SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs295735 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28234820 | TATCCAGGCAGGGAA[C/T]AGCACATCTGAAGGG | 8924 |
rs295746 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28229813 | TGAGTACTGTTACAG[A/G]TGTTCACAAATACAA | 8924 |
rs295757 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28217086 | gtgtgcgattgagtg[C/T]GAGCATTTGTGTAAA | 8924 |
rs415423 | snp | C/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28205502 | CAGCTCGTTCTAGGA[C/T]TGGGGGAGGCCTCCC | 8924 |
rs916976 | snp | C/T | 0.185472 | 0.241529 | intron-variant | HERC2 | GRCh38.p7 | 15:28268367 | CCAGGTGTTTTCCAA[C/T]TGCCCTGACATGTAG | 8924 |
rs916977 | snp | A/G | 0.47517 | 0.10862 | intron-variant | HERC2 | GRCh38.p7 | 15:28268218 | CTTGGCCAGCCTTCT[A/G]TCTACTCAAACTGCA | 8924 |
rs1129038 | snp | A/G | 0.499894 | 0.00729588 | utr-variant-3-prime | HERC2 | GRCh38.p7 | 15:28111713 | GCCAGGCAGCAGAGC[A/G]CTCGCTGCTGTGTAG | 8924 |
rs1133496 | snp | C/T | 0.0484235 | 0.147875 | synonymous-codon | HERC2 | GRCh38.p7 | 15:28144734 | GTGGAAGTTCATCAG[C/T]GATGGGTCTGTGAAT | 8924 |
rs1614575 | snp | C/T | 0.496937 | 0.0390173 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28317852 | CAGTATGCGCAAATA[C/T]ACAGTGACCTCTCTA | 8924 |
rs1615773 | snp | A/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28298036 | GTGTGTGTGTGTGTG[A/T]GTGAATATTTTCAAA | 8924 |
rs1635160 | snp | A/G | 0.117886 | 0.21224 | intron-variant | LOC107987422, HERC2 | GRCh38.p7 | 15:28315863 | CAAGCTCTAGACAGT[A/G]GCATGCAGTCCCACA | 8924 |
rs1635161 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28313449 | TGGGTGCGGTGGCTC[A/C]CGCCTGTAATCCCAG | 8924 |
rs1635162 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28312880 | TTACTTGCCATGTCA[C/T]TTCAGAGGTGTAAGA | 8924 |
rs1635163 | snp | C/T | 0.126909 | 0.217598 | intron-variant | HERC2 | GRCh38.p7 | 15:28310596 | CTGAACCCCAGTGCA[C/T]GTATTCACTGCCCTC | 8924 |
rs1635165 | snp | C/T | 0.119281 | 0.213102 | intron-variant | HERC2 | GRCh38.p7 | 15:28298942 | CTTGGTTGAGAACCA[C/T]TGTTGAAGTTCGTTG | 8924 |
rs1635166 | snp | A/G | 0.492237 | 0.0618148 | intron-variant | HERC2 | GRCh38.p7 | 15:28294688 | gtaagaacagggtga[A/G]gtgaccttgcttccc | 8924 |
rs1635167 | snp | A/G | 0.119281 | 0.213102 | intron-variant | HERC2 | GRCh38.p7 | 15:28290529 | acataataagaatgt[A/G]gctgtgtgtggtggc | 8924 |
rs1635168 | snp | G/T | 0.466721 | 0.124627 | intron-variant | HERC2 | GRCh38.p7 | 15:28290120 | CTTACCCGTACCTGA[G/T]TATTTAGTAACTTTA | 8924 |
rs1635169 | snp | A/G | 0.118235 | 0.212457 | intron-variant | HERC2 | GRCh38.p7 | 15:28287269 | GTGGAATTTGTAGCT[A/G]TTAGAATAGCTCCTA | 8924 |
rs1635170 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HERC2 | GRCh38.p7 | 15:28287042 | TTTTACAGCGCGCAC[C/G]CACATATTCACCACC | 8924 |
rs1635173 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28250942 | AAAAAATACAAAATA[A/G]AAAGAATAGACACAA | 8924 |
rs1667389 | snp | A/G | 0.118235 | 0.212457 | intron-variant | HERC2 | GRCh38.p7 | 15:28297829 | TTTCAGGTAAAATTT[A/G]TATATAATGAAATGT | 8924 |
rs1667390 | snp | A/G | 0.492287 | 0.0616198 | intron-variant | HERC2 | GRCh38.p7 | 15:28292555 | TTGCTGAGATTTCAG[A/G]TGTGAGCCATCGCAC | 8924 |
rs1667391 | snp | C/T | 0.482083 | 0.0929373 | intron-variant | HERC2 | GRCh38.p7 | 15:28289072 | tttcacttgtcactg[C/T]ccactctcaaatggt | 8924 |
rs1667392 | snp | C/G | 0.294631 | 0.247399 | intron-variant | HERC2 | GRCh38.p7 | 15:28288419 | tctggctcagcctcc[C/G]gagtagctgggatta | 8924 |
rs1667393 | snp | A/G | 0.118584 | 0.212673 | intron-variant | HERC2 | GRCh38.p7 | 15:28287493 | CCTACAGTTATGGGT[A/G]GGTAACTAGACCCGA | 8924 |
rs1667394 | snp | A/G | 0.471004 | 0.116864 | HERC2 | 15 | allele_origin=G(germline)/A(germline) | 15:28285036 | ctttgtttgtttggt[A/G]tatgcacgttttgaa | 8924 |
rs1667395 | snp | A/G | 0.100588 | 0.200439 | intron-variant | HERC2 | GRCh38.p7 | 15:28282892 | ccaggctggagtgca[A/G]tggacgttctcggct | 8924 |
rs1667396 | snp | A/G | 0.121369 | 0.214369 | intron-variant | HERC2 | GRCh38.p7 | 15:28304768 | acattgcgcaggtta[A/G]ttacatatgtataca | 8924 |
rs1667399 | snp | G/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28299147 | GCTTCCAATAAGTGT[G/T]TAATACACCCCCAAA | 8924 |
rs1667400 | snp | A/C | 0.118933 | 0.212888 | intron-variant | HERC2 | GRCh38.p7 | 15:28299213 | AAAATGCCTTCAATT[A/C]ACGTAAAACAATAAA | 8924 |
rs1708965 | snp | C/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28200626 | tccatcaaccaaatg[C/T]agataaggcatacaa | 8924 |
rs1802412 | snp | A/T | | | utr-variant-3-prime | HERC2 | GRCh38.p7 | 15:28111163 | ATGCATTATGTCATC[A/T]GAATTGAGGCCTTTC | 8924 |
rs1802413 | snp | G/T | | | utr-variant-3-prime | HERC2 | GRCh38.p7 | 15:28111249 | TGAATGCATCCAGAG[G/T]ATATTTAAACCAAAA | 8924 |
rs1962780 | snp | A/G | 0.157642 | 0.232314 | intron-variant | HERC2 | GRCh38.p7 | 15:28238397 | TTGTTTTAATACTTG[A/G]AACTCATTTCAAGTT | 8924 |
rs2016236 | snp | A/T | 0.442249 | 0.159814 | intron-variant | HERC2 | GRCh38.p7 | 15:28273423 | GATAGAAATTAGTGT[A/T]GACATTTTGCCTCCA | 8924 |
rs2016277 | snp | A/G | 0.440057 | 0.162414 | intron-variant | HERC2 | GRCh38.p7 | 15:28272823 | ACGATTCAGTGAAAC[A/G]CACACAATGCAACAG | 8924 |
rs2107430 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28199289 | tcccttcctttatga[C/T]acaagttgatccagg | 8924 |
rs2107431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28199274 | cacaagttgatccag[C/G]ctcttcctgtatatt | 8924 |
rs2158400 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28199368 | TTTAGGGTGTGATGT[C/T]TCCACTGTTATGTTT | 8924 |
rs2158401 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28199356 | TGTTTCCACTGTTAT[A/G]TTTTTGATGATCAGG | 8924 |
rs2158402 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28198875 | cagacgtgagccacc[A/G]tgcccAGTCAGAATT | 8924 |
rs2238289 | snp | C/T | 0.49998 | 0.00319482 | intron-variant | HERC2 | GRCh38.p7 | 15:28208069 | TGGAAGATTGGAGCC[C/T]GGGAATTGGATTGGC | 8924 |
rs2240201 | snp | C/G | 0.442791 | 0.15916 | intron-variant | HERC2 | GRCh38.p7 | 15:28269134 | CTGAAGATTGACAAA[C/G]TTCTGTTTATTGTAT | 8924 |
rs2240202 | snp | C/T | 0.185816 | 0.24162 | intron-variant | HERC2 | GRCh38.p7 | 15:28265749 | GGACTTAGTAACCGC[C/T]GTCCTATCTGTTTGA | 8924 |
rs2240203 | snp | A/G | 0.443195 | 0.158668 | intron-variant | HERC2 | GRCh38.p7 | 15:28249056 | TGTTTACATTCCTTA[A/G]ACATTGGGAATGTGG | 8924 |
rs2240204 | snp | C/T | 0.260504 | 0.249779 | intron-variant | HERC2 | GRCh38.p7 | 15:28248886 | CGCTTGTTGCAGATA[C/T]ATTGGACACACTTGG | 8924 |
rs2240205 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28248350 | TTAATTTTGTTGCCT[C/T]AATATTTAAATTCTT | 8924 |
rs2240208 | snp | C/T | 0.444444 | 0.157135 | intron-variant | HERC2 | GRCh38.p7 | 15:28210738 | CATGGGTCAGCAAGA[C/T]TGGTGGCACGCAGGT | 8924 |
rs2245029 | snp | A/G | 0.000519494 | 0.0161083 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28299563 | TCTTTAAAAATTGCA[A/G]TGTGAGTGTGAGCAC | 8924 |
rs2263809 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28303732 | gaaaactgtaaaaca[G/T]tgatgcagaaaattg | 8924 |
rs2269900 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28299054 | GTAAGACTATCATTA[G/T]GTTGTTCATAACAGT | 8924 |
rs2345304 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LOC107987422, HERC2 | GRCh38.p7 | 15:28315965 | AAATGCCCATGTTGG[A/T]CCTCTGCCCTGGACC | 8924 |
rs2345305 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28318727 | TTGCTGGATGTAGGG[C/T]CCTAGGCCTGACGTA | 8924 |
rs2345414 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300033 | actcagcctgagtga[C/T]aagagcgagactcgg | 8924 |
rs2346039 | snp | C/G | 0.260504 | 0.249779 | intron-variant | HERC2 | GRCh38.p7 | 15:28293265 | TTGGGAAGCCATGGC[C/G]GGTGGATCACAAGGT | 8924 |
rs2346040 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28294687 | tgggaagcaaggtca[C/T]ctcaccctgttctta | 8924 |
rs2346041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28294699 | tcacctcaccctgtt[C/G]ttactacaaaatgtg | 8924 |
rs2346042 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28296689 | TGAATTACTGATACA[G/T]AAAAAAAAAAAAAAA | 8924 |
rs2346045 | snp | G/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28296700 | CAGCAACCTTTTTTT[G/T]TTTTTTTTTTATGTA | 8924 |
rs2346046 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28294697 | cattttgtagtaaga[A/G]cagggtgaagtgacc | 8924 |
rs2346047 | snp | C/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28294696 | attttgtagtaagaa[C/G]agggtgaagtgacct | 8924 |
rs2346049 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HERC2 | GRCh38.p7 | 15:28294600 | tggggtcgggtttcc[A/G]cgataaggaggttgt | 8924 |
rs2346050 | snp | A/G | 0.444533 | 0.157025 | intron-variant | HERC2 | GRCh38.p7 | 15:28277538 | GACTTAGGGTTGGTG[A/G]ATTAATTGGAATGTA | 8924 |
rs2346051 | snp | C/T | 0.25912 | 0.249834 | intron-variant | HERC2 | GRCh38.p7 | 15:28277456 | TTTTTTTTAGATAAT[C/T]GTGGATTCACATACA | 8924 |
rs2346083 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28237130 | CCTCAGATTGATGAT[G/T]AAATTTATTTTTCCA | 8924 |
rs2346084 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28237127 | CAGATTGATGATGAA[A/G]TTTATTTTTCCAGCC | 8924 |
rs2346085 | snp | A/G/T | 0.00125398 | 0.0250084 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28237078 | CATACCAGATCTGGG[A/G/T]AGTCTCTCTTCACCT | 8924 |
rs2346086 | snp | A/G | 0 | 0 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28237017 | CTTCTCGGATTACAC[A/G]CTTCGTATTTGGCAA | 8924 |
rs2346090 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC2 | GRCh38.p7 | 15:28236596 | tctctttaaaaaaaG[C/T]AGGAGATagccaggc | 8924 |
rs2346091 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | HERC2 | GRCh38.p7 | 15:28236448 | caaaaattagctggg[C/T]gtggtgacgggtgcc | 8924 |
rs2346092 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28236424 | gggtgcctgtaatcc[C/T]agttactcgggaggc | 8924 |
rs2346093 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28236421 | tgcctgtaatcccag[G/T]tactcgggaggctga | 8924 |
rs2346094 | snp | C/T | 0.248188 | 0.249993 | intron-variant | HERC2 | GRCh38.p7 | 15:28236360 | gaggttgcagtgagc[C/T]gagatcgcgccactg | 8924 |
rs2346095 | snp | A/G | 0.248188 | 0.249993 | intron-variant | HERC2 | GRCh38.p7 | 15:28236353 | cagtgagccgagatc[A/G]cgccactgcactcca | 8924 |
rs2346096 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | HERC2 | GRCh38.p7 | 15:28236313 | acaagagcgagactc[C/G]gtctcaaaaGGAGAG | 8924 |
rs2346097 | snp | A/C | 0.021333 | 0.101051 | intron-variant | HERC2 | GRCh38.p7 | 15:28236296 | tctcaaaaGGAGAGG[A/C]GGATTCAACACAGCT | 8924 |
rs2346098 | snp | C/T | 0.040671 | 0.13668 | intron-variant | HERC2 | GRCh38.p7 | 15:28236282 | GCGGATTCAACACAG[C/T]TGATGATGATAAAAA | 8924 |
rs2346099 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28236272 | CACAGCTGATGATGA[C/T]AAAAATAATAATAAT | 8924 |
rs2346100 | snp | A/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28236266 | TGATGATGATAAAAA[A/T]AATAATAATAAGGAT | 8924 |
rs2346101 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | HERC2 | GRCh38.p7 | 15:28236263 | TGATGATAAAAATAA[A/T]AATAATAAGGATAGT | 8924 |
rs2428632 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28215556 | CTGAAGTTCCCTGCC[C/T]TCAGAGTCAGGGGCC | 8924 |
rs2428635 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28207451 | AGCCGTGAGTGAACA[C/T]GAAAGAGAGTGTGTA | 8924 |
rs2428636 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28207416 | aggcatggtggctta[C/T]gcctgtaatcccaac | 8924 |
rs2428637 | snp | C/G | 1.66668e-05 | 0.00288672 | intron-variant | HERC2 | GRCh38.p7 | 15:28196578 | CAGGTGATTTCTGTT[C/G]TGTCCTAGCTTTCAG | 8924 |
rs2428638 | snp | A/G | | | splice-acceptor-variant, intron-variant | HERC2 | GRCh38.p7 | 15:28196571 | TTTCTGTTCTGTCCT[A/G]GCTTTCAGTGCCAAT | 8924 |
rs2428639 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28196538 | AAAAGATATCATTGT[C/T]GACTTTCCCCAGCAG | 8924 |
rs2428640 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28196020 | AAATCAGGATGGGGT[A/G]TCGGGGAAGAATTAG | 8924 |
rs2428641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC2 | GRCh38.p7 | 15:28309503 | ggaaaaagggagagg[C/T]aaatggaaatcacaa | 8924 |
rs2428642 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | HERC2 | GRCh38.p7 | 15:28309477 | cacaaaagagcatag[C/G/T]ggttatatcagacca | 8924 |
rs2428643 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28303779 | atacgtaggaataaa[A/C]ctaacccaagaagtg | 8924 |
rs2428647 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28235354 | GGCAGGGCTGGCGAG[C/T]TCCAGGGCAGAGGGT | 8924 |
rs2428648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC2 | GRCh38.p7 | 15:28235313 | CTGGCAGGTGGGTCC[A/G]ATCCACAGGAGGATC | 8924 |
rs2428649 | snp | A/G | 0.000299847 | 0.0122407 | intron-variant | HERC2 | GRCh38.p7 | 15:28230324 | TGGCTGAATAGAATC[A/G]TAGCATGTAGCACAG | 8924 |
rs2428650 | snp | A/G | 0.172997 | 0.237846 | intron-variant | HERC2 | GRCh38.p7 | 15:28230224 | TGCTTCATGAACTTG[A/G]CTTATGATGTCCTGG | 8924 |
rs2442398 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321611 | GGGGAGAGAGGGAAA[C/G]AGGGAAGAGATGGAG | 8924 |
rs2442400 | snp | A/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28283208 | taaatctacagatct[A/T]aggtaagcaaaccct | 8924 |
rs2442401 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28283337 | gccttaactatcgtg[C/G]attaacaagtcaaat | 8924 |
rs2525893 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28226555 | gagtccaacctgttt[C/T]ttttgatgatctgat | 8924 |
rs2525894 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HERC2 | GRCh38.p7 | 15:28226549 | aacctgttttttttg[A/T]tgatctgattgtttc | 8924 |
rs2525898 | snp | C/T | 0.277778 | 0.248452 | intron-variant | HERC2 | GRCh38.p7 | 15:28221974 | TAGTTATCTTCTGCA[C/T]AGTTCTGTACGATAT | 8924 |
rs2525899 | snp | C/T | 0.375 | 0.216506 | intron-variant | HERC2 | GRCh38.p7 | 15:28221886 | TGGTTCCCGAGCAGC[C/T]GAAGGGAGTGAACAC | 8924 |
rs2525901 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HERC2 | GRCh38.p7 | 15:28218041 | acctgccgaggtacg[A/G]taggggttagggctt | 8924 |
rs2525907 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28217318 | TCCATGAGAGCATGT[A/G]AGTGGGCAGGTGACT | 8924 |
rs2525908 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | HERC2 | GRCh38.p7 | 15:28217272 | GGGAGTGAAAGCGTC[A/G/T]GTGCATtgagccagt | 8924 |
rs2525909 | snp | C/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28216949 | GTATAGGTGTGAGTG[C/T]AAAGTGAGAAAGTGT | 8924 |
rs2525910 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28216899 | GGTGAGTAATCGGTC[A/G]TTACTAGTGTTGAGG | 8924 |
rs2525911 | snp | A/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28216329 | CTGTCTCTACtaaaa[A/T]tacaaaaaaaaaaaa | 8924 |
rs2525913 | snp | C/T | 0.443598 | 0.158176 | intron-variant | HERC2 | GRCh38.p7 | 15:28212148 | CCTCTTCCCTCCTCC[C/T]CTCCATCCCAGGGCC | 8924 |
rs2525916 | snp | C/T | 0.00836101 | 0.064114 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28211074 | GCAGGTCGGGCGCTG[C/T]TCTCCCACCAGGATA | 8924 |
rs2525919 | snp | A/T | 0.302435 | 0.244439 | intron-variant | HERC2 | GRCh38.p7 | 15:28210654 | ctGTATTGTAACAAG[A/T]AGAACCTAAGCTGGT | 8924 |
rs2525920 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28207964 | CCGAGCAGGGACTCC[G/T]AACAGAGCTAGATTG | 8924 |
rs2525921 | snp | G/T | 0.375 | 0.216506 | intron-variant | HERC2 | GRCh38.p7 | 15:28206193 | CCACAGCACTAAATT[G/T]TGAACACTTTTTTTC | 8924 |
rs2525922 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | HERC2 | GRCh38.p7 | 15:28205974 | GCAGCATGGGTTAAA[C/T]GCTCACATCTTCATG | 8924 |
rs2525923 | snp | G/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28204117 | GCTCTGGGTTCTGCC[G/T]CCTCTGGAGAAAGGG | 8924 |
rs2525925 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HERC2 | GRCh38.p7 | 15:28203716 | GGCGGGCTTTCCCTC[A/G]CATTCTGGTTACTCT | 8924 |
rs2525926 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HERC2 | GRCh38.p7 | 15:28203705 | CCTCGCATTCTGGTT[A/G]CTCTGCCAGGCCGGG | 8924 |
rs2525927 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HERC2 | GRCh38.p7 | 15:28203699 | ATTCTGGTTACTCTG[C/G]CAGGCCGGGACCCCA | 8924 |
rs2525931 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28201785 | CTGAGTAAATTATTC[A/G]TAGGATTAATTTGGA | 8924 |
rs2525933 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28198220 | ctgccaaaggccaca[A/G]aggaactcacctgca | 8924 |
rs2525934 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28196980 | GCTCTTATCAAAGGA[C/T]GAAAGAAGTCTTCAT | 8924 |
rs2525935 | snp | A/G | 0.258843 | 0.249844 | intron-variant | HERC2 | GRCh38.p7 | 15:28196931 | ATTCCCTGAGATACC[A/G]AAGGTATTGTATGGA | 8924 |
rs2525936 | snp | A/C | 0.486464 | 0.0811471 | intron-variant | HERC2 | GRCh38.p7 | 15:28196671 | ACTCTTTGTAAAAAA[A/C]AAATAACTACAATGT | 8924 |
rs2525937 | snp | A/G | 0.000659261 | 0.0181438 | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28196484 | AGAAATGGAGTTGGT[A/G]CCCAGTATTCATCCT | 8924 |
rs2525938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC2 | GRCh38.p7 | 15:28196118 | TATTTTAAGGTTCCT[A/G]TGTATACAGTAATTC | 8924 |
rs2525939 | snp | C/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28311151 | ACTGTACTTCCCTGT[C/G]TTGACTTCTACTGTC | 8924 |
rs2525940 | snp | A/T | 0.121717 | 0.214577 | intron-variant | HERC2 | GRCh38.p7 | 15:28311039 | cccaggctggagtgc[A/T]gtggtgcgatctcca | 8924 |
rs2525941 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28310029 | atgtgagtcactcta[C/T]ctggctAGGGCTCAC | 8924 |
rs2525942 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28310023 | gtcactctacctggc[C/T]AGGGCTCACTTTTTG | 8924 |
rs2525946 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28304146 | tggagtctcactctg[G/T]ggcccaggctggaaa | 8924 |
rs2525950 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28301924 | tagtcccagctactc[G/T]ggaggctgaggcagg | 8924 |
rs2525951 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28301891 | aaacccttgaaccca[A/G]aaggcaaaggttgca | 8924 |
rs2525952 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300787 | TACCCAGGCTGGAGC[A/G]CAGTGACATAATCTC | 8924 |
rs2525953 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300550 | cgggtgtgagccacc[A/G]tggccggccTAAAAC | 8924 |
rs2525955 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28299089 | ACAATCTTATTTAGC[G/T]TTGTAGTTTTGCATG | 8924 |
rs2525956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC2 | GRCh38.p7 | 15:28296606 | GTTTATAAATTAAAA[C/T]TTTTCCCAAAGTGTT | 8924 |
rs2525958 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28294231 | ttcaccttttctctc[C/T]tgttAttaacctgtg | 8924 |
rs2525959 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28288779 | ctcactgcaacctcc[C/G]ccacgtgggttcaag | 8924 |
rs2525962 | snp | C/T | | | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321667 | CTCGGCACACCCTGC[C/T]TACCTTGGAAGGAGG | 8924 |
rs2525963 | snp | C/T | | | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321627 | CCCCACctccctctc[C/T]ctccatctcttccct | 8924 |
rs2525964 | snp | C/T | 0.467234 | 0.12373 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321596 | CTTTCCCTCTCTCCC[C/T]TTCTCTCCCCTCCAC | 8924 |
rs2525970 | snp | C/T | | | intron-variant, nc-transcript-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28320178 | gcaatgggtcaagat[C/T]atgccattgcactcc | 8924 |
rs2525972 | snp | A/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28250586 | TAGATCGTTATTTAC[A/T]TGCTGGCGAGGAGCC | 8924 |
rs2525974 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | HERC2 | GRCh38.p7 | 15:28239480 | GTACAATTTGTACAG[C/G]AAGGACATAATCTAA | 8924 |
rs2525975 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28239342 | ATTTTTATGAACTAA[C/T]AGACTTTTATTGATT | 8924 |
rs2525976 | snp | A/G | 0.000733529 | 0.019137 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28238138 | GGAATCCATGCACGC[A/G]TTTTGTGTTGGCCAG | 8924 |
rs2525978 | snp | G/T | 0.16618 | 0.23553 | intron-variant | HERC2 | GRCh38.p7 | 15:28235193 | AGAACGAATGTGGTG[G/T]GTTGTGGAATGCTCC | 8924 |
rs2525979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28235024 | GCAGTTGTAATTAAC[A/G]TTCGCACTGGTTGAT | 8924 |
rs2525980 | snp | C/T | 0.00111027 | 0.0235352 | intron-variant | HERC2 | GRCh38.p7 | 15:28233806 | TTACTTCCAGCTGTT[C/T]CTGTTGCAGGACTTT | 8924 |
rs2525981 | snp | C/T | 0.00267128 | 0.0364486 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28233697 | GAGGTCGGTCGCTTG[C/T]TGTTATGTTGCCTCT | 8924 |
rs2525982 | snp | A/C/G | 8.28389e-05 | 0.00643533 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28233160 | AGATAATTCGAGAAC[A/C/G]AAGGAAAAAGAGAGG | 8924 |
rs2525985 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28231105 | GAAATTCCACATATC[A/G]CAGTGAATTCAGTTG | 8924 |
rs2525987 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28229943 | TAACCAATTTAAACC[C/T]ATGAGCATTATTTAT | 8924 |
rs2525988 | snp | A/C | | | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28229514 | TACTTCCATCTGTGC[A/C]GTATGCGATGTTTTG | 8924 |
rs2525989 | snp | A/T | 0.000148798 | 0.00862421 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28229247 | GTACGCTTGGGCTGT[A/T]CAGAACATTCGAAAT | 8924 |
rs2595840 | snp | A/G | | | | | GRCh38.p7 | 15:28301354 | caggaggccaaggtt[A/G]cagtgggccaagact | 8924 |
rs2595842 | snp | A/G | | | | | GRCh38.p7 | 15:28304149 | ccagcctgggcccca[A/G]agtgagactcccttt | 8924 |
rs2595843 | snp | C/T | | | | | GRCh38.p7 | 15:28309550 | CTGAAGGGATGGTCT[C/T]CAATTTGAAGAAGCA | 8924 |
rs2595844 | snp | C/T | | | | | GRCh38.p7 | 15:28309555 | GGGATGGTCTTCAAT[C/T]TGAAGAAGCAAGCAG | 8924 |
rs2595846 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 15:28320172 | caggctggagtgcaa[C/T]ggcatgatcttgacc | 8924 |
rs2595847 | snp | A/G | 0.482159 | 0.0927485 | | | GRCh38.p7 | 15:28320784 | CCTGACAAGCTTGCA[A/G]TTATCTCATTAAATC | 8924 |
rs2595850 | snp | C/T | | | | | GRCh38.p7 | 15:28321737 | CACAGGAAGCCAAGT[C/T]ACAATGTCATCCCCC | 8924 |
rs2640404 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28297007 | ATCTTTCGTGCGTAT[A/G]CCCGCAAGCAAGTAC | 8924 |
rs2640409 | snp | C/G | 0.0643423 | 0.167425 | intron-variant | HERC2 | GRCh38.p7 | 15:28202273 | GACTCACAGTGGCTG[C/G]TGTGCTGTGTGTGCC | 8924 |
rs2881147 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300117 | CACACACACGTGCAT[A/G]TGCTCTGAAAAGATA | 8924 |
rs2881294 | snp | A/C | 0.439363 | 0.163222 | intron-variant | HERC2 | GRCh38.p7 | 15:28296605 | AAACACTTTGGGAAA[A/C]ATTTTAATTTATAAA | 8924 |
rs2881308 | snp | C/T | | | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28237082 | TCACCATACCAGATC[C/T]GGGGAGTCTCTCTTC | 8924 |
rs2881309 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | HERC2 | GRCh38.p7 | 15:28236333 | actgcactccagcct[G/T]ggtgacaagagcgag | 8924 |
rs2905935 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28218086 | atcaaactgattaca[G/T]ctgcagcgaccctat | 8924 |
rs2905936 | snp | G/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28217360 | GTGTGATGGTGTGTT[G/T]GTAGCATGTGGTTGT | 8924 |
rs2905937 | snp | C/T | 1.80991e-05 | 0.00300819 | intron-variant | HERC2 | GRCh38.p7 | 15:28215807 | GTCTATTTTCCCTCC[C/T]GCAGCTTCTCCAAAC | 8924 |
rs2905938 | snp | A/G | 6.79579e-05 | 0.00582875 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28215739 | CGCTGGGGTTTGTGC[A/G]GAGCATCGCTCTCAC | 8924 |
rs2905939 | snp | C/T | 0.000101482 | 0.00712254 | missense, upstream-variant-2KB, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28215721 | GCATCGCTCTCACGC[C/T]GCAGGTATGCGGCGC | 8924 |
rs2905940 | snp | A/G | 8.45516e-05 | 0.00650143 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28215714 | TCTCACGCCGCAGGT[A/G]TGCGGCGCCCTCAGC | 8924 |
rs2905941 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28208194 | TAAGAGGAGAGGATG[C/T]TATGAAATTAATTTT | 8924 |
rs2905945 | snp | C/T | 0.0379005 | 0.13234 | intron-variant | HERC2 | GRCh38.p7 | 15:28204223 | CTTTGCAGTTTTTAT[C/T]CCTTGATTATAGTCA | 8924 |
rs2905946 | snp | A/G | 0.00230149 | 0.0338445 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28202360 | TGCTTCCGGGAATGC[A/G]TCCAGCTTGCCTGGT | 8924 |
rs2905947 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28313403 | CCTGGATGGTCTCGA[C/T]CTCCTGACCTTGTGA | 8924 |
rs2905950 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28311282 | agaccgagtttcacc[A/G]tgttgctttggctgg | 8924 |
rs2905952 | snp | C/T | 0.118584 | 0.212673 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300002 | gcagtggtgcgatct[C/T]ggctcactgcaacct | 8924 |
rs2905953 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28299625 | ATTGATTTTATTACC[A/G]AATGATCGAATACAT | 8924 |
rs2905954 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28298452 | GAAAGTACATGGGga[C/T]cgggcgtggtggatc | 8924 |
rs2905955 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28298445 | CATGGGGATcgggcg[C/T]ggtggatcatgcctg | 8924 |
rs2905956 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28294158 | gcactgtgggacaca[A/C]agctggatgtcgcag | 8924 |
rs2905959 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28250513 | TTTATAAGTAGTGAA[C/T]CCCATCAGAATTACA | 8924 |
rs2905960 | snp | A/C | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28239874 | tttcagtctttctcc[A/C]aacaacatggctcca | 8924 |
rs2905961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28233090 | GCTTCACCCTGCCAC[A/G]TTGGATCTGTGATTT | 8924 |
rs2920546 | snp | A/G | | | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321298 | AAATTTCTCGTGTAA[A/G]GCTTTTTTTTAGGGT | 8924 |
rs2920547 | snp | A/G | 0 | 0 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321127 | ACTTGAGATCTATTA[A/G]TAGGCAAAATTTTTT | 8924 |
rs2922706 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28311274 | GTTCGAGACCAGCCA[A/G]AGCAACACGGTGAAA | 8924 |
rs2922711 | snp | A/G | | | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321154 | AAGTTTCGTGCACTT[A/G]CAAGAAACTAATTAA | 8924 |
rs3041289 | in-del | -/GAA | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300061 | ggtgttaaaaaaaaa[-/GAA]aaaaaaagaaaagaa | 8924 |
rs3079904 | in-del | -/AAA/AAAAAA | | | intron-variant | HERC2 | GRCh38.p7 | 15:28285819 | AAAAAAAAAAAAAAA[-/AAA/AAAAAA]GACATAAATTACCAA | 8924 |
rs3079935 | in-del | -/GG | | | intron-variant | HERC2 | GRCh38.p7 | 15:28295318 | GTGTGTGGGGGGGGG[-/GG]AGTGGGGGGGAGGCG | 8924 |
rs3080838 | in-del | -/AT | 0.43655 | 0.16643 | intron-variant | HERC2 | GRCh38.p7 | 15:28263602 | TAATTATGCTGATAT[-/AT]GCAGTTGGGAACACA | 8924 |
rs3081945 | in-del | -/TT | | | intron-variant | HERC2 | GRCh38.p7 | 15:28236917 | CAGATTATTTTTTTT[-/TT]GAACTGTAAGTGCCA | 8924 |
rs3081985 | in-del | -/AAAAAAAA | | | intron-variant | HERC2 | GRCh38.p7 | 15:28236303 | gactccgtctcaaaa[-/AAAAAAAA]GGAGAGGCGGATTCA | 8924 |
rs3094833 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28306447 | ttcaacaacacatta[A/G]aaacatcattcatca | 8924 |
rs3094834 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC2 | GRCh38.p7 | 15:28306387 | ccaggatggttcacc[A/G]tatccaaatcaatca | 8924 |
rs3216954 | in-del | -/AGCACTCTGTA | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28299542 | TGCAATGTGAGTGTG[-/AGCACTCTGTA]AGCTTATCTCGTTTA | 8924 |
rs3862441 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28296695 | CCTTTTTTTTTTTTT[G/T]TTTTTATGTATCAGT | 8924 |
rs3862443 | snp | C/T | 0.444533 | 0.157025 | intron-variant | HERC2 | GRCh38.p7 | 15:28236050 | GCACAGAATGTGGAT[C/T]AGCTGTCCTCTCAGG | 8924 |
rs3881393 | snp | C/G | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28318672 | GCCAGGCATATATAT[C/G]TGGTTATTACATATA | 8924 |
rs3881419 | snp | C/G | 8.23703e-05 | 0.00641704 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28237012 | CGGATTACACGCTTC[C/G]TATTTGGCAATGAGC | 8924 |
rs3881420 | snp | A/G | | | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28237101 | CAGCCTGACCAAGAA[A/G]TCGTCACCATACCAG | 8924 |
rs3901525 | snp | C/T | 0.015872 | 0.0876589 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28215373 | AAGACAATTACACTA[C/T]AAATTCTGTGAAGCA | 8924 |
rs3932767 | snp | C/T | 0.236144 | 0.249616 | intron-variant | LOC107987422, HERC2 | GRCh38.p7 | 15:28315903 | TCGGCGATCAGAGGG[C/T]GATGAAGTTCTAGAT | 8924 |
rs3935591 | snp | A/G | 0.493969 | 0.05458 | intron-variant | HERC2 | GRCh38.p7 | 15:28128866 | CCCTGGAAGCTGGGA[A/G]TAGCTCAGCCAGCAA | 8924 |
rs3940272 | snp | A/C | 0.492037 | 0.0625946 | intron-variant | HERC2 | GRCh38.p7 | 15:28223577 | atagctgcccagggg[A/C]tcctgggagatccac | 8924 |
rs3944122 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28198859 | tgcccAGTCAGAATT[A/C]TTTATTAAGAGTAGA | 8924 |
rs3963457 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HERC2 | GRCh38.p7 | 15:28308122 | agcaatctaccgatt[C/G]agtgcaatccctagc | 8924 |
rs4035903 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HERC2 | GRCh38.p7 | 15:28236588 | aaaaaaGTAGGAGAT[A/G]gccaggcagtggctc | 8924 |
rs4035906 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28235188 | GAATGTGGTGGGTTG[G/T]GGAATGCTCCTGAGT | 8924 |
rs4035907 | snp | G/T | | | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28237100 | AGCCTGACCAAGAAA[G/T]CGTCACCATACCAGA | 8924 |
rs4035908 | snp | C/T | | | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28237069 | TCTGGGGAGTCTCTC[C/T]TCACCTCTGATAGAC | 8924 |
rs4035909 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28237006 | ACACGCTTCGTATTT[A/G]GCAATGAGCACACCG | 8924 |
rs4035910 | snp | A/G | 0.000141168 | 0.00840025 | intron-variant | HERC2 | GRCh38.p7 | 15:28236948 | AGTAAGAAAATCTTT[A/G]CTTTTTGCTGATCAG | 8924 |
rs4035911 | snp | A/G | 0.000147338 | 0.00858179 | intron-variant | HERC2 | GRCh38.p7 | 15:28236938 | TCTTTGCTTTTTGCT[A/G]ATCAGCAGATTATTT | 8924 |
rs4035912 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28236935 | TTGCTTTTTGCTGAT[C/T]AGCAGATTATTTTTT | 8924 |
rs4035913 | snp | A/T | 0.000280308 | 0.0118354 | intron-variant | HERC2 | GRCh38.p7 | 15:28236926 | GCTGATCAGCAGATT[A/T]TTTTTTTTGAACTGT | 8924 |
rs4035914 | snp | C/G | 0.0547245 | 0.156101 | intron-variant | HERC2 | GRCh38.p7 | 15:28236851 | cctgtaatcccagca[C/G]tttgggaggttgtgg | 8924 |
rs4035915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28236735 | ccaggcatgttggca[C/T]gtatttgtagtccca | 8924 |
rs4035961 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28307789 | cttcaataaatggtg[C/T]tgggaaaacttgata | 8924 |
rs4035970 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28308089 | aataccaatgacatt[C/T]ttcacagaaacagaa | 8924 |
rs4035971 | snp | A/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28307826 | aaggtaccaagaaca[A/T]acactggggaaaaga | 8924 |
rs4035974 | in-del | -/AAAAAA | | | intron-variant | HERC2 | GRCh38.p7 | 15:28296703 | ATAAAAAAAAAAAAA[-/AAAAAA]GGTTGCTGATTCCTG | 8924 |
rs4073541 | snp | C/T | 0.255503 | 0.249939 | intron-variant | HERC2 | GRCh38.p7 | 15:28193204 | CCAATATATGGAGCC[C/T]TTGTGGGTCTGTTTC | 8924 |
rs4073542 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | HERC2 | GRCh38.p7 | 15:28192962 | ATTGAGATGATTTTA[C/T]GCTGAGTTGCAATCT | 8924 |
rs4073635 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | HERC2 | GRCh38.p7 | 15:28118293 | GAGGAGAGGCAGCCC[C/T]GTGGGCTTCGGGGAG | 8924 |
rs4092027 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28303685 | aaggaaaagatactc[C/T]gtgttcatggattgg | 8924 |
rs4302011 | snp | C/T | 0.055768 | 0.157397 | intron-variant | HERC2 | GRCh38.p7 | 15:28217095 | ATGCTCGCACTCAAT[C/T]GCACACTTACACACT | 8924 |
rs4372669 | snp | C/G | 0.269538 | 0.249235 | intron-variant | HERC2 | GRCh38.p7 | 15:28225069 | ttaactctacatctg[C/G]aagaactaaaaaaTA | 8924 |
rs4392042 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28217237 | actcatgcctccctc[A/G]tgctcaccctcacac | 8924 |
rs4410052 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28313689 | AATACTAAACATCTA[C/T]TGAACGTAGGACAAC | 8924 |
rs4468588 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HERC2 | GRCh38.p7 | 15:28237188 | CAAAAGGACAGCTCT[C/G]TCCTGCAGCTGTAAC | 8924 |
rs4587952 | snp | C/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28217195 | actgggtgtctcatt[C/T]gcacacccagtaatc | 8924 |
rs4778140 | snp | C/T | 0.33693 | 0.2344 | intron-variant | HERC2 | GRCh38.p7 | 15:28131764 | CCACACCACTGTAAA[C/T]TGAGAGAGTGTGAGC | 8924 |
rs4778141 | snp | G/T | 0.330016 | 0.236849 | intron-variant | HERC2 | GRCh38.p7 | 15:28132976 | ACCTAAACTCAAAAG[G/T]TCACCACTTCCTATC | 8924 |
rs4778142 | snp | C/T | 0.334871 | 0.235153 | intron-variant | HERC2 | GRCh38.p7 | 15:28137361 | catttgactgtgcct[C/T]gctttactgtacctc | 8924 |
rs4778242 | snp | C/T | 0.126564 | 0.217402 | downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28110845 | GAAGTCGGAGGAAAC[C/T]CTGAAGGCTCCAGAG | 8924 |
rs4778243 | snp | A/G | 0.20511 | 0.245937 | downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28110984 | ATCTTTACTACTGCT[A/G]TATCAAGAACTAATT | 8924 |
rs4778244 | snp | A/G | 0.326035 | 0.238157 | utr-variant-3-prime | HERC2 | GRCh38.p7 | 15:28111203 | GGGGACACCTGGGAG[A/G]GGGGACACCAAATGG | 8924 |
rs4778245 | snp | C/T | 0.0619715 | 0.164758 | intron-variant | HERC2 | GRCh38.p7 | 15:28112084 | GAGTACGGCTGCAGT[C/T]TACTTTACTGTGCTC | 8924 |
rs4778246 | snp | C/T | 0.130694 | 0.219696 | intron-variant | HERC2 | GRCh38.p7 | 15:28112650 | GACCCGGCAGGTCCA[C/T]TGAGCTTGTTTCTGA | 8924 |
rs4778247 | snp | C/T | 0.12994 | 0.219284 | intron-variant | HERC2 | GRCh38.p7 | 15:28116618 | ATTTTAACTCAAGAG[C/T]AGGCACAGGCCACAG | 8924 |
rs4778248 | snp | A/G | 0.134119 | 0.221521 | intron-variant | HERC2 | GRCh38.p7 | 15:28126580 | atgattgcatttgcc[A/G]caacctggatgggac | 8924 |
rs4778249 | snp | A/T | 0.342358 | 0.232314 | intron-variant | HERC2 | GRCh38.p7 | 15:28135372 | TTTAGTTTGAGAGTA[A/T]TGTAAATGTTGCCTT | 8924 |
rs4778250 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28136813 | GTGTTTACCAACCCC[C/T]ACCCTAGAAAAAGGA | 8924 |
rs4778252 | snp | C/T | 0.134119 | 0.221521 | intron-variant | HERC2 | GRCh38.p7 | 15:28137626 | gacggtgaacttaaa[C/T]gataaatgtgtatgt | 8924 |
rs4932600 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28152303 | ACAAAAGATATACAC[A/G]TGGGTAACAGAAGCT | 8924 |
rs4932601 | snp | C/T | 0.203575 | 0.245652 | intron-variant | HERC2 | GRCh38.p7 | 15:28289400 | AAAAGTGCATGCACC[C/T]TATAACATTCTCAAA | 8924 |
rs4932602 | snp | A/C/T | 0.0944967 | 0.195752 | intron-variant | HERC2 | GRCh38.p7 | 15:28289480 | atgagagatttcaat[A/C/T]ctcctcAGAAGAAAG | 8924 |
rs4932603 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28311141 | AAGAAAGGATGACAG[C/T]AGAAGTCAAGACAGG | 8924 |
rs4932604 | snp | C/T | 0.047971 | 0.147256 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28314041 | AAACCAGCCCAGTTT[C/T]GCATTCTCTCAATTT | 8924 |
rs4932608 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | HERC2 | GRCh38.p7 | 15:28176175 | AACCGTTCCCATAAA[A/T]CTCACCCAAACAGGA | 8924 |
rs4932618 | snp | A/G | 0.127254 | 0.217792 | intron-variant | HERC2 | GRCh38.p7 | 15:28241923 | atggaaacaacccaa[A/G]tgtcatcaactgatg | 8924 |
rs4932620 | snp | C/T | 0.118584 | 0.212673 | intron-variant | HERC2 | GRCh38.p7 | 15:28269135 | TACAATAAACAGAAC[C/T]TTGTCAATCTTCAGA | 8924 |
rs4932625 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301739 | TGTATGTATGTGTAT[A/G]TATATATATATATAT | 8924 |
rs4932629 | snp | G/T | 0.279461 | 0.248258 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321564 | AGAGAGAACAGAAAG[G/T]GGGGAGAGAAGAGCT | 8924 |
rs4932684 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28223202 | AACTTCCCAATGGAT[C/T]TGAAAATAGGAGCGC | 8924 |
rs4932685 | snp | A/G | 0.245061 | 0.249951 | intron-variant | HERC2 | GRCh38.p7 | 15:28236352 | ctggagtgcagtggc[A/G]cgatctcggctcact | 8924 |
rs4932686 | snp | C/T | 0.021333 | 0.101051 | intron-variant | HERC2 | GRCh38.p7 | 15:28236537 | ctcaggtgatccacc[C/T]gcctcagcctcccaa | 8924 |
rs4932689 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HERC2 | GRCh38.p7 | 15:28240742 | ccaaaaacaatccat[C/T]acgtatttggtcata | 8924 |
rs5017991 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301461 | TGATAGGGACTCCTG[A/G]CCAAATTTATAATAA | 8924 |
rs5741739 | in-del | -/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28192931 | GTTTTTGGGTTTCCC[-/T]TTTTTTTTTTCCAAC | 8924 |
rs5811537 | in-del | -/G | 0.32627 | 0.238082 | downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28110824 | CAGACAGATGGGGCT[-/G]GGGAGGAAGTCGGAG | 8924 |
rs5811538 | in-del | -/A | 0.333261 | 0.235728 | utr-variant-3-prime | HERC2 | GRCh38.p7 | 15:28111411 | AAAGAAAGGAGAAAG[-/A]AAAAAAAATCGATTG | 8924 |
rs5811542 | in-del | -/T | 0.330482 | 0.236691 | intron-variant | HERC2 | GRCh38.p7 | 15:28115742 | GTGCCTAAAAGCCTC[-/T]TAACTCTTCACATCC | 8924 |
rs6416602 | snp | C/T | 0.133777 | 0.221342 | intron-variant | HERC2 | GRCh38.p7 | 15:28124829 | TGTTGGGATTACAGG[C/T]GTGAGCCACCACAAC | 8924 |
rs6416603 | snp | A/G | 0.133777 | 0.221342 | intron-variant | HERC2 | GRCh38.p7 | 15:28130726 | AATAATTAGTGCAAC[A/G]TAAAATCATATTCCA | 8924 |
rs6497270 | snp | A/G | 0.330482 | 0.236691 | intron-variant | HERC2 | GRCh38.p7 | 15:28115894 | TGGCTGTGGTGGGAC[A/G]CACAGCCGAGGACAC | 8924 |
rs6497271 | snp | A/G | 0.333952 | 0.235483 | intron-variant | HERC2 | GRCh38.p7 | 15:28120285 | ATGAGCTGTCCAACA[A/G]AGGACAAGAGTTTCG | 8924 |
rs6497272 | snp | A/G | 0.330249 | 0.23677 | intron-variant | HERC2 | GRCh38.p7 | 15:28121044 | CAATGTAACAGCAGC[A/G]GTTATCATCATGCAG | 8924 |
rs6497273 | snp | A/G | 0.162581 | 0.234218 | intron-variant | HERC2 | GRCh38.p7 | 15:28123712 | CACAAGGCCAGGCAG[A/G]CAGAGAAGGACCGCA | 8924 |
rs6497274 | snp | C/T | 0.32955 | 0.237006 | intron-variant | HERC2 | GRCh38.p7 | 15:28124777 | CTGGTCCTGAACTCC[C/T]GAGTTCAAGCAATCC | 8924 |
rs6497277 | snp | A/G | 0.134119 | 0.221521 | intron-variant | HERC2 | GRCh38.p7 | 15:28131078 | AACTTTCCCTATCCC[A/G]CAAGCTGCTCCTCAT | 8924 |
rs6497278 | snp | A/G | 0.134119 | 0.221521 | intron-variant | HERC2 | GRCh38.p7 | 15:28134875 | atggggtttcatcat[A/G]ttgcccaggctagtc | 8924 |
rs6497279 | snp | C/T | 0.134119 | 0.221521 | intron-variant | HERC2 | GRCh38.p7 | 15:28135157 | TCTGTATTTGCAGTT[C/T]TAGTATCACGCACGT | 8924 |
rs6497280 | snp | C/T | 0.340559 | 0.233022 | intron-variant | HERC2 | GRCh38.p7 | 15:28135166 | GCAGTTTTAGTATCA[C/T]GCACGTTACACAAAA | 8924 |
rs6497281 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28136754 | AGTCGCAACAGAGAC[C/T]ATATGGCCCAAAGCT | 8924 |
rs6497282 | snp | C/T | 0.26818 | 0.249338 | intron-variant | HERC2 | GRCh38.p7 | 15:28139115 | gtgtgacatgctttg[C/T]gaagacacttgcttt | 8924 |
rs6497283 | snp | A/G | 0.256061 | 0.249927 | intron-variant | HERC2 | GRCh38.p7 | 15:28173190 | gctagacgtacacct[A/G]ccatatgatccatcc | 8924 |
rs6497284 | snp | C/T | 0.249886 | 0.25 | intron-variant | HERC2 | GRCh38.p7 | 15:28176880 | GAACTTTCCTAGACT[C/T]GAAGCTTATTTTCTC | 8924 |
rs6497285 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28185312 | GTACTTAGAGCACAG[C/G/T]GTGTCTTGGTCAACA | 8924 |
rs6497286 | snp | G/T | 0.25912 | 0.249834 | intron-variant | HERC2 | GRCh38.p7 | 15:28190423 | TTTGAGAGAGAGAGA[G/T]AATTGCTGATCTGTA | 8924 |
rs6497287 | snp | C/T | 0.284733 | 0.247575 | intron-variant | HERC2 | GRCh38.p7 | 15:28195141 | CTAAGGTTTTTGCAT[C/T]GTTTAGGTGGAGAAT | 8924 |
rs6497288 | snp | A/C | 0.256061 | 0.249927 | intron-variant | HERC2 | GRCh38.p7 | 15:28199711 | ACCTAACCCACCCAA[A/C]CCTGCTTGCCTGTTG | 8924 |
rs6497289 | snp | C/T | 0.442249 | 0.159814 | intron-variant | HERC2 | GRCh38.p7 | 15:28207901 | TAAACAAGTGGTGTG[C/T]CTGTGTTCCCATAAA | 8924 |
rs6497291 | snp | C/T | 0.162909 | 0.23434 | intron-variant | HERC2 | GRCh38.p7 | 15:28250707 | AAAAGTCTCTTACGA[C/T]CTTTAGATAAACTAC | 8924 |
rs6497292 | snp | A/G | 0.440746 | 0.161604 | intron-variant | HERC2 | GRCh38.p7 | 15:28251049 | AAAGTCACATGCAGC[A/G]AGGATGAAGACACAG | 8924 |
rs6497293 | snp | C/G | 0.492727 | 0.0598633 | intron-variant | HERC2 | GRCh38.p7 | 15:28251722 | ggagaatcacttgaa[C/G]ccaagaggcagaggt | 8924 |
rs7161787 | snp | A/G | 0.25045 | 0.25 | intron-variant | HERC2 | GRCh38.p7 | 15:28191596 | CCTCCACGCGTTGGT[A/G]TAATCACAACAGCAC | 8924 |
rs7162272 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HERC2 | GRCh38.p7 | 15:28249615 | ACCCACCAAGGTTAT[A/G]ATAGGAAAATAACAC | 8924 |
rs7162368 | snp | C/T | 0.1652 | 0.235179 | intron-variant | HERC2 | GRCh38.p7 | 15:28195602 | tcttatatggtttca[C/T]ctagatgagatgtct | 8924 |
rs7163356 | snp | A/G | 0.160609 | 0.233472 | intron-variant | HERC2 | GRCh38.p7 | 15:28162308 | accgcactccagccc[A/G]ggtgaaggagactgt | 8924 |
rs7163444 | snp | C/T | 0.467704 | 0.122903 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28222100 | GGCAGCCAGTTCTGG[C/T]CCTGAAACAGGGAGC | 8924 |
rs7163496 | snp | C/T | 0.44306 | 0.158832 | intron-variant | HERC2 | GRCh38.p7 | 15:28252256 | GCAGCTCAAACAGCA[C/T]AGTTGCAGGTCAAAC | 8924 |
rs7164058 | snp | A/G | 0.169435 | 0.236663 | intron-variant | HERC2 | GRCh38.p7 | 15:28173711 | gggaggctgaggtgg[A/G]aggatcacttgagcc | 8924 |
rs7165158 | snp | A/G | 0.349072 | 0.229532 | intron-variant | HERC2 | GRCh38.p7 | 15:28152666 | CTCCCCGCTGGGGCC[A/G]GCCCCTGTACCTGGT | 8924 |
rs7165707 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28126351 | gaactaaaagtagat[C/G]taccatttgatccag | 8924 |
rs7165714 | snp | C/G | 0.165853 | 0.235413 | intron-variant | HERC2 | GRCh38.p7 | 15:28253842 | ttgcggacgcctgta[C/G]tcccagctacttggg | 8924 |
rs7166017 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28210882 | TGCTGGGCAGGCCAC[A/G]TGTCTGTCTTGTACA | 8924 |
rs7166222 | snp | A/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28306598 | tacaataagtttgga[A/T]gtattccctcctcct | 8924 |
rs7166407 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HERC2 | GRCh38.p7 | 15:28161160 | TTAAGTACTTTATCG[C/T]TTTGGTGATCATGTA | 8924 |
rs7166814 | snp | C/T | 0.228842 | 0.249103 | intron-variant | HERC2 | GRCh38.p7 | 15:28191450 | GTCTCACTCTAAGAC[C/T]CAGAAACCATGTATC | 8924 |
rs7167075 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28320719 | ATAAAAGTAGATTGG[C/G]TGTAAATAATTGTCT | 8924 |
rs7167160 | snp | A/G | 0.158302 | 0.232576 | intron-variant | HERC2 | GRCh38.p7 | 15:28137882 | aatgctaggcctctt[A/G]caccagttacccaag | 8924 |
rs7167907 | snp | C/T | 0.16028 | 0.233346 | intron-variant | HERC2 | GRCh38.p7 | 15:28190165 | aggtgcctgccacta[C/T]gcccggctaattttt | 8924 |
rs7169067 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HERC2 | GRCh38.p7 | 15:28237779 | GAATTACACTTCTAC[A/G]TAGTTCTTCCCAAAA | 8924 |
rs7169133 | snp | C/T | 0.329783 | 0.236927 | intron-variant | HERC2 | GRCh38.p7 | 15:28124601 | GTCTCACTCTGTCAC[C/T]CAAGTAAGAGGGCAG | 8924 |
rs7169925 | snp | C/T | 0.165527 | 0.235296 | intron-variant | HERC2 | GRCh38.p7 | 15:28195592 | aaaggataaatctta[C/T]atggtttcacctaga | 8924 |
rs7170607 | snp | G/T | 0.0490175 | 0.148681 | intron-variant | HERC2 | GRCh38.p7 | 15:28216319 | CACTTAAATATTTTT[G/T]TTTTTTGTATTTTTA | 8924 |
rs7170852 | snp | A/T | 0.492137 | 0.0622048 | intron-variant | HERC2 | GRCh38.p7 | 15:28182840 | AATCATTCCAAGCCA[A/T]GGAAACAGACGCACA | 8924 |
rs7170867 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | HERC2 | GRCh38.p7 | 15:28260219 | AAAGAAAAGTaaaaa[C/G]catcatgtaatacac | 8924 |
rs7171058 | snp | A/G | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28200135 | ggcatggtggctcac[A/G]cctataatcccagca | 8924 |
rs7171281 | snp | A/G | 0.166506 | 0.235645 | intron-variant | HERC2 | GRCh38.p7 | 15:28195633 | ggagtggtcatattc[A/G]tagagaccaaagtta | 8924 |
rs7172929 | snp | A/G | 0.245916 | 0.249967 | intron-variant | HERC2 | GRCh38.p7 | 15:28160217 | tctgtccattctcag[A/G]tctcaaactccgttc | 8924 |
rs7173814 | snp | C/T | 0.161267 | 0.233723 | intron-variant | HERC2 | GRCh38.p7 | 15:28210166 | tgagacagagtcttg[C/T]tctgtcgtccaggct | 8924 |
rs7174049 | snp | C/T | 0.00184477 | 0.0303147 | intron-variant | HERC2 | GRCh38.p7 | 15:28191090 | AGAATCAAACAAAGG[C/T]GTCTTTATTATAGAA | 8924 |
rs7176260 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HERC2 | GRCh38.p7 | 15:28181423 | TGAAACACAAATGCA[A/G]TTCAAGACTGCTCCA | 8924 |
rs7176930 | snp | C/T | 0.258288 | 0.249863 | intron-variant | HERC2 | GRCh38.p7 | 15:28195599 | aaatcttatatggtt[C/T]cacctagatgagatg | 8924 |
rs7177047 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | HERC2 | GRCh38.p7 | 15:28166021 | ctggaattttgtgtt[A/G]tgccaaaaagtaagg | 8924 |
rs7178333 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HERC2 | GRCh38.p7 | 15:28261954 | GAACTACAGCCCCCA[C/T]ACACAACGCAGCCCA | 8924 |
rs7179230 | snp | A/G | 0.0486741 | 0.148216 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28314042 | AACCAGCCCAGTTTC[A/G]CATTCTCTCAATTTC | 8924 |
rs7179997 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HERC2 | GRCh38.p7 | 15:28164251 | TGCAACTCTTTCCAC[A/G]AACATAAACAGGCTG | 8924 |
rs7180054 | snp | C/T | 0.133777 | 0.221342 | intron-variant | HERC2 | GRCh38.p7 | 15:28115996 | AGTCTCAGATAAACA[C/T]TGAAGATGCAGAAAC | 8924 |
rs7180269 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HERC2 | GRCh38.p7 | 15:28157178 | aggatttttgcatca[A/G]tgttcatcagggata | 8924 |
rs7180370 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HERC2 | GRCh38.p7 | 15:28164464 | GAACATAACTCACTG[A/G]AGGACAGCAAAAGCA | 8924 |
rs7180372 | snp | C/T | 0.256061 | 0.249927 | intron-variant | HERC2 | GRCh38.p7 | 15:28199907 | GGACATGGTTTCAGC[C/T]ACAAATAAACAGCAT | 8924 |
rs7180381 | snp | C/T | 0.157642 | 0.232314 | intron-variant | HERC2 | GRCh38.p7 | 15:28249804 | aggcacacgccacca[C/T]gccaagctaactttt | 8924 |
rs7180735 | snp | A/G | 0.158962 | 0.232835 | intron-variant | HERC2 | GRCh38.p7 | 15:28165854 | atgttacacacacac[A/G]tattcattctctagc | 8924 |
rs7180762 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HERC2 | GRCh38.p7 | 15:28250011 | CAGGACATGGGAACA[C/T]GGAGGGGAGGAGAGC | 8924 |
rs7180935 | snp | C/T | 0.255503 | 0.249939 | intron-variant | HERC2 | GRCh38.p7 | 15:28170704 | ttctatgaaaggaaa[C/T]gaaaagacaagctag | 8924 |
rs7182309 | snp | A/G | 0.159292 | 0.232964 | intron-variant | HERC2 | GRCh38.p7 | 15:28195437 | CTGCAGTCCAGCCTG[A/G]GCGACAGACTGAGAC | 8924 |
rs7183877 | snp | A/C | 0.285519 | 0.247464 | intron-variant | HERC2 | GRCh38.p7 | 15:28120587 | ACATTTAGAAATGGT[A/C]TACTTGTCGTTTCTT | 8924 |
rs7183945 | snp | A/G | 0.444444 | 0.157135 | intron-variant | HERC2 | GRCh38.p7 | 15:28210771 | GCACACTTTAAATGG[A/G]AAGGCATGAAAATAC | 8924 |
rs7402161 | snp | C/G/T | 0.427911 | 0.175741 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321484 | AAGTAAACACATACG[C/G/T]TGAAGACCTAACGCT | 8924 |
rs7402871 | snp | A/G | | | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28321538 | CCCGAAAGCCAgaaa[A/G]gaaaaaagagagaga | 8924 |
rs7402990 | snp | A/G | 0.264084 | 0.249603 | intron-variant | HERC2 | GRCh38.p7 | 15:28139345 | gcctcccttgctctc[A/G]ctgacagagtcagct | 8924 |
rs7403279 | snp | C/T | 0.482757 | 0.0912364 | intron-variant | HERC2 | GRCh38.p7 | 15:28138419 | tattagttgaattca[C/T]tgaagtcaatgctca | 8924 |
rs7403363 | snp | C/T | 0.272511 | 0.248984 | intron-variant | HERC2 | GRCh38.p7 | 15:28144362 | CAGCTGGTGTGCCCA[C/T]GCATGCCACTGCGAG | 8924 |
rs7403383 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HERC2 | GRCh38.p7 | 15:28147568 | gcttgagcccagagt[C/T]tggggctgtagtgag | 8924 |
rs7494786 | snp | C/T | 0.0906305 | 0.192617 | synonymous-codon | HERC2 | GRCh38.p7 | 15:28169519 | TGCTGTAAGAATATG[C/T]GATAAGGCCTGCTGT | 8924 |
rs7494942 | snp | A/G | 0.474 | 0.111014 | intron-variant | HERC2 | GRCh38.p7 | 15:28118913 | CCGTGGCTGAGCCAG[A/G]GCAGCCCCCAGACGT | 8924 |
rs7495114 | snp | A/G | 0.26271 | 0.249677 | intron-variant | HERC2 | GRCh38.p7 | 15:28171154 | agaacttattttcac[A/G]taaagtaaattttca | 8924 |
rs7495220 | snp | C/T | 3.29484e-05 | 0.00405871 | intron-variant | HERC2 | GRCh38.p7 | 15:28141665 | AGCATTTGCCATGGG[C/T]AAGAACAATGCACAC | 8924 |
rs7495390 | snp | C/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28112136 | AAACCATATTTTTTG[C/G]TAAGAACAAAACAGC | 8924 |
rs7495441 | snp | A/G | 0.134497 | 0.221718 | intron-variant | HERC2 | GRCh38.p7 | 15:28114598 | CAATGCAACAGAGAC[A/G]GATGACCACCAACCT | 8924 |
rs7495442 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28131087 | TATCCCACAAGCTGC[C/T]CCTCATGACCTCTGT | 8924 |
rs7495589 | snp | A/C | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28181493 | TCAAATGAATGAGTT[A/C]TAACTTTATTTCTCA | 8924 |
rs7495599 | snp | C/T | 0.324382 | 0.238678 | intron-variant | HERC2 | GRCh38.p7 | 15:28129773 | ACACAGTATAAGCCT[C/T]TGCCTCCtttttttt | 8924 |
rs7495875 | snp | A/G | 0.170687 | 0.237085 | intron-variant | HERC2 | GRCh38.p7 | 15:28117313 | CAGGCAGACCCTGCC[A/G]TCTGGGGCGCTCGAC | 8924 |
rs7495989 | snp | C/T | 0.32955 | 0.237006 | intron-variant | HERC2 | GRCh38.p7 | 15:28128188 | GAAGTGAAACGATGA[C/T]GCCAGGCACTGAGAG | 8924 |
rs7496200 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28150994 | AGTCAGTAAAACTAA[A/G]ACTTGAAGACTGAAA | 8924 |
rs7496228 | snp | C/G | 0.263535 | 0.249633 | intron-variant | HERC2 | GRCh38.p7 | 15:28151043 | AGCTATTATGCTCTT[C/G]TAGATGCAGTATAAT | 8924 |
rs7496305 | snp | C/T | 0.330016 | 0.236849 | intron-variant | HERC2 | GRCh38.p7 | 15:28127299 | CCCAGGTGCTAGCTC[C/T]GAGGGGAGTCAGCCA | 8924 |
rs7496685 | snp | C/T | 0.00479614 | 0.0487346 | utr-variant-3-prime | HERC2 | GRCh38.p7 | 15:28111350 | TTATAATACGATTTG[C/T]TACACAGTTATTTCC | 8924 |
rs7496724 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | HERC2 | GRCh38.p7 | 15:28119942 | CTAGTTTATCAAAAC[G/T]TCACTGATTCCCAGA | 8924 |
rs7496786 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28273410 | CCACCTTAGAATCTG[A/G]AGGCAAAATGTCAAC | 8924 |
rs7497014 | snp | C/T | 0.133777 | 0.221342 | intron-variant | HERC2 | GRCh38.p7 | 15:28114935 | GAGGCTGCAAGTGCA[C/T]GGCACACACCAAGAT | 8924 |
rs7497403 | snp | A/C | 0.323434 | 0.238972 | intron-variant | HERC2 | GRCh38.p7 | 15:28118043 | TTAAACAGCTTACAG[A/C]GCAGGCTGCCATAAC | 8924 |
rs7497759 | snp | C/T | 0.429538 | 0.173972 | intron-variant | HERC2 | GRCh38.p7 | 15:28171059 | cattctggaaaacgg[C/T]ttggcagtttcttat | 8924 |
rs8023410 | snp | G/T | 0.439918 | 0.162576 | intron-variant | HERC2 | GRCh38.p7 | 15:28298733 | cccgggaggtggagc[G/T]tgcagtgagctgaga | 8924 |
rs8024526 | snp | C/G | 0.272511 | 0.248984 | intron-variant | HERC2 | GRCh38.p7 | 15:28145519 | CAGAAAAACCCACGC[C/G]CACTGGGACCATACC | 8924 |
rs8024600 | snp | A/G | 0.0861689 | 0.188837 | intron-variant | HERC2 | GRCh38.p7 | 15:28198536 | AAATCATTATAATCA[A/G]TATTCATTTAAGGGA | 8924 |
rs8024719 | snp | C/T | 0.168785 | 0.236441 | intron-variant | HERC2 | GRCh38.p7 | 15:28211885 | AATACGCCATAGTTA[C/T]GGGTGAAGCCACACA | 8924 |
rs8025035 | snp | C/T | 0.277209 | 0.248515 | intron-variant | HERC2 | GRCh38.p7 | 15:28132626 | GGAGCATGCAGCCTC[C/T]GGCCTCTGCACACGG | 8924 |
rs8026251 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HERC2 | GRCh38.p7 | 15:28193512 | aatgaaagaagagtc[C/T]ccccaaaaagataga | 8924 |
rs8026590 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC2 | GRCh38.p7 | 15:28199593 | gaaaatcactatggt[A/G]cagcccctaatgata | 8924 |
rs8027732 | snp | A/G | 0.25912 | 0.249834 | intron-variant | HERC2 | GRCh38.p7 | 15:28189404 | CATCCTCTGAACTAT[A/G]TAACTAAGGCACTCT | 8924 |
rs8027911 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HERC2 | GRCh38.p7 | 15:28241425 | tgacaggaacataaa[A/G]tggtgcagccactcc | 8924 |
rs8028689 | snp | C/T | 0.384017 | 0.211044 | intron-variant | HERC2 | GRCh38.p7 | 15:28243742 | tgctaggtcttggca[C/T]ggaagtggaacactg | 8924 |
rs8029149 | snp | C/T | 0.254944 | 0.249951 | intron-variant | HERC2 | GRCh38.p7 | 15:28148928 | CACACAACTCCTAAC[C/T]GAAACATCACCGAGA | 8924 |
rs8029695 | snp | A/G | 0.24134 | 0.24985 | intron-variant | HERC2 | GRCh38.p7 | 15:28179943 | agtgaaaagttcata[A/G]agttacaaataattt | 8924 |
rs8030709 | snp | C/T | 0.44333 | 0.158505 | intron-variant | HERC2 | GRCh38.p7 | 15:28227339 | tctccaaagaagata[C/T]acaaatggccaacaa | 8924 |
rs8030794 | snp | G/T | 0.166506 | 0.235645 | intron-variant | HERC2 | GRCh38.p7 | 15:28216015 | TTCTCAAtttttctt[G/T]ttttttttagagaag | 8924 |
rs8030941 | snp | C/T | 0.431621 | 0.171796 | intron-variant | HERC2 | GRCh38.p7 | 15:28193874 | acatacaaaaataga[C/T]aatttgtaacccaca | 8924 |
rs8031097 | snp | C/T | 0.429238 | 0.174281 | intron-variant | HERC2 | GRCh38.p7 | 15:28193911 | catttttaaaaatat[C/T]aaggggtatcttcag | 8924 |
rs8031458 | snp | C/T | 0.158632 | 0.232706 | intron-variant | HERC2 | GRCh38.p7 | 15:28133927 | gtagtgcaaatcttc[C/T]gaccttttcctcatt | 8924 |
rs8032138 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HERC2 | GRCh38.p7 | 15:28175904 | TGTTGTAGGTTTTCA[G/T]ATAAAGAGACTGAAA | 8924 |
rs8032355 | snp | A/G | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28189710 | aatatttgaggtgat[A/G]gatacattatttagc | 8924 |
rs8033286 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HERC2 | GRCh38.p7 | 15:28190210 | ttttttagtagagac[A/G]gggtttaactgtgtt | 8924 |
rs8033755 | snp | A/C | 0.356811 | 0.226034 | intron-variant | HERC2 | GRCh38.p7 | 15:28136400 | ATAAATGAGCCCCAC[A/C]CCCAAAGCCAGCTTC | 8924 |
rs8033795 | snp | A/C | 0.0980852 | 0.198549 | intron-variant | HERC2 | GRCh38.p7 | 15:28136476 | ATGCAGCATGCCTCC[A/C]AGGACTTCCTATAGA | 8924 |
rs8033952 | snp | A/C | 0.439641 | 0.162899 | intron-variant | HERC2 | GRCh38.p7 | 15:28136577 | CAGCCTCAGCACTGA[A/C]AGGGAGACAGAGGCT | 8924 |
rs8034221 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28315499 | ATAGGGTCAAGCAAT[C/T]AAAAGATCCTATTAA | 8924 |
rs8034648 | snp | C/T | 0.13446 | 0.221699 | intron-variant | HERC2 | GRCh38.p7 | 15:28119650 | gtagagatggggttt[C/T]atcacgttgcccagg | 8924 |
rs8034684 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HERC2 | GRCh38.p7 | 15:28227161 | gtgactgtaatccca[C/G]ctactcgggaggctg | 8924 |
rs8034699 | snp | A/G | 0.429837 | 0.173662 | intron-variant | HERC2 | GRCh38.p7 | 15:28172004 | ggcgtgaacccggga[A/G]gcagagcttgcagtg | 8924 |
rs8034808 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300668 | ctctactaaaaatat[A/G]aaaaattagccgggt | 8924 |
rs8035083 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28221578 | TTAGAAGAGACCTGC[A/G]ATGAGGGAAGATGGA | 8924 |
rs8035922 | snp | A/C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28245566 | AAAAAAAAAAATATA[A/C/T]ACACACACACACACA | 8924 |
rs8036159 | snp | A/C | 0.443195 | 0.158668 | intron-variant | HERC2 | GRCh38.p7 | 15:28254757 | CTGATGCTCTCCAGC[A/C]TCCTTCTGTGAAGTC | 8924 |
rs8036249 | snp | A/G | 0.248755 | 0.249997 | intron-variant | HERC2 | GRCh38.p7 | 15:28194439 | gccgggcgtggtggc[A/G]ggcgcctgtagtcgc | 8924 |
rs8036271 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HERC2 | GRCh38.p7 | 15:28194480 | gaggctgaagcggga[A/G]aatggcatgaacccg | 8924 |
rs8036480 | snp | C/T | 0.266708 | 0.249441 | intron-variant | HERC2 | GRCh38.p7 | 15:28254313 | taaataaaTAACATA[C/T]AATACAATACAGCTA | 8924 |
rs8039195 | snp | C/T | 0.492582 | 0.0604491 | intron-variant | HERC2 | GRCh38.p7 | 15:28270938 | CACAATTAACCTTTA[C/T]CCACGCTTTATATTT | 8924 |
rs8039411 | snp | A/G | 0.133777 | 0.221342 | intron-variant | HERC2 | GRCh38.p7 | 15:28133921 | agtcaggtagtgcaa[A/G]tcttccgaccttttc | 8924 |
rs8039560 | snp | C/T | 0.255782 | 0.249933 | intron-variant | HERC2 | GRCh38.p7 | 15:28171947 | gggcgtggtggcagg[C/T]gcctgtggtcccagc | 8924 |
rs8039663 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | HERC2 | GRCh38.p7 | 15:28298840 | Ttcttcagactaatg[C/G]tctcccaactgagct | 8924 |
rs8040177 | snp | C/T | 0.166506 | 0.235645 | intron-variant | HERC2 | GRCh38.p7 | 15:28219774 | GCACTGCGGTGCTTC[C/T]GGAGGCAGCCCCAGC | 8924 |
rs8040689 | snp | C/T | 0.140242 | 0.224618 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28315145 | GCTTTTCCAGAAGGT[C/T]TGCAAGAAGAAACTA | 8924 |
rs8040781 | snp | C/T | 0.097727 | 0.198275 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28318277 | TAACGTATTACTCTT[C/T]ACGAGAGCAGTGAAG | 8924 |
rs8041145 | snp | A/C | 0.134119 | 0.221521 | intron-variant | HERC2 | GRCh38.p7 | 15:28136115 | AGCATATAAACCACA[A/C]GGGAAAAAACACCTT | 8924 |
rs8041209 | snp | G/T | 0.258607 | 0.249852 | intron-variant | HERC2 | GRCh38.p7 | 15:28198512 | GGATAGCCTACAGAT[G/T]TCAATAACAAATCAT | 8924 |
rs8041320 | snp | A/T | 0.103794 | 0.20279 | intron-variant | HERC2 | GRCh38.p7 | 15:28189839 | aaaaTAAAACTTTTT[A/T]AAAAAATGAATGGTT | 8924 |
rs8042159 | snp | A/G | 0.44858 | 0.151875 | intron-variant | HERC2 | GRCh38.p7 | 15:28240287 | gccgggcgtggtggc[A/G]ggcgcctgtagtccc | 8924 |
rs8042429 | snp | A/G | 0.157642 | 0.232314 | intron-variant | HERC2 | GRCh38.p7 | 15:28231799 | ctgacacaGCAACAG[A/G]AATATTAATCACTTA | 8924 |
rs8042619 | snp | A/C | 0.256897 | 0.249905 | intron-variant | HERC2 | GRCh38.p7 | 15:28199534 | ACAaagctttttttc[A/C]cagaagagaattcca | 8924 |
rs8042892 | snp | A/G | 0.00240512 | 0.0345945 | intron-variant | HERC2 | GRCh38.p7 | 15:28144263 | ACTGTAAACATCCCC[A/G]GGTTTCACAAGCTAG | 8924 |
rs8043281 | snp | A/G | 0.243919 | 0.249926 | intron-variant | HERC2 | GRCh38.p7 | 15:28167301 | aaagaattctgcacc[A/G]ttcctgtggtgtctg | 8924 |
rs8043482 | snp | A/C | 0.0196702 | 0.0972017 | intron-variant | HERC2 | GRCh38.p7 | 15:28224149 | tacacacacacacac[A/C]cacacacacacacac | 8924 |
rs8182028 | snp | C/T | 0.262435 | 0.249691 | intron-variant | HERC2 | GRCh38.p7 | 15:28222789 | ACCTGCTTTCCTTGT[C/T]CTGGAACTTCGTATG | 8924 |
rs8182077 | snp | A/G | 0.262159 | 0.249704 | intron-variant | HERC2 | GRCh38.p7 | 15:28222824 | AGGAAGGGGGTGCCC[A/G]TGTGATCAGCCCTAA | 8924 |
rs9302376 | snp | C/T | 0.166832 | 0.235761 | intron-variant | HERC2 | GRCh38.p7 | 15:28261304 | TCATATTCTCCCATC[C/T]GAGATTTAACAATGC | 8924 |
rs9331441 | snp | A/G | 0.0482946 | 0.147699 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28318266 | TCTTAGCTCTGTAAC[A/G]TATTACTCTTTACGA | 8924 |
rs9672907 | snp | C/T | 0.165853 | 0.235413 | intron-variant | HERC2 | GRCh38.p7 | 15:28286114 | aaaaaagaattaaca[C/T]ggactcaaaacaatc | 8924 |
rs9707870 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305755 | caacctacaacatgg[A/G]agaaaattttcgcaa | 8924 |
rs9707873 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305767 | tgggagaaaattttc[A/G]caacctactcatctg | 8924 |
rs9707874 | snp | C/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305798 | ACAAAGGGCTAATAT[C/G]CAGAATCTACAATGA | 8924 |
rs9707939 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305481 | gctagccatatgtag[A/G]aagctgaaactggat | 8924 |
rs9707952 | snp | C/T | 0.330016 | 0.236849 | intron-variant | HERC2 | GRCh38.p7 | 15:28119166 | TTTGGGAGGCCGAGG[C/T]GAGTGGATCACCTGC | 8924 |
rs9707953 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305785 | acctactcatctgac[A/G]aagggctaatatgca | 8924 |
rs9707954 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305828 | aactcaaacaaattt[A/G]caagaaaaaaacaaa | 8924 |
rs9708080 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305795 | ctgacaaagggctaa[C/T]atgcagaatctacaa | 8924 |
rs9708139 | snp | C/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305329 | tagtaccaaaacaga[C/G]atatagatcaatgga | 8924 |
rs9708140 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305338 | aacagacatatagat[C/G]aatggaacagaacag | 8924 |
rs9708243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERC2 | GRCh38.p7 | 15:28305369 | agccctcagaaataa[C/T]gccgcatacctacaa | 8924 |
rs9708257 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305750 | acaggcaacctacaa[A/C]atgggagaaaatttt | 8924 |
rs9744225 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305315 | CACAATGGTTGAACT[A/G]GTACCAAAACAGACA | 8924 |
rs9744526 | snp | A/C | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305694 | ggatctaattaaact[A/C]aagagcttctgcaca | 8924 |
rs9744809 | snp | A/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305393 | cctacaactatctga[A/T]ctttgacaaacctga | 8924 |
rs9745265 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305378 | aaataacgccgcata[C/T]ctacaactatctgat | 8924 |
rs9745296 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305648 | ccaaaacaccaaaag[C/T]aatggcaacaaaagc | 8924 |
rs9806328 | snp | C/T | 0.0792297 | 0.182586 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28178954 | CCGTGGGATGGGCAC[C/T]GTCCCGCTGGAAATG | 8924 |
rs9806503 | snp | G/T | 0.245061 | 0.249951 | intron-variant | HERC2 | GRCh38.p7 | 15:28180625 | AGCTATTCACTCTAT[G/T]TGGGTACATCTGAAC | 8924 |
rs9944196 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305453 | tatttaataaatggt[A/G]ctgggaaaactggct | 8924 |
rs9944287 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305362 | agaacagagccctca[A/G]aaataacgccgcata | 8924 |
rs9972294 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28314631 | GGAGGCCAAGGCGGG[C/T]GGATCATGAGGTCAG | 8924 |
rs9989302 | snp | C/G | 0.135484 | 0.22223 | intron-variant | HERC2 | GRCh38.p7 | 15:28145755 | ATACTTGGTAAAAGA[C/G]CATTTCACAAGCACC | 8924 |
rs9989342 | snp | A/C | 0.158302 | 0.232576 | intron-variant | HERC2 | GRCh38.p7 | 15:28145443 | CTTTCCACTGGATGC[A/C]GAAAAACTCACATCC | 8924 |
rs10083607 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HERC2 | GRCh38.p7 | 15:28275618 | TATGCATATGGTACA[C/T]CATAAAAATCATCCT | 8924 |
rs10083641 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HERC2 | GRCh38.p7 | 15:28275408 | AGGGTAGCCTGGCTC[A/G]CCCCAGCTCCGGCGT | 8924 |
rs10152176 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | HERC2 | GRCh38.p7 | 15:28188238 | actgactgaatatta[C/T]atgacattaaagagt | 8924 |
rs10152659 | snp | A/G | 0.040671 | 0.13668 | intron-variant | HERC2 | GRCh38.p7 | 15:28288219 | AACAAAACCTTAAGG[A/G]CCCATAATGGTAAAA | 8924 |
rs10152818 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | HERC2 | GRCh38.p7 | 15:28259523 | atgccaatattttgt[A/G]taaggtcagctttcc | 8924 |
rs10152874 | snp | A/G | 0.250732 | 0.249999 | intron-variant | HERC2 | GRCh38.p7 | 15:28188258 | cattaaagagtaatt[A/G]ttggctgggcacggt | 8924 |
rs10152883 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | HERC2 | GRCh38.p7 | 15:28259172 | ccatcccggctcact[A/G]caatttctgcctccc | 8924 |
rs10162835 | snp | C/T | 0.255503 | 0.249939 | intron-variant | HERC2 | GRCh38.p7 | 15:28157568 | tgatggtagtttgta[C/T]ttctatggaatcagt | 8924 |
rs10162844 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | HERC2 | GRCh38.p7 | 15:28137989 | tgatatagagaatgt[C/T]tggcatagacagaag | 8924 |
rs10162958 | snp | A/G | 0.3748 | 0.216622 | intron-variant | HERC2 | GRCh38.p7 | 15:28262679 | GAAAGTCAACTCAAC[A/G]GGTTTAAATTACATT | 8924 |
rs10163086 | snp | C/G | 0.241627 | 0.24986 | intron-variant | HERC2 | GRCh38.p7 | 15:28155632 | ttttcttgtaaattt[C/G]tttgagttctttgta | 8924 |
rs10163174 | snp | A/G | 0.093777 | 0.195178 | intron-variant | HERC2 | GRCh38.p7 | 15:28137950 | aaacacacaaatgat[A/G]agaatgcaaaacagt | 8924 |
rs10163184 | snp | A/G | 0.246485 | 0.249975 | intron-variant | HERC2 | GRCh38.p7 | 15:28155215 | attgtgaatagtgcc[A/G]caataaacatatgtg | 8924 |
rs10431853 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305707 | ctaaagagcttctgc[A/G]cagcaaaagaaacta | 8924 |
rs10438451 | snp | A/C | 0.093777 | 0.195178 | intron-variant | HERC2 | GRCh38.p7 | 15:28163427 | GACCTTAAGAAACAG[A/C]TTAAGAAACGACGGC | 8924 |
rs10459717 | snp | G/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305680 | aaaattgacaaatgg[G/T]atctaattaaactaa | 8924 |
rs10468154 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | HERC2, LOC107987422 | GRCh38.p7 | 15:28312250 | GTGAAGCCCAGGAGA[A/G]GAGCTCTCCAGATCA | 8924 |
rs10536211 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301735 | TAGTTGtatgtatgt[A/G]tatatatatatatat | 8924 |
rs10594927 | in-del | -/CA | 0.375 | 0.216506 | intron-variant | HERC2 | GRCh38.p7 | 15:28245672 | ATATACACACACACA[-/CA]TACATAAACACACAT | 8924 |
rs10626153 | in-del | -/AG/AGT/TAG | | | intron-variant | HERC2 | GRCh38.p7 | 15:28289408 | TGCACCTTATAACAT[-/AG/AGT/TAG]TCTCAAATACATGAA | 8924 |
rs10627923 | in-del | -/CT | 0.064029 | 0.167077 | intron-variant | HERC2 | GRCh38.p7 | 15:28132050 | GGGCCCTGGGGGCCC[-/CT]GACTGCGGTGAGCTG | 8924 |
rs10852220 | snp | A/G | 0.224116 | 0.248656 | intron-variant | HERC2 | GRCh38.p7 | 15:28136323 | CAAACGTGCTGCTGC[A/G]CTGACATAATATAAG | 8924 |
rs10852221 | snp | A/C | 0.0773933 | 0.180851 | intron-variant | HERC2 | GRCh38.p7 | 15:28309148 | CAGCCATCAGATGAA[A/C]TGTTCTAGAAATATC | 8924 |
rs11074319 | snp | A/G | 0.330249 | 0.23677 | intron-variant | HERC2 | GRCh38.p7 | 15:28119808 | AATTGCATACTGAAC[A/G]TTTTTGTAACACAAG | 8924 |
rs11074320 | snp | A/G | 0.330249 | 0.23677 | intron-variant | HERC2 | GRCh38.p7 | 15:28122050 | CCATACAGCAGCCAC[A/G]GGGCCAGGGAGCACC | 8924 |
rs11074321 | snp | A/G | 0.330016 | 0.236849 | intron-variant | HERC2 | GRCh38.p7 | 15:28122205 | AAACATCAGCACCAC[A/G]GTGAGGACCCAGCCG | 8924 |
rs11074322 | snp | C/T | 0.329783 | 0.236927 | intron-variant | HERC2 | GRCh38.p7 | 15:28123849 | AACTCCAAAAGGGAA[C/T]AGATTTTTGTCTGTT | 8924 |
rs11074323 | snp | A/C | 0.333491 | 0.235646 | intron-variant | HERC2 | GRCh38.p7 | 15:28125762 | TCACTGCAGCCTCAA[A/C]CTCCCCAGCTCAAGT | 8924 |
rs11074324 | snp | C/T | 0.329783 | 0.236927 | intron-variant | HERC2 | GRCh38.p7 | 15:28125922 | GTTCGAGCGATTCTC[C/T]GGCCTCAGCCTCCTG | 8924 |
rs11074325 | snp | A/G | 0.228547 | 0.249078 | intron-variant | HERC2 | GRCh38.p7 | 15:28136321 | TTCAAACGTGCTGCT[A/G]CACTGACATAATATA | 8924 |
rs11074326 | snp | C/T | 0.422944 | 0.180528 | intron-variant | HERC2 | GRCh38.p7 | 15:28171281 | ATACTGAACATACTA[C/T]GTAATATGTAACAAC | 8924 |
rs11074327 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305474 | AAAACTGGCTAGCCA[C/T]ATGTAGAAAGCTGAA | 8924 |
rs11074328 | snp | A/C | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305558 | ATTTAAACGTTAGAC[A/C]TAAAACCATAAAAAC | 8924 |
rs11074330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC2 | GRCh38.p7 | 15:28305766 | ATGGGAGAAAATTTT[C/T]GCAACCTACTCATCT | 8924 |
rs11268055 | in-del | -/AGGGAGCACGTGCACCGCCCCACGTGC | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28205288 | TCCCAGCATGACTGC[-/AGGGAGCACGTGCACCGCCCCACGTGC]TCTCAAGTTGCTCAG | 8924 |
rs11307271 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301802 | TATATTCTATCTAAC[-/T]TTTTTTTTTTTTTTT | 8924 |
rs11316923 | in-del | -/T | 0.252702 | 0.249985 | intron-variant | HERC2 | GRCh38.p7 | 15:28183393 | TTTTGCATTTTTTTT[-/T]GTAGAGACGGGGTCT | 8924 |
rs11324616 | in-del | -/A | 0.499121 | 0.020948 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28314864 | AGACTCCCTCTCAGG[-/A]AAAAAAAAAAAAAAA | 8924 |
rs11324806 | in-del | -/A | 0.14665 | 0.227637 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28318623 | GTCAGACTCCATCTC[-/A]AAAAAAAAAAAAGTA | 8924 |
rs11340454 | in-del | -/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28249834 | TTTTTTTTTTTTTTT[-/T]AAGTGGAGACGGGCT | 8924 |
rs11356508 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28276193 | tccatctcaaaaaac[A/G]aaaaaaaaaaaaaaa | 8924 |
rs11359639 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28276217 | AAAAAAAAAAAAAAA[-/A]GAGGGTTGTTATAGA | 8924 |
rs11365574 | in-del | -/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28116223 | AGTCTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT | 8924 |
rs11367353 | in-del | -/C | 0.329783 | 0.236927 | intron-variant | HERC2 | GRCh38.p7 | 15:28124566 | GCTGGCATGAACATT[-/C]AAGGTTCTTTTGAGA | 8924 |
rs11375781 | in-del | -/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28115263 | AAATAGATGGTCTAT[-/T]TTTTTTTTTTTTTTT | 8924 |
rs11396433 | in-del | -/A | | | intron-variant | LOC107987422, HERC2 | GRCh38.p7 | 15:28316060 | TAAAAAAAAAAAAAA[-/A]TTATCTGGGTGTGGT | 8924 |
rs11507963 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305864 | CCATCAAAAAGTGGG[C/T]GAAGGACATGAACAG | 8924 |
rs11507964 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305917 | TATGCAGCCAAAAAA[C/T]ACATGAAAAATGCTC | 8924 |
rs11507965 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305981 | AACCACTATGAGATA[C/T]CATCTCACACCAGTT | 8924 |
rs11508649 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305708 | TAