1 | GRCh38.p7 | 15:63683367 | TTGCTATGATTTTTT[C/T]CTATTGGAGTCTCTG | 8925 |
rs55955845 | snp | A/G | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63770312 | GTCCCTTTGCCTCCC[A/G]CCCTCTTCTTTCATC | 8925 |
rs55989641 | snp | A/G | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63777303 | TAAGATACTTGTAAA[A/G]TATGCACTTAAGAGG | 8925 |
rs56019571 | snp | A/G | 0.287867 | 0.247116 | intron-variant | HERC1 | GRCh38.p7 | 15:63745240 | GCGGGGGGTGAGCCA[A/G]CACTCCCTTGGTTAC | 8925 |
rs56045405 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | HERC1 | GRCh38.p7 | 15:63801713 | TCTCACATATTATCT[C/T]ACTCTGAACTGACCT | 8925 |
rs56070389 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | HERC1 | GRCh38.p7 | 15:63741271 | TGACCTCGTGATCCA[C/T]CCGCCTCAGCCTCTC | 8925 |
rs56076127 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829499 | ATATATATATATATA[C/T]ACACACACACACATA | 8925 |
rs56090710 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGTGTGTCTCTCT | | | intron-variant | HERC1 | GRCh38.p7 | 15:63744138 | TGTGTGTGTGTGTGT[lengthTooLong]CTCTCTCTCTCTCTC | 8925 |
rs56100886 | snp | A/G | 0.366266 | 0.221319 | intron-variant | HERC1 | GRCh38.p7 | 15:63789013 | GTTGAGATGTTAAAA[A/G]TAAACTTGATAAAAT | 8925 |
rs56113145 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | HERC1 | GRCh38.p7 | 15:63829157 | GGTACTGTGGCTCAC[A/G]CATGGAATCCCAACA | 8925 |
rs56117020 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | HERC1 | GRCh38.p7 | 15:63742393 | TGAGTGTGTGTGTGT[C/T]CCTTAGAATTTTCTA | 8925 |
rs56122265 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | HERC1 | GRCh38.p7 | 15:63810621 | TAACATTTGCATATA[C/T]TGCTTCTTTTTTTTA | 8925 |
rs56140097 | snp | C/T | 0.462253 | 0.132093 | intron-variant | HERC1 | GRCh38.p7 | 15:63776999 | TATATTTTTTATATA[C/T]ACACAAAATTTTTAA | 8925 |
rs56163012 | snp | C/G | 0.206642 | 0.246211 | intron-variant | HERC1 | GRCh38.p7 | 15:63651758 | ACTATTAAAAATGCG[C/G]CTGGGCGTAGTGGCT | 8925 |
rs56169805 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC1 | GRCh38.p7 | 15:63731920 | CAACAGGAAATACGT[A/G]TACAATGTACAATTC | 8925 |
rs56174010 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | HERC1 | GRCh38.p7 | 15:63716710 | TTTGATTAAAATATC[A/G]TGCTGTAAATTTATT | 8925 |
rs56175545 | snp | C/T | 0.205723 | 0.246048 | intron-variant | HERC1 | GRCh38.p7 | 15:63696797 | ATTAATAAGTTTATA[C/T]AGAATGAATACTCTT | 8925 |
rs56196711 | in-del | -/TTT | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63757282 | TTTTTTTTTTTTTTT[-/TTT]GAGACAGAGTCTCGC | 8925 |
rs56221233 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | HERC1 | GRCh38.p7 | 15:63651924 | ACCTGTAGTCCCAGC[C/T]TCTTGGGAAGAGAAG | 8925 |
rs56318707 | snp | A/C/T | 8.97826e-05 | 0.00669957 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63656169 | TGTGCTCAAATAGGC[A/C/T]AGGCAAGAGATAGGC | 8925 |
rs56329950 | in-del | -/A | 0.47726 | 0.104176 | intron-variant | HERC1 | GRCh38.p7 | 15:63673254 | ATCCTACAAATAAAC[-/A]TAACTAAAATATGAG | 8925 |
rs56333803 | snp | C/G | 0.210909 | 0.246925 | intron-variant | HERC1 | GRCh38.p7 | 15:63646607 | GAATTCGAGACCAGC[C/G]TGGCCAGCATGGTGA | 8925 |
rs56388539 | snp | C/T | 0.4628 | 0.13121 | intron-variant | HERC1 | GRCh38.p7 | 15:63676747 | GGCGACAGAGCGAGA[C/T]TCCGTCTCAAAAAAA | 8925 |
rs56661159 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63696951 | AAAAAAAAAAAAAAA[-/A]TTATTTTGAAATAAT | 8925 |
rs56703723 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HERC1 | GRCh38.p7 | 15:63825332 | GCAAGAGCAATATAA[C/T]TAATATTAGCATATT | 8925 |
rs56711653 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | HERC1 | GRCh38.p7 | 15:63701756 | AAATATTTAGTTTGA[C/T]ATCAAAAAGACTTAA | 8925 |
rs56771068 | in-del | -/GTATAT | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829561 | TGTGTGTGTGTGTGT[-/GTATAT]ATATATATATATATA | 8925 |
rs56771388 | snp | A/G | 0.366473 | 0.221211 | intron-variant | HERC1 | GRCh38.p7 | 15:63771991 | GCTGGGCATGGTGGC[A/G]GGTGCCTGTAGTCCC | 8925 |
rs57040637 | in-del | -/A | | | intron-variant | HERC1 | GRCh38.p7 | 15:63698420 | GAAACTCCGTCTCCA[-/A]AAAAAAAAAAAAAAA | 8925 |
rs57080812 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63768688 | TTTATGCCTTTCTAC[-/A]AGTATGGAGAAAAAT | 8925 |
rs57121923 | in-del | -/A | 0.375 | 0.216506 | intron-variant | HERC1 | GRCh38.p7 | 15:63730047 | AAAAAAAAAAAAAAA[-/A]GCATTATATCCTTTC | 8925 |
rs57329632 | snp | A/G | 0.31503 | 0.241394 | intron-variant | HERC1 | GRCh38.p7 | 15:63830183 | TGTATGAACAATAAA[A/G]GGAAGAATAGTAACT | 8925 |
rs57342146 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63621634 | AGGTACACCAATCAG[A/G]TGTAGATTTGGTCTT | 8925 |
rs57628136 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | HERC1 | GRCh38.p7 | 15:63621783 | CCAGTTGATCGAATC[A/G]GTTACTGAGGCTTGT | 8925 |
rs57634390 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63821754 | AAAAAAAAAAAATCA[A/G]ATAATCTAATTTAGA | 8925 |
rs57652025 | snp | A/G | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63741502 | TTATTTAGTAGATAC[A/G]GGGTTTCACCATGTT | 8925 |
rs57723091 | snp | C/G | 0.221439 | 0.248363 | intron-variant | HERC1 | GRCh38.p7 | 15:63683434 | AGATGGAGATATAGA[C/G]ATATGCTTTTAGAGT | 8925 |
rs57738617 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63742856 | GGATTTGGTTTGTTA[C/G]TAGTTTGTTGAGAAT | 8925 |
rs57817022 | snp | A/G | 0.109461 | 0.206758 | intron-variant | HERC1 | GRCh38.p7 | 15:63824852 | GACGTAGGAAAAAAA[A/G]AAAACACTAAATGAT | 8925 |
rs58100964 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | HERC1 | GRCh38.p7 | 15:63701900 | TATATCTGAAAAGGG[C/T]ATTAAAAGCTTCTAC | 8925 |
rs58170614 | in-del | -/C | 0.0991586 | 0.199366 | intron-variant | HERC1 | GRCh38.p7 | 15:63802601 | TAAAAGCCAATTGTT[-/C]TTTTTTCCACTCCTG | 8925 |
rs58601053 | in-del | -/AA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63769427 | TCTGTTTCCAAAAAA[-/AA]CAGGGCTAAAGCTGG | 8925 |
rs58622525 | in-del | -/TG | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63829460 | GTGTGTGTGTGTGTG[-/TG]CACATATATGTTTAT | 8925 |
rs58633453 | in-del | -/C | 0.483708 | 0.088773 | intron-variant | HERC1 | GRCh38.p7 | 15:63646835 | ACAAACAAACAAAAA[-/C]AAAAACAAAACAAAA | 8925 |
rs58698103 | in-del | -/CA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63755132 | TAACAAAATAAATGA[-/CA]GTCTTTGGCCTAGTA | 8925 |
rs58882575 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | HERC1 | GRCh38.p7 | 15:63788422 | AAGCCCTGATTGTTT[C/T]AAGGAAGAATTCTAT | 8925 |
rs58928856 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HERC1 | GRCh38.p7 | 15:63782886 | AGTGGAGGAAGTAAC[C/T]GCAGACGTGGTGGAA | 8925 |
rs58984935 | in-del | -/GT/GTGTGTGTGTGTGTCT | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63744165 | TGTGTGTGTGTGTGT[-/GT/GTGTGTGTGTGTGTCT]CTCTCTCTCTCTCTC | 8925 |
rs58989752 | in-del | -/AA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63704116 | CAAAAAAGGAAAAAA[-/AA]TACAGTCATTTATTT | 8925 |
rs59014847 | in-del | -/AATATATATA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829479 | ATATATGTTTATATA[-/AATATATATA]TATATATATATACAC | 8925 |
rs59107973 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | HERC1 | GRCh38.p7 | 15:63741305 | GTGCTGGGATTACAG[A/G]CGTGAGCCACCGCGC | 8925 |
rs59109042 | in-del | -/T | 0.486332 | 0.08153 | intron-variant | HERC1 | GRCh38.p7 | 15:63736613 | TAGCATCACACTCTC[-/T]TTTTTTTTTTTTGAG | 8925 |
rs59224907 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63638865 | TTCTAATCATTAAGT[C/G]TTATTTCCAAAAAAG | 8925 |
rs59241163 | in-del | -/TT | | | intron-variant | HERC1 | GRCh38.p7 | 15:63644509 | CTTTGTTTTTTTTTT[-/TT]CTGTTTTTGCTTTTT | 8925 |
rs59274228 | snp | A/G | 0.364193 | 0.222396 | intron-variant | HERC1 | GRCh38.p7 | 15:63733857 | ACCCTGTCTCAAAAA[A/G]AAAAATAAAAAAATC | 8925 |
rs59274412 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63789147 | CCAGGCTGGAGTGCA[A/G]TGGTGCAATCTCGGC | 8925 |
rs59284373 | snp | A/G | 0.312104 | 0.242163 | intron-variant | HERC1 | GRCh38.p7 | 15:63724428 | CATATTTGGAAATGG[A/G]GGAAAATCCTCAACT | 8925 |
rs59288964 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63807794 | CAATCCTACCTTTGT[-/G]CCCCCACTCATGCTG | 8925 |
rs59407137 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | HERC1 | GRCh38.p7 | 15:63828861 | AACTTTGGAAAACTA[C/T]TTTGACTAGATACTA | 8925 |
rs59408197 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | HERC1 | GRCh38.p7 | 15:63616034 | TTTTAAGGATAAAAA[A/C]AAGGAACACAAAACA | 8925 |
rs59436795 | in-del | -/CAA | | | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63835430 | CATACTCAAAAACAA[-/CAA]GCAAAAGCTCCTCCT | 8925 |
rs59546664 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63787958 | AGGGTGAGACCCTGT[C/T]TCAAAAAAAAAAAAA | 8925 |
rs59561105 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | HERC1 | GRCh38.p7 | 15:63651756 | AAACTATTAAAAATG[C/T]GGCTGGGCGTAGTGG | 8925 |
rs59580148 | in-del | -/CA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829511 | ATATACACACACACA[-/CA]TATATAAATAATATG | 8925 |
rs59619536 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63806794 | CCACCCACTCCGAGA[C/T]AGTCTTGCTCTGTCA | 8925 |
rs59766681 | snp | A/G | 0.157311 | 0.232183 | intron-variant | HERC1 | GRCh38.p7 | 15:63633432 | ACTCAGATTTCCTTT[A/G]TATTGTTTTCTTAAA | 8925 |
rs59769375 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63815554 | GCCTCTCTAAAAGTG[C/T]AATGCTTACAGGCTA | 8925 |
rs59781628 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | HERC1 | GRCh38.p7 | 15:63751172 | GACCACATTATACAA[A/C]AGTGGTCCCTTAAGA | 8925 |
rs59809979 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | HERC1 | GRCh38.p7 | 15:63661376 | AGATAATATTTTTAT[A/G]GAACTCGTTTAATCA | 8925 |
rs59909117 | in-del | -/GT | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829541 | TGTGTGCACATATAT[-/GT]ATGTGTGTGTGTGTG | 8925 |
rs60037018 | in-del | -/TA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829594 | ATATATATATATATA[-/TA]ATATACTGATATATT | 8925 |
rs60055564 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63802069 | CAATAAAGACTTCTC[A/G]AGGGCATTTCTGAAA | 8925 |
rs60213089 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | HERC1 | GRCh38.p7 | 15:63827454 | CGAAGAAAATGAAAG[C/G]AATATCTCTTCAAAA | 8925 |
rs60219663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63743016 | TGGGAAGTATTAGCT[C/T]CTCTTCTACATTCTG | 8925 |
rs60282704 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | HERC1 | GRCh38.p7 | 15:63800325 | AAGGCCAAGAACTGA[C/T]CTCTCCCCTTGCTCT | 8925 |
rs60312843 | snp | A/T | 0.480853 | 0.0959518 | intron-variant | HERC1 | GRCh38.p7 | 15:63786920 | ACTCAATAAATTATT[A/T]TTTTTTTTTTTTTTA | 8925 |
rs60407607 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63828489 | GGATTACAGGCAAGC[A/G]CCACCACACCAAGCT | 8925 |
rs60498045 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63808012 | TTACCCTATATGGTC[C/T]CTAATTGTTCATCAT | 8925 |
rs60572942 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | HERC1 | GRCh38.p7 | 15:63742684 | TATCATGAAAGAATG[A/T]TGAATTTTGTCAGAT | 8925 |
rs60576753 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HERC1 | GRCh38.p7 | 15:63701964 | TAATTCAGAATCACC[C/T]ACTATATAAAGAAAA | 8925 |
rs60603260 | snp | A/C | 0.166832 | 0.235761 | intron-variant | HERC1 | GRCh38.p7 | 15:63687567 | AAGAAATAGTGAGGG[A/C]CTGAATTCATTCATT | 8925 |
rs60618359 | snp | G/T | 0.202959 | 0.245534 | intron-variant | HERC1 | GRCh38.p7 | 15:63615253 | CCAATTCAGAACCGA[G/T]TTAAGGCACTGGGTA | 8925 |
rs60769955 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HERC1 | GRCh38.p7 | 15:63699380 | TAAGACACTGCTAGT[A/C]AGACCTACTCAAAAC | 8925 |
rs60779579 | snp | C/T | 0.202035 | 0.245356 | intron-variant | HERC1 | GRCh38.p7 | 15:63638965 | AGTATTTCCCTTTAT[C/T]ATAAACACTTTCACT | 8925 |
rs60788174 | in-del | -/TG | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829531 | TAAATAATATGTGTG[-/TG]CACATATATGTATGT | 8925 |
rs60841389 | in-del | -/AA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63795087 | AAAAAAAAAAAAAAA[-/AA]GTAAAGGAATAATCA | 8925 |
rs60954093 | snp | A/C | 0.205723 | 0.246048 | intron-variant | HERC1 | GRCh38.p7 | 15:63683355 | ACTGGTGGGTTTTTG[A/C]TATGATTTTTTCCTA | 8925 |
rs61054895 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HERC1 | GRCh38.p7 | 15:63779932 | GGCAGGAGAATCGCT[C/T]GAACCCGGGAGGTGG | 8925 |
rs61059171 | snp | C/T | 0.20511 | 0.245937 | intron-variant | HERC1 | GRCh38.p7 | 15:63625030 | ATTATAAACATTTCT[C/T]CCACTAATTACAGTT | 8925 |
rs61082744 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63801860 | CCCAAGGCTTTTACC[C/T]ATCTCATATGCTAAT | 8925 |
rs61100980 | in-del | -/CTCTA | 0.0414363 | 0.137845 | intron-variant | HERC1 | GRCh38.p7 | 15:63764751 | AGTGGTTAACTGTCT[-/CTCTA]AAACAATAATTGACT | 8925 |
rs61107158 | snp | C/G | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63745749 | TTGGTTCTTATGAAG[C/G]TGGTTTTTTCTGTGT | 8925 |
rs61138406 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63711117 | AGCAGGAGGATCACT[G/T]GAGGCCAGGAGTTTA | 8925 |
rs61154847 | in-del | -/CA/CACATACA/CATACA/CATACC/TACC | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63718124 | ACACACACACACACA[lengthTooLong]ACCCCCTCCTTGGTT | 8925 |
rs61230381 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | HERC1 | GRCh38.p7 | 15:63781821 | TTAAAGAAACCAAGA[A/G]AGCCACTCCAATGAA | 8925 |
rs61238562 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | HERC1 | GRCh38.p7 | 15:63784486 | TTTTTTTAAAACCTA[-/G]GAACACTAGTTGCCT | 8925 |
rs61255042 | in-del | -/A | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63824549 | AAAAAAAAAAAAAAA[-/A]TTAAAAAGAAAACCA | 8925 |
rs61266201 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | HERC1 | GRCh38.p7 | 15:63809913 | TCGAACCCCTGGGTT[C/T]AAGCAATCCTGCCTC | 8925 |
rs61281873 | in-del | -/CCAA | | | intron-variant | HERC1 | GRCh38.p7 | 15:63800889 | TGCCAGAGAAACCAA[-/CCAA]GTGATAAAAGTGTTG | 8925 |
rs61293253 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63826056 | GGTGTGAGCCACCAC[A/G]CCCGGCCAAATAATA | 8925 |
rs61303059 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63789087 | TAAAAGGTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 8925 |
rs61330449 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63820695 | TATCCTTTTTTTTTT[-/T]GCTTTTGAGACAAGG | 8925 |
rs61336273 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC1 | GRCh38.p7 | 15:63733226 | TCCCAGAAAAAAACT[A/G]TACTAATCCACTTAC | 8925 |
rs61341328 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | HERC1 | GRCh38.p7 | 15:63675786 | AAAGCTTTTGCTGGT[A/G]TAAAGTTTTGTTGTT | 8925 |
rs61362807 | in-del | -/AT | | | intron-variant | HERC1 | GRCh38.p7 | 15:63829468 | TGTGTGTGCACATAT[-/AT]GTTTATATAAATATA | 8925 |
rs61385516 | snp | A/G | 0.32955 | 0.237006 | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63834289 | GGGTGGTGAGGAGTG[A/G]GGGGCCATGCAGTGC | 8925 |
rs61426575 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | HERC1 | GRCh38.p7 | 15:63617185 | CCCACAACAGGCCCC[A/G]GTGTGTGATGTTCCC | 8925 |
rs61431709 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63789092 | GGTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 8925 |
rs61498040 | in-del | -/G | 0.061206 | 0.163881 | intron-variant | HERC1 | GRCh38.p7 | 15:63664449 | CTTTCACAAAGAAAA[-/G]GATACGGAACATAAA | 8925 |
rs61570739 | in-del | -/A | 0.21875 | 0.248039 | intron-variant | HERC1 | GRCh38.p7 | 15:63662843 | TCAAAGTAACCTCAT[-/A]ACTTTAAATCCCCAA | 8925 |
rs61738787 | snp | A/G | 0.00821926 | 0.0635773 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63649749 | GATAGCAATGCTCCA[A/G]TTCTCGACGGTGCAT | 8925 |
rs61740231 | snp | C/T | 4.96808e-05 | 0.00498377 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63645019 | TTCCTGCTCCCACCA[C/T]CCTTCTGCACTAGTC | 8925 |
rs61740450 | snp | G/T | 0.0411861 | 0.137466 | missense | HERC1 | GRCh38.p7 | 15:63729277 | TTCCAAGGACTTTCT[G/T]TGAGCAAATTTGCAG | 8925 |
rs61745864 | snp | C/T | 0.0116804 | 0.0755234 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63746981 | ATTTCGAAGTGGACC[C/T]GCCTGCCTCCCGAGA | 8925 |
rs61749474 | snp | A/G | 0.0510936 | 0.151447 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63713523 | ATCCTGACCCTCAGG[A/G]AGGTCTGTGCTGACC | 8925 |
rs61751108 | snp | A/G | 0.0134341 | 0.080849 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63616655 | CATTAAGTGTTCATC[A/G]AGGCAGGCAGAAGGG | 8925 |
rs61751109 | snp | A/G | 0.0123394 | 0.077572 | intron-variant | HERC1 | GRCh38.p7 | 15:63729654 | AATGCTTGATCCTAA[A/G]ATGACACACAAAGGA | 8925 |
rs61751110 | snp | A/G | 0.00684029 | 0.0580806 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63758268 | GCTATTGCTCCCCCA[A/G]ACATAAACCTCACAG | 8925 |
rs62012360 | snp | C/T | 0.359152 | 0.224913 | intron-variant | HERC1 | GRCh38.p7 | 15:63705336 | TTTTTTTCTTTTTGG[C/T]AGAGACAGGGGTCTC | 8925 |
rs62012361 | snp | A/C | 0.311123 | 0.242413 | intron-variant | HERC1 | GRCh38.p7 | 15:63707959 | AAAAAAAAAAGAAGA[A/C]GTGACAAAACAGATT | 8925 |
rs62012362 | snp | A/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63709804 | TCTAGTGGGTTTACT[A/G]GGAAGACATACTAAT | 8925 |
rs62012363 | snp | A/G | 0.266 | 0.249487 | intron-variant | HERC1 | GRCh38.p7 | 15:63717248 | ATGAGTTTCAAATAT[A/G]AGCCTCAACAAAATG | 8925 |
rs62012364 | snp | A/C | 0.176219 | 0.238865 | intron-variant | HERC1 | GRCh38.p7 | 15:63720975 | ATAAAGTCTATGCTT[A/C]CAGTGTATAAGCAAT | 8925 |
rs62012365 | snp | A/G | 0.174932 | 0.238463 | intron-variant | HERC1 | GRCh38.p7 | 15:63723131 | TGCATATATATTTGC[A/G]AGCATTATGAGCTAA | 8925 |
rs62012817 | snp | G/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63610331 | AGGGAGGTGCCACTA[G/T]GTGGCTCTGATGACC | 8925 |
rs62012818 | snp | C/G | 0.203267 | 0.245593 | intron-variant | HERC1 | GRCh38.p7 | 15:63612081 | TAGTCCCAGCTACTG[C/G]GGAGGCTGAGGCAGG | 8925 |
rs62012820 | snp | G/T | 0.270333 | 0.249172 | intron-variant | HERC1 | GRCh38.p7 | 15:63616388 | TAGTCTGTGCATATA[G/T]GACGTCAACACCAGT | 8925 |
rs62012822 | snp | A/G | 0.17461 | 0.238362 | intron-variant | HERC1 | GRCh38.p7 | 15:63622353 | TTTTTTTTGAGATGT[A/G]GTCTCGCTCTGTTGC | 8925 |
rs62012823 | snp | A/G | 0.17461 | 0.238362 | intron-variant | HERC1 | GRCh38.p7 | 15:63623150 | TAGTGGTGGCTGTGA[A/G]AAGAGTGTAGTGATG | 8925 |
rs62012824 | snp | C/T | 0.17461 | 0.238362 | intron-variant | HERC1 | GRCh38.p7 | 15:63623327 | ATTTTAAGACCAGTT[C/T]GTAACTTTATTTTTC | 8925 |
rs62012825 | snp | G/T | 0.177824 | 0.239355 | intron-variant | HERC1 | GRCh38.p7 | 15:63626369 | AAAAATAAAATAAAA[G/T]AAAATGTCTTCATTA | 8925 |
rs62012826 | snp | A/G | 0.177824 | 0.239355 | intron-variant | HERC1 | GRCh38.p7 | 15:63626488 | CAAATTTTTCCTTTC[A/G]TATTTAATAATTGTC | 8925 |
rs62012827 | snp | A/C | 0.198324 | 0.244601 | intron-variant | HERC1 | GRCh38.p7 | 15:63628001 | TGTTTCAAATGGTTA[A/C]CTAAGGTGAGGAATT | 8925 |
rs62012828 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HERC1 | GRCh38.p7 | 15:63629682 | GTGCAACCACAATGA[C/T]GAGCAGCTTCCTTGT | 8925 |
rs62012829 | snp | C/T | 0.204496 | 0.245824 | intron-variant | HERC1 | GRCh38.p7 | 15:63629923 | ATAGAGGAGGGTGAA[C/T]ACATCAACCTCTTGA | 8925 |
rs62012830 | snp | C/T | 0.177503 | 0.239258 | intron-variant | HERC1 | GRCh38.p7 | 15:63632862 | AAGAAAAAAAATCAC[C/T]CTTGAATTTGCCTAA | 8925 |
rs62012831 | snp | A/G | 0.204803 | 0.245881 | intron-variant | HERC1 | GRCh38.p7 | 15:63633519 | ATGCAGAGGGTTACA[A/G]AGGATTACTCATAGT | 8925 |
rs62012832 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63636291 | TTTTTTTTTTTTTTA[G/T]ATGGAGTCTCACTCT | 8925 |
rs62012833 | snp | A/T | 0.205723 | 0.246048 | intron-variant | HERC1 | GRCh38.p7 | 15:63636644 | CACCTAAAATAATGG[A/T]GATGACAAGGAAAAC | 8925 |
rs62012834 | snp | A/G | 0.20511 | 0.245937 | intron-variant | HERC1 | GRCh38.p7 | 15:63636756 | ATTTTCTACTTTCAC[A/G]TAGCACCTATGAAAC | 8925 |
rs62012836 | snp | C/T | 0.204496 | 0.245824 | intron-variant | HERC1 | GRCh38.p7 | 15:63639410 | CGTATAGTCTTGTTG[C/T]AAGTAGGCTGTATCA | 8925 |
rs62012837 | snp | A/T | 0.204496 | 0.245824 | intron-variant | HERC1 | GRCh38.p7 | 15:63639713 | CACTCTCAAATACAA[A/T]CAGAATGAAATGACA | 8925 |
rs62012838 | snp | A/G | 0.177503 | 0.239258 | intron-variant | HERC1 | GRCh38.p7 | 15:63642093 | GTAGAACCTTTCATG[A/G]AGGTTTACAGCTTAT | 8925 |
rs62012839 | snp | A/G | 0.204189 | 0.245767 | intron-variant | HERC1 | GRCh38.p7 | 15:63647612 | CCTAAGTGTCCATCA[A/G]TGGATGACTGGATAA | 8925 |
rs62014163 | snp | C/T | 0.205723 | 0.246048 | intron-variant | HERC1 | GRCh38.p7 | 15:63652715 | TGGAGTGCAGTGGCT[C/T]AATCTCAGCTCACTG | 8925 |
rs62014164 | snp | A/G | 0.178144 | 0.239451 | intron-variant | HERC1 | GRCh38.p7 | 15:63655147 | TCACACGAGGCCAGG[A/G]GTTCAAGACAAGCCT | 8925 |
rs62014165 | snp | A/G | 0.233818 | 0.249476 | intron-variant | HERC1 | GRCh38.p7 | 15:63655157 | CCAGGAGTTCAAGAC[A/G]AGCCTGGCCAACATG | 8925 |
rs62014166 | snp | C/T | 0.231189 | 0.249291 | intron-variant | HERC1 | GRCh38.p7 | 15:63657395 | TTCTCTGAAGACTCA[C/T]TGAGGTTGAACATCT | 8925 |
rs62014167 | snp | C/G | 0.204189 | 0.245767 | intron-variant | HERC1 | GRCh38.p7 | 15:63657966 | TTTATATGTATGGGT[C/G]AGTTTCTTAACTCTC | 8925 |
rs62014168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC1 | GRCh38.p7 | 15:63657997 | TTCTGTACTATCCTA[C/T]TTGCCTATCCTTGAG | 8925 |
rs62014169 | snp | G/T | 0.222333 | 0.248464 | intron-variant | HERC1 | GRCh38.p7 | 15:63658969 | ATACTTAATTTACCA[G/T]TAAGTATTTTCTGTT | 8925 |
rs62014170 | snp | C/T | 0.222928 | 0.24853 | intron-variant | HERC1 | GRCh38.p7 | 15:63659203 | AAATAACAAGTTCTA[C/T]AAATCTTTTTATTGC | 8925 |
rs62014171 | snp | C/T | 0.180383 | 0.240111 | intron-variant | HERC1 | GRCh38.p7 | 15:63666723 | CACTCCTCATCCAAG[C/T]TCCATATTTGTAAAT | 8925 |
rs62014172 | snp | C/T | 0.181022 | 0.240296 | intron-variant | HERC1 | GRCh38.p7 | 15:63667112 | GATGAGCTATAGTGT[C/T]GGTGGCCATAAGCTC | 8925 |
rs62014173 | snp | C/T | 0.206336 | 0.246157 | intron-variant | HERC1 | GRCh38.p7 | 15:63667247 | AGAAGTTCACAGGAA[C/T]TTAACCCTGTATTTC | 8925 |
rs62014174 | snp | C/T | 0.206336 | 0.246157 | intron-variant | HERC1 | GRCh38.p7 | 15:63669807 | GACTAAACAGGTTAG[C/T]TATAGTTTAATGGAG | 8925 |
rs62014176 | snp | C/T | 0.176219 | 0.238865 | intron-variant | HERC1 | GRCh38.p7 | 15:63673509 | TGTTAACTGCTGTCT[C/T]TCCAGAACCTAAGAA | 8925 |
rs62014177 | snp | A/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63675417 | CAGGAAATATTTTAG[A/T]CTCTGCAGGGCACAC | 8925 |
rs62014178 | snp | G/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63675922 | TTTTTTTTTTTTTTG[G/T]AGACGGAGTCTTGTT | 8925 |
rs62014180 | snp | A/G | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63676751 | ACAGAGCGAGATTCC[A/G]TCTCAAAAAAATAAA | 8925 |
rs62014181 | snp | A/C | 0.031825 | 0.122064 | intron-variant | HERC1 | GRCh38.p7 | 15:63678969 | TTAAATGAGATTATG[A/C]ACATAAAGTGCTTAT | 8925 |
rs62014182 | snp | A/G | 0.175897 | 0.238765 | intron-variant | HERC1 | GRCh38.p7 | 15:63682596 | GGCAAGAAAGCAAGA[A/G]CCCCATCTCTACAAA | 8925 |
rs62014183 | snp | G/T | 0.220843 | 0.248294 | intron-variant | HERC1 | GRCh38.p7 | 15:63682676 | TTCTTAAGCTGAGCT[G/T]TTGCTATTGCTACAG | 8925 |
rs62014184 | snp | C/T | 0.220843 | 0.248294 | intron-variant | HERC1 | GRCh38.p7 | 15:63682677 | TCTTAAGCTGAGCTT[C/T]TGCTATTGCTACAGC | 8925 |
rs62014185 | snp | C/G | 0.221439 | 0.248363 | intron-variant | HERC1 | GRCh38.p7 | 15:63683063 | ATCCCTTGAAACTGG[C/G]AGGTGGAGGTTGCAG | 8925 |
rs62014212 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | HERC1 | GRCh38.p7 | 15:63683705 | CCAGGCTGGCATGCA[A/G]TAGTGTAAACAGAGC | 8925 |
rs62014213 | snp | C/T | 0.185155 | 0.241444 | intron-variant | HERC1 | GRCh38.p7 | 15:63685325 | CCCCATGGGGGCAGG[C/T]CACATTGGTATCATG | 8925 |
rs62014214 | snp | A/G | 0.208169 | 0.246476 | intron-variant | HERC1 | GRCh38.p7 | 15:63687262 | AATAGTGAGGGGGCC[A/G]GGTGTGGTGGCTCAC | 8925 |
rs62014215 | snp | A/C | 0.224116 | 0.248656 | intron-variant | HERC1 | GRCh38.p7 | 15:63687294 | CTTGTAATCCCAGCA[A/C]TTTGAGAGACCGAAG | 8925 |
rs62014216 | snp | G/T | 0.175576 | 0.238665 | intron-variant | HERC1 | GRCh38.p7 | 15:63691661 | AAAAAAGGAGCAGTT[G/T]TAAGTTATACTAATT | 8925 |
rs62014217 | snp | A/G | 0.178144 | 0.239451 | intron-variant | HERC1 | GRCh38.p7 | 15:63695183 | TGGGACTACAGGCAC[A/G]TACCACCACACTTGG | 8925 |
rs62020761 | snp | A/G | 0.168785 | 0.236441 | intron-variant | HERC1 | GRCh38.p7 | 15:63740624 | TGTCACTTAGTGGGT[A/G]TGAAGTGGTATCTCA | 8925 |
rs62020778 | snp | C/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63744168 | TGTGTGTGTGTGTCT[C/G]TCTCTCTCTCTCTCT | 8925 |
rs62020779 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63747476 | AAAAAAAAAAAATTT[A/T]GTCAAGTCATGAACA | 8925 |
rs62020780 | snp | A/G | 0.26271 | 0.249677 | intron-variant | HERC1 | GRCh38.p7 | 15:63762808 | CACAAAAATATTGCA[A/G]CTAATTGTTGGGAAA | 8925 |
rs62020781 | snp | C/T | 0.169435 | 0.236663 | intron-variant | HERC1 | GRCh38.p7 | 15:63770929 | CACGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 8925 |
rs62020782 | snp | C/T | 0.463126 | 0.13068 | intron-variant | HERC1 | GRCh38.p7 | 15:63773598 | TGTTGCCCAGGAGTG[C/T]TGTGGCATGATCTCT | 8925 |
rs62020784 | snp | C/T | 0.263535 | 0.249633 | intron-variant | HERC1 | GRCh38.p7 | 15:63779831 | CCATCCTTGCCAACA[C/T]GGTGAAACCCCGTCT | 8925 |
rs62020785 | snp | C/T | 0.308414 | 0.24308 | intron-variant | HERC1 | GRCh38.p7 | 15:63784406 | AGTATTTGTGTATAC[C/T]GTAATAGTTCATATA | 8925 |
rs62020786 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63784603 | CATGTATTATCATGC[A/T]AATTTTTTTTTTTTT | 8925 |
rs62020787 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63784620 | ATTTTTTTTTTTTTC[C/T]TTTTTGAGACAGAGT | 8925 |
rs62020789 | snp | C/G | 0.16976 | 0.236773 | intron-variant | HERC1 | GRCh38.p7 | 15:63787676 | AGGCTAAGGCAGGAG[C/G]ATCACTTGAGGCCAG | 8925 |
rs62020791 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63789073 | TAATAAAGCAGGAAT[A/T]AAAGGTTTTTTTTTT | 8925 |
rs62020792 | snp | C/T | 0.469544 | 0.119585 | intron-variant | HERC1 | GRCh38.p7 | 15:63789151 | GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 8925 |
rs62020827 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | HERC1 | GRCh38.p7 | 15:63796689 | CTTGTAAAATGTCCA[C/T]TGATTCAGTCCAGAA | 8925 |
rs62020828 | snp | C/T | 0.307671 | 0.243257 | intron-variant | HERC1 | GRCh38.p7 | 15:63798097 | TCACTAAAGCACTTA[C/T]TTTAGAGAAGTGTGA | 8925 |
rs62020829 | snp | A/G | 0.171704 | 0.237423 | intron-variant | HERC1 | GRCh38.p7 | 15:63804054 | ATAATCTTTTCAACA[A/G]AAGGTGCTGGACCAA | 8925 |
rs62020830 | snp | A/G | 0.0248628 | 0.108689 | intron-variant | HERC1 | GRCh38.p7 | 15:63804993 | CATACACTGCTGGTA[A/G]AAATGTGACATGGGA | 8925 |
rs62020831 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63806164 | CTGCAGAACACAAGT[G/T]GTTTTTTTTTTTTCT | 8925 |
rs62020832 | snp | C/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63806494 | GTTTGTTATTATTTG[C/T]GTACCTGTCTTCATC | 8925 |
rs62020834 | snp | C/G | 0.305934 | 0.243663 | intron-variant | HERC1 | GRCh38.p7 | 15:63828447 | CAGGTTCAAGTGATT[C/G]TCCTGCCTCAGACTC | 8925 |
rs62020835 | snp | C/T | 0.314301 | 0.241589 | intron-variant | HERC1 | GRCh38.p7 | 15:63828498 | GCAAGCGCCACCACA[C/T]CAAGCTAATTTTGTA | 8925 |
rs62020836 | snp | A/G | 0.261332 | 0.249743 | intron-variant | HERC1 | GRCh38.p7 | 15:63828768 | AATGGAACAGTAACA[A/G]TAACAAATGAACTTA | 8925 |
rs62022639 | snp | C/T | 0.177182 | 0.23916 | intron-variant | HERC1 | GRCh38.p7 | 15:63728437 | CTCAGTTTGAAAATA[C/T]TTTAGTTGCTGTGGA | 8925 |
rs62023075 | snp | A/G | 0.331874 | 0.236213 | intron-variant | HERC1 | GRCh38.p7 | 15:63833745 | CGGCAAAGCACACAC[A/G]CGCGCGCGCACACAC | 8925 |
rs63269861 | snp | A/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63784606 | GTATTATCATGCAAA[A/T]TTTTTTTTTTTTCCT | 8925 |
rs67155936 | in-del | -/AGAC | 0.440746 | 0.161604 | intron-variant | HERC1 | GRCh38.p7 | 15:63699771 | TAAAATCTTTACATT[-/AGAC]AGCAAAATGTTAACA | 8925 |
rs67163726 | in-del | -/G | | | intron-variant | HERC1 | GRCh38.p7 | 15:63695026 | TTTACTATATTTCAT[-/G]ATATAAAGTATATAA | 8925 |
rs67215903 | in-del | -/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63816097 | CAGCCAAACCATATA[-/C]CCTAACATTTCCCAA | 8925 |
rs67507374 | snp | A/T | 0.319616 | 0.240112 | intron-variant | HERC1 | GRCh38.p7 | 15:63746141 | TGATTCGATATATAT[A/T]TTTTTTAATATAGAT | 8925 |
rs67566652 | snp | A/G | 0.477684 | 0.103247 | intron-variant | HERC1 | GRCh38.p7 | 15:63833793 | CACACACACACACAG[A/G]ACCAGGAGGACGGTA | 8925 |
rs67875794 | snp | C/T | 0.442655 | 0.159323 | intron-variant | HERC1 | GRCh38.p7 | 15:63782401 | CTACTAATCCAACAA[C/T]GAAGCCTGGATGACA | 8925 |
rs71131175 | in-del | -/AT | 0.26326 | 0.249648 | intron-variant | HERC1 | GRCh38.p7 | 15:63637401 | GCTAGATAAAATCAT[-/AT]CAGGTTTTCACTTAC | 8925 |
rs71131176 | in-del | -/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63707953 | TTTTGTCACTTCTTC[-/T]TTTTTTTTTTTTTTT | 8925 |
rs71131177 | in-del | -/A | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63743281 | AGTGAGACTCCATTT[-/A]AAAAAAAAAAAAAAA | 8925 |
rs71131178 | in-del | -/A | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63789108 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8925 |
rs71287038 | in-del | -/ATTTATTTATTT | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63789837 | TAGAATATATAATAC[-/ATTTATTTATTT]ATTTATTTATTTATT | 8925 |
rs71287039 | in-del | -/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63776053 | TTTTTTAACATAAAC[-/T]TTTTTTTTTTTTTTT | 8925 |
rs71287040 | in-del | -/TT | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63706052 | AACTGGTACTGCTGC[-/TT]TTTTTTTTTTTTTTT | 8925 |
rs71287041 | in-del | -/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63646505 | CTTCTTGGTTTTTTT[-/T]TTTTTTTAGCCTCTA | 8925 |
rs71394521 | snp | C/T | 0.459914 | 0.13578 | intron-variant | HERC1 | GRCh38.p7 | 15:63618116 | AATGCCTAGGCTTTC[C/T]TCTAGGGTTTTTATG | 8925 |
rs71394522 | snp | A/C | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63626832 | ATTGTTCGTAGTAAA[A/C]ACTAACATTTACTGA | 8925 |
rs71394523 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC1 | GRCh38.p7 | 15:63652325 | TTCAAAAAATTTTAG[C/T]GACAATATGATTACA | 8925 |
rs71394524 | snp | A/G | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63731939 | AATGTACAATTCTGG[A/G]AAAGGATGATTTCAG | 8925 |
rs71394525 | snp | A/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63786917 | TCAACTCAATAAATT[A/T]TTATTTTTTTTTTTT | 8925 |
rs71394526 | snp | A/G | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63787982 | AAAAAAAAAAAAAAA[A/G]GACAAAACAAAACAA | 8925 |
rs71394527 | snp | G/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63831099 | GTAGACCTTTGTTGT[G/T]GTTTGTTTTGTTTTA | 8925 |
rs71447346 | in-del | -/C | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63697420 | TTACACTATATCGAC[-/C]ATGACTTAATACAGG | 8925 |
rs71447347 | in-del | -/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63697445 | ACAGGTGATGTTAAT[-/T]CTTGATTTTTTTTTT | 8925 |
rs71447349 | in-del | -/A | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63707929 | GCAAGACTCCCTCTC[-/A]AAAAAAAAAAAAAAA | 8925 |
rs71447350 | in-del | -/TTTT | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63739216 | TTTTTTTTTTTTTTT[-/TTTT]AGATGGAGACTCGTT | 8925 |
rs71447352 | in-del | -/G | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63767675 | CGCACTCCAGCCTGG[-/G]AAACAAGAGCGAGGC | 8925 |
rs71447353 | in-del | -/C | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63792354 | TCAACACACAAAATT[-/C]GGTTCTTACTACATT | 8925 |
rs71447354 | in-del | -/TATATA | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63826843 | ATATATATATATATA[-/TATATA]AAGTATGACAACATA | 8925 |
rs71456333 | in-del | ATATATATATATATATATA/TTTTTTTTT | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63826804 | TATATATATATATAT[ATATATATATATATATATA/TTTTTTTTT]TTTTTTTTTTTTTTT | 8925 |
rs71464534 | multinucleotide-polymorphism | CACAC/GAGAG | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63744168 | AGAGAGAGAGAGAGA[CACAC/GAGAG]ACACACACACACACA | 8925 |
rs72750970 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | HERC1 | GRCh38.p7 | 15:63644333 | GCCACTCAGTGTTTT[A/G]AACAATTTTAAGTTA | 8925 |
rs72750973 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HERC1 | GRCh38.p7 | 15:63649432 | TTTTTCTCTTGGACA[G/T]TCCTAACTTTCAAAG | 8925 |
rs72750978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63659200 | TTTAAATAACAAGTT[C/G]TATAAATCTTTTTAT | 8925 |
rs72750981 | snp | A/T | 0.207864 | 0.246424 | intron-variant | HERC1 | GRCh38.p7 | 15:63691538 | GATACATAAATATGT[A/T]ATTAAAAAATACATA | 8925 |
rs72750985 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HERC1 | GRCh38.p7 | 15:63700843 | AACTGAAAATTCAAA[G/T]AATAATATCATAGAT | 8925 |
rs72750986 | snp | A/C | 0.203267 | 0.245593 | intron-variant | HERC1 | GRCh38.p7 | 15:63704139 | CATTTATTTTACTAT[A/C]ATTTAAAAGCAAAAC | 8925 |
rs72750987 | snp | C/G | 0.205723 | 0.246048 | intron-variant | HERC1 | GRCh38.p7 | 15:63706913 | TAGAGTATTAGAATA[C/G]AAATTCATGTAATTA | 8925 |
rs72750988 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | HERC1 | GRCh38.p7 | 15:63708850 | GCTCCTCTTCATCCA[C/T]CCCAGGCTCTCTGAA | 8925 |
rs72750990 | snp | C/T | 0.204803 | 0.245881 | intron-variant | HERC1 | GRCh38.p7 | 15:63713134 | TGTTGTTTATATATA[C/T]GAAAAATTGTGCCTC | 8925 |
rs72750991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63732118 | CAACTCTCCCACCTC[A/G]GCCTCCTGAGTAGCT | 8925 |
rs72752906 | snp | G/T | 0.211516 | 0.24702 | intron-variant | HERC1 | GRCh38.p7 | 15:63801266 | GGTGAGGGGGTAGTT[G/T]TAGGAACTCCCCCGT | 8925 |
rs72752911 | snp | A/C | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63805947 | GACCCTATCTCAAAA[A/C]AAAAAAAAAAAAACA | 8925 |
rs73441916 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC1 | GRCh38.p7 | 15:63610709 | AGGCAGCACAGGGAG[A/G]AATAGCTTTGGCTAC | 8925 |
rs73441919 | snp | A/G | 0.171704 | 0.237423 | intron-variant | HERC1 | GRCh38.p7 | 15:63611911 | CGCAGAGGGCCAGGC[A/G]TGTTGGCTCACGCCT | 8925 |
rs73441926 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | HERC1 | GRCh38.p7 | 15:63629971 | CAGAGGCTCAGTTTA[A/T]TCCTATAAATAATGG | 8925 |
rs73441927 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | HERC1 | GRCh38.p7 | 15:63630397 | TTCCTAGCTTATCTC[C/T]TTCCCCAACTGAGGA | 8925 |
rs73441933 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | HERC1 | GRCh38.p7 | 15:63641861 | ATAAAATTTGTGAAC[A/T]ACCTCTGATTAGCTG | 8925 |
rs73441952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63651094 | ATGAGCACTTCCTCT[C/T]TAATTTGAAGCACAC | 8925 |
rs73441955 | snp | A/C/G | 0.0770313 | 0.181891 | intron-variant | HERC1 | GRCh38.p7 | 15:63660090 | CTGGGAGGCCGAGGC[A/C/G]ACTGGATCACATGAG | 8925 |
rs73444564 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | HERC1 | GRCh38.p7 | 15:63819135 | ATATAACATAGAAGA[A/C]CACTACTCATACTCT | 8925 |
rs73444589 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | HERC1 | GRCh38.p7 | 15:63830386 | AACCCAAAATGAAAG[A/G/T]AGTTCTAAAAAATAA | 8925 |
rs73444597 | snp | C/T | 0.215446 | 0.2476 | upstream-variant-2KB | HERC1 | GRCh38.p7 | 15:63834304 | GGGGGCCATGCAGTG[C/T]GCCCCCTTTTCCTCG | 8925 |
rs73448157 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HERC1 | GRCh38.p7 | 15:63679061 | TCTCAGAGGTTCTAA[A/G]ATTTATCAAAAATGC | 8925 |
rs73448158 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HERC1 | GRCh38.p7 | 15:63679242 | GTATCAGGCACTGGG[C/T]TGCATCTTTACTTCA | 8925 |
rs73448174 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | HERC1 | GRCh38.p7 | 15:63702719 | AGAACAATGCTCATA[C/T]AGTAAGTAGTTTATA | 8925 |
rs73448187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63711879 | AGGTCATAGCACATA[C/T]AGAATCACACACAAG | 8925 |
rs73448191 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | HERC1 | GRCh38.p7 | 15:63716075 | GCAGGTACTGACATT[C/G]CTGCTTCCAGAGCTT | 8925 |
rs73450258 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HERC1 | GRCh38.p7 | 15:63727493 | AATAAAATAAGAGGA[C/T]TTACTTAAATTTGAA | 8925 |
rs73450271 | snp | A/G | 0.321053 | 0.23969 | intron-variant | HERC1 | GRCh38.p7 | 15:63737299 | AAGGAGTTCCAGAGA[A/G]AAAGAAAGAACACAG | 8925 |
rs73450280 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | HERC1 | GRCh38.p7 | 15:63745219 | CCTGGCATTGGGGTC[A/G]GGGAGGCGGGGGGTG | 8925 |
rs73450299 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HERC1 | GRCh38.p7 | 15:63758814 | AGTCATGCAAATCCA[C/T]GCCTACCTAGTCTTC | 8925 |
rs73455397 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | HERC1 | GRCh38.p7 | 15:63780948 | TAAATCTAATAAGTA[A/T]ATCATTTTTTAAATG | 8925 |
rs73457117 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | HERC1 | GRCh38.p7 | 15:63787582 | AAAAAAAGTTCGCTA[C/T]ATCAAGAATGACTTT | 8925 |
rs73457121 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | HERC1 | GRCh38.p7 | 15:63791401 | ACGAGCTCTGTGTAT[A/G]TTCTGAAGATGCCTT | 8925 |
rs73457137 | snp | C/G | 0.306431 | 0.243548 | intron-variant | HERC1 | GRCh38.p7 | 15:63802964 | CCTATAATCCCAACA[C/G]TTCGGGAGGCCAAGG | 8925 |
rs73457142 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HERC1 | GRCh38.p7 | 15:63808329 | GTCTTGCTCTGTTGC[C/T]TAGATTAGACTGCAG | 8925 |
rs74018146 | snp | A/G | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63611128 | AAAGCAGAGGGAACA[A/G]GTTACATAAAAGCAC | 8925 |
rs74018151 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HERC1 | GRCh38.p7 | 15:63627188 | TGTTTGGCATCTACC[C/T]GGAATTCCCACTTTT | 8925 |
rs74018152 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63630201 | TTAACAGTGTATGAG[G/T]ACACACACATAAATA | 8925 |
rs74018158 | snp | A/G | 0.198944 | 0.244731 | intron-variant | HERC1 | GRCh38.p7 | 15:63632442 | TGTCAAGGGCAGTAG[A/G]AAAGAAGAGGGGACG | 8925 |
rs74018159 | snp | C/T | 0.031825 | 0.122064 | intron-variant | HERC1 | GRCh38.p7 | 15:63634672 | CTGAGGGTGTCTAAG[C/T]GAACACAGAAGAAAT | 8925 |
rs74018582 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63657751 | CAATAAACTTTATTG[A/C]TTTATTTTTCTTTTA | 8925 |
rs74018584 | snp | A/C/G | 0.0925924 | 0.197786 | intron-variant | HERC1 | GRCh38.p7 | 15:63671448 | ATTCTTTGAACAGAC[A/C/G]CACCTCCTGAAACTA | 8925 |
rs74019003 | snp | G/T | 0.0704125 | 0.17392 | intron-variant | HERC1 | GRCh38.p7 | 15:63735174 | TTTCATGAGCCTACA[G/T]TCTAATGGGAAAGAA | 8925 |
rs74019004 | snp | C/T | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63744787 | ACAGGTCTAGAAATG[C/T]CATCTAACAATCAAG | 8925 |
rs74019006 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | HERC1 | GRCh38.p7 | 15:63746754 | TGGCATCTGACCTTT[A/G]TCTCAAGGATGAGTT | 8925 |
rs74019007 | snp | A/G | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63748899 | ACAGTTAGCACTTTC[A/G]GAAAAAGCTAAGTTT | 8925 |
rs74019008 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | HERC1 | GRCh38.p7 | 15:63754800 | CAATCATTTCTAACA[C/T]CTTCTCAATCTTCCA | 8925 |
rs74019009 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | HERC1 | GRCh38.p7 | 15:63755086 | AATCTAGGTCTTATC[C/T]ATATAAAATTATCTT | 8925 |
rs74019010 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63758764 | TTAACACAGTCACCA[C/T]AGAGGATACATAAAA | 8925 |
rs74019011 | snp | G/T | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63763605 | TTTAATGGGCAAGAC[G/T]ATAGTGTCTAAGGAT | 8925 |
rs74019013 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | HERC1 | GRCh38.p7 | 15:63779357 | ATCCTAAAGACCTCC[A/G]AGCAAAGAGATGAAA | 8925 |
rs74019014 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63781184 | ATAAAACAATGAAGC[A/G]GAAACCACAGAGAAT | 8925 |
rs74019015 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | HERC1 | GRCh38.p7 | 15:63781365 | ATTTTTCCAAAAGTA[C/G]GTGTTCACTTCATGT | 8925 |
rs74019017 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63790966 | CTTTATAGAAGGCTT[C/G]TTTTTACGAACATCA | 8925 |
rs74019019 | snp | A/T | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63796290 | GTTACATCTTCTGCA[A/T]CTTTTAATAAGTTTC | 8925 |
rs74019020 | snp | C/T | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63798286 | CTGATGTTACTCCCT[C/T]AGTGAAAACCCCAAA | 8925 |
rs74019021 | snp | A/G | 0.0686155 | 0.17228 | intron-variant | HERC1 | GRCh38.p7 | 15:63798418 | CCCTCTCCCACCTAC[A/G]TAACAGACACTTAAG | 8925 |
rs74019022 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HERC1 | GRCh38.p7 | 15:63801285 | GAACTCCCCCGTTTG[C/T]AGGCAATTCAGAAGT | 8925 |
rs74019023 | snp | A/T | 0.0663309 | 0.169604 | intron-variant | HERC1 | GRCh38.p7 | 15:63803645 | TGAACCAATTGCCAA[A/T]TCAGTTCCTTCTTAA | 8925 |
rs74019025 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | HERC1 | GRCh38.p7 | 15:63811911 | GTTTTTCTATTGTTA[A/G]CCATGTTCTTCCTGA | 8925 |
rs74019026 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63812047 | TCCATCTCTATAAAT[G/T]TAGAGCCAGATTTGT | 8925 |
rs74019027 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63812180 | GATGACAAGTTTACT[C/T]AGGGTTGTGTTTTTA | 8925 |
rs74019028 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HERC1 | GRCh38.p7 | 15:63812621 | GAAAATAAATCCATC[C/T]CTGTGGAACTCATGA | 8925 |
rs74019029 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | HERC1 | GRCh38.p7 | 15:63813024 | GAATAGCTAAAAACA[C/T]ACACCTTACCATCAA | 8925 |
rs74019030 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | HERC1 | GRCh38.p7 | 15:63813266 | TTACAACACAACAGG[C/T]TCTTTTCCCTCCCAC | 8925 |
rs74019031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC1 | GRCh38.p7 | 15:63813439 | TGTTTACAAAATCTG[A/G]GTTACTTATCTTTTA | 8925 |
rs74019032 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | HERC1 | GRCh38.p7 | 15:63815195 | CTGATTGTCTAAAAG[C/T]TAAATATGTCCGTTC | 8925 |
rs74019033 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63815472 | AGAAGGTTGTGTAAA[C/G]TAATGAAAACCGTGC | 8925 |
rs74019034 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63819220 | AGTTCATTTCTGGTT[C/G]CATCATTAAAAAAAG | 8925 |
rs74019036 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | HERC1 | GRCh38.p7 | 15:63820807 | ATAGGCATGCCACCA[C/T]GCCCAGCTTAACAGA | 8925 |
rs74019039 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | HERC1 | GRCh38.p7 | 15:63822167 | CTGGCCCGGTCAGGG[A/C]ATACGGATAGTTCAA | 8925 |
rs74019043 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | HERC1 | GRCh38.p7 | 15:63823357 | GGAACTAAATAAATA[C/T]AGATGTAGAAGATTT | 8925 |
rs74019048 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63829025 | CTATATCATGAAAGC[C/T]AGGTTTCTGACAGAG | 8925 |
rs74019049 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63830840 | TTAATTTAGAGAGCC[C/G]GGTAGGCAACATCAG | 8925 |
rs74019051 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | HERC1 | GRCh38.p7 | 15:63832013 | ATTCATAAAAGTTTA[C/G]AATTACAAGAGGCCT | 8925 |
rs74019054 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | HERC1 | GRCh38.p7 | 15:63832868 | ACAATAAAATGTTAA[C/T]CATGAAATGCCACCT | 8925 |
rs74020811 | snp | A/G | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63637017 | GGTGCTCTCTTTGTA[A/G]GCTTCAGAGTCATTA | 8925 |
rs74020812 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63637814 | ACTCCTTGATGACTA[C/T]AAAACTGCTTATTTA | 8925 |
rs74020813 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63638166 | GAAATACATACTGGG[A/C]AGGCCTAACACATCA | 8925 |
rs74020816 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | HERC1 | GRCh38.p7 | 15:63645278 | TAACAACATCACACC[A/C]AGAGATAAGGAGATT | 8925 |
rs74020820 | snp | C/T | 0.201727 | 0.245295 | intron-variant | HERC1 | GRCh38.p7 | 15:63645922 | CTCAACAAATGTTAG[C/T]AGGATAAATGAATTA | 8925 |
rs74021317 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63684189 | GGTGATGTCCCAACA[G/T]GTTAAGCTTTCTAGA | 8925 |
rs74021318 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63684424 | TGTAACTGAAATTTT[C/G]TCCTGGCCAATTCCT | 8925 |
rs74021319 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HERC1 | GRCh38.p7 | 15:63685551 | ACAAAAGCTTAAGAA[C/T]GAAGTCACATGGCTT | 8925 |
rs74021320 | snp | C/T | 0.0137452 | 0.0817538 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63689685 | AGAGAGAAGGGAAAA[C/T]AAGCGCTCAACAATC | 8925 |
rs74021322 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | HERC1 | GRCh38.p7 | 15:63707548 | ATATGACTTAAGCTT[A/G]TGCATAGACTTGACA | 8925 |
rs74021323 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HERC1 | GRCh38.p7 | 15:63710137 | AGAATCTTTGATTTC[C/T]GAGTAGGCAGTGCAG | 8925 |
rs74021324 | snp | C/T | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63710783 | TAGCCATGCAGGCAA[C/T]AGCATTCCAGTCCTA | 8925 |
rs74021325 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63712307 | AGAGGAGAGGACATT[A/G]GAGACACACTAACGG | 8925 |
rs74021327 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | HERC1 | GRCh38.p7 | 15:63718523 | ACCAATTTAGAGCTA[C/G]CTCTCACAGCTTGCA | 8925 |
rs74021328 | snp | C/T | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63721005 | TACAACAAACAGACC[C/T]ATACAACAAGTTTTT | 8925 |
rs74021329 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | HERC1 | GRCh38.p7 | 15:63728053 | GCATATGTATTCTCC[A/G]TACCAACAAATTCAA | 8925 |
rs74021330 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | HERC1 | GRCh38.p7 | 15:63731128 | TGATAAAATATTCCA[C/T]TGAACACATGTACCA | 8925 |
rs74320127 | snp | G/T | 0.0603597 | 0.1629 | intron-variant | HERC1 | GRCh38.p7 | 15:63782903 | CAGACGTGGTGGAAA[G/T]AGCAAGAGAAGTAGA | 8925 |
rs74321359 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | HERC1 | GRCh38.p7 | 15:63746806 | GAAAACAGGAGTAAG[A/G]GAAACAACATCCAAT | 8925 |
rs74334633 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | HERC1 | GRCh38.p7 | 15:63760492 | TCTGAATTACAAACC[C/G]TCAAAAATGAGGTAA | 8925 |
rs74343831 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | HERC1 | GRCh38.p7 | 15:63624024 | CCCACTGTAACCACA[C/T]CAGGTACTAATGTAA | 8925 |
rs74364295 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | HERC1 | GRCh38.p7 | 15:63829336 | GCTGAGGTGGAAGGA[C/T]GGCTTAAGCCCAGGA | 8925 |
rs74432743 | snp | A/C | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63683135 | AGCTACACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 8925 |
rs74436515 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | HERC1 | GRCh38.p7 | 15:63753381 | CCCCCTTTAATGGCT[A/G]TATTTCTAACTTCAA | 8925 |
rs74449517 | snp | C/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63768067 | CAAATCCCTCACTTC[C/T]CAGATAGCTTTCAAT | 8925 |
rs74452506 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | HERC1 | GRCh38.p7 | 15:63665678 | TTTCCTTTTTCAGTA[C/T]AATTTTACACAAAAA | 8925 |
rs74489711 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | HERC1 | GRCh38.p7 | 15:63796142 | ATTCCTAGTTAAATA[C/G]GGAGGAAAATCTTTG | 8925 |
rs74545890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63780447 | AAACAGAAGGCCGGG[C/T]GCGGTGGCTCATACC | 8925 |
rs74564559 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | HERC1 | GRCh38.p7 | 15:63620876 | TCCCTTTATTTTGAG[A/C]CTATATGTGTCTCTG | 8925 |
rs74566370 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | HERC1 | GRCh38.p7 | 15:63662164 | CTAAATAAAAAATTT[C/G]TTTCAAATCAGAATT | 8925 |
rs74605275 | snp | A/T | 0.0670745 | 0.170406 | intron-variant | HERC1 | GRCh38.p7 | 15:63683797 | GGACTGTATAGGCAC[A/T]TGCCCCCATAACTGG | 8925 |
rs74618980 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | HERC1 | GRCh38.p7 | 15:63776937 | AGGGAAGTAAACAGA[C/T]ATCTGTAGTTTATTT | 8925 |
rs74630691 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | HERC1 | GRCh38.p7 | 15:63762749 | TTATTCTGCTCTTCC[C/T]ATATAAACTGTAGCA | 8925 |
rs74635207 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | HERC1 | GRCh38.p7 | 15:63790690 | AACAGGACATCAACT[G/T]TGTGTGTTATGTTTC | 8925 |
rs74639552 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HERC1 | GRCh38.p7 | 15:63722697 | TGGCCCCAAAATGCA[A/G]GAGTAGTGATTCAGT | 8925 |
rs74657578 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63829567 | TGTGTGTGTGTATAT[A/G]TATATATATATATAT | 8925 |
rs74666275 | snp | C/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63644509 | TCTTTGTTTTTTTTT[C/T]CTGTTTTTGCTTTTT | 8925 |
rs74672838 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63639683 | TTTTATCTATGTCAC[A/G]GTTTCTAGAGTAGAC | 8925 |
rs74681872 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | HERC1 | GRCh38.p7 | 15:63733903 | ATAGTGGTCTCATGC[C/T]TATAATCCCAGCACT | 8925 |
rs74686209 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HERC1 | GRCh38.p7 | 15:63717906 | TAGTTTCAATCTTCA[C/T]TTCCAATGGTAGACA | 8925 |
rs74688285 | snp | C/G/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63820695 | TTATCCTTTTTTTTT[C/G/T]GCTTTTGAGACAAGG | 8925 |
rs74692183 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HERC1 | GRCh38.p7 | 15:63712048 | TTTTATATAAATTAG[C/T]ATCTTATTTATCTTT | 8925 |
rs74725659 | snp | C/T | 0.00464811 | 0.0479839 | intron-variant | HERC1 | GRCh38.p7 | 15:63637124 | ACTCTGATGAAGATG[C/T]CCTTTAAAGTCTTTA | 8925 |
rs74755758 | snp | A/C | | | intron-variant | HERC1 | GRCh38.p7 | 15:63808993 | TCATTCTTATGGCCT[A/C]CCTAAAATAAAAAAT | 8925 |
rs74776045 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | HERC1 | GRCh38.p7 | 15:63801825 | TCTTCATGTACATAC[A/C]TTTTTGGATCCCAGC | 8925 |
rs74802579 | in-del | -/TTT | | | intron-variant | HERC1 | GRCh38.p7 | 15:63650429 | AACCTTTTTTTTTTT[-/TTT]GAAAGAGGGTCTTGC | 8925 |
rs74808141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC1 | GRCh38.p7 | 15:63787762 | TCTCTTTTTAAAAAA[C/T]TTACTAACCTGGACA | 8925 |
rs74814914 | snp | C/G | 0.0556399 | 0.157239 | missense | HERC1 | GRCh38.p7 | 15:63696201 | CAAAACACCCTGCTA[C/G]GAACTGCAGCCTCAC | 8925 |
rs74817108 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | HERC1 | GRCh38.p7 | 15:63660734 | TGAAAAAAAAATACA[C/T]CTAATAGAAATTAAT | 8925 |
rs74877824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC1 | GRCh38.p7 | 15:63715444 | AAATACAATTATTTT[C/T]CTTCCCCATCTCCAA | 8925 |
rs74904032 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | HERC1 | GRCh38.p7 | 15:63765134 | TCATAGGTAACTACT[C/T]TCTGTTCACCTTATC | 8925 |
rs74913527 | snp | A/C | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63784065 | GGAAGACTCTATCTC[A/C]AAAAAAAAAAAAAAG | 8925 |
rs74983354 | snp | G/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63806166 | GCAGAACACAAGTGG[G/T]TTTTTTTTTTTCTCT | 8925 |
rs74988373 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | HERC1 | GRCh38.p7 | 15:63753308 | TTTCAAGCAATTAAA[A/G]TCAAGCAATTTAAAA | 8925 |
rs74989953 | snp | A/T | 0.261608 | 0.24973 | intron-variant | HERC1 | GRCh38.p7 | 15:63739386 | TATTTTTAGTAAAAA[A/T]GGGTTTTACCATGTT | 8925 |
rs74994104 | snp | C/T | 0.029116 | 0.117091 | intron-variant | HERC1 | GRCh38.p7 | 15:63782679 | TTTGTAAGGCTATAG[C/T]TGCCACAGATAGTGA | 8925 |
rs74999519 | snp | G/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63675920 | TTTTTTTTTTTTTTT[G/T]GGAGACGGAGTCTTG | 8925 |
rs75000306 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | HERC1 | GRCh38.p7 | 15:63631978 | TAACTACTATCATTA[G/T]GCAGCTAATGTCCTA | 8925 |
rs75025008 | snp | C/T | | | missense | HERC1 | GRCh38.p7 | 15:63764121 | AGACATAATGCTGCC[C/T]CGTAAAGGGAGCACA | 8925 |
rs75031834 | snp | G/T | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63622346 | TTTTTTTTTTTTTTT[G/T]AGATGTGGTCTCGCT | 8925 |
rs75043732 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | HERC1 | GRCh38.p7 | 15:63686822 | TAAAAGTGTGTCTAA[C/T]CATGCTTGAGAAGGA | 8925 |
rs75053664 | snp | A/C | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63772123 | GCAAAACTCCATCTC[A/C]AAAAAAAAAAGGGAA | 8925 |
rs75053830 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HERC1 | GRCh38.p7 | 15:63684495 | AAACTCTTCCTCTTG[C/T]ATCCAACCCTTCTGG | 8925 |
rs75055604 | snp | A/G | 0.0110811 | 0.0736054 | synonymous-codon | HERC1 | GRCh38.p7 | 15:63616496 | GTTGAGAGTCTGCAC[A/G]TAGAGCAGATCCACC | 8925 |
rs75057128 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | HERC1 | GRCh38.p7 | 15:63779122 | AATAATTAGAAAAAG[A/G]TAAGAAAAAAGAATA | 8925 |
rs75081493 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HERC1 | GRCh38.p7 | 15:63786620 | TTTGAGCCTTGTAAA[C/T]ATTCTGCCAATTGAA | 8925 |
rs75095705 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | HERC1 | GRCh38.p7 | 15:63794704 | CTGGGACTCTAGCAG[A/G]AGATGCCACTCTTTC | 8925 |
rs75099135 | snp | C/G | 0.5 | 0 | missense | HERC1 | GRCh38.p7 | 15:63756608 | CTTTTTAATGGATCT[C/G]TGAGGCTCGAATGTT | 8925 |
rs75099547 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | HERC1 | GRCh38.p7 | 15:63803423 | TATCATGCTCTTTTT[C/T]TCTCTCTTTTTTTTT | 8925 |
rs75179657 | snp | G/T | | | intron-variant | HERC1 | GRCh38.p7 | 15:63801008 | ACCAAGCCTACGTAA[G/T]GCAGCTTCCATAAAA | 8925 |
rs75227774 | snp | A/C | 0.444444 | 0.157135 | intron-variant | HERC1 | GRCh38.p7 | 15:63646022 | TGACTAATAATCATT[A/C]CAGTATAAAAAAGAA | 8925 |
rs75229626 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | HERC1 | GRCh38.p7 | 15:63712714 | TTACTCTAACCAAAG[A/C]CTTACATATCATATA | 8925 |
rs75260658 | snp | A/C | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63618173 | aatccatcttgaatt[A/C]atttttgtataaggt | 8925 |
rs75291554 | snp | A/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63730307 | AAAAATTTTTTTTTT[A/T]AATTAGCTGAGCATG | 8925 |
rs75298594 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC1 | GRCh38.p7 | 15:63654476 | TTGGCACTTTTGCAA[A/G]CAATTATTTCACTAA | 8925 |
rs75310661 | snp | A/G | 0 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63829569 | TGTGTGTGTATATAT[A/G]TATATATATATATAT | 8925 |
rs75316361 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | HERC1 | GRCh38.p7 | 15:63738965 | GGATATGTCCCTCTA[A/C]TTGAAAAGTCAGTTT | 8925 |
rs75323682 | snp | A/C | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63711315 | GTAATATCCTGTCTC[A/C]AAAAAAAGGGAAATT | 8925 |
rs75353741 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | HERC1 | GRCh38.p7 | 15:63822600 | CAAAAAAAAAAAAAT[A/T]TTTAAATAATAATTG | 8925 |
rs75359430 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | HERC1 | GRCh38.p7 | 15:63802180 | CCACATGTACTTCTA[A/G]AAGGCTTCATTCAGC | 8925 |
rs75374111 | snp | C/G | 0.079617 | 0.182947 | intron-variant | HERC1 | GRCh38.p7 | 15:63811507 | GCACAGCTGAGCCCC[C/G]GTAACATAAAAGATG | 8925 |
rs75392346 | snp | G/T | 0.5 | 0 | intron-variant | HERC1 | GRCh38.p7 | 15:63622345 | TTTTTTTTTTTTTTT[G/T]GAGATGTGGTCTCGC | 8925 |
rs75398264 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HERC1 | GRCh38.p7 | 15:63688937 | CATTTAAGTTTGGAA[A/G]GCACTGCAGAGTGAT | 8925 |
rs75407582 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC1 | GRCh38.p7 | 15:63722958 | ATGTATTATATAAAT[C/T]TCAATTTTCACACAG | 8925 |
rs75412368 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HERC1 | GRCh38.p7 | 15:63778320 | GATTAAATCCACACC[A/G]TATCTGAAAACACTG | 8925 |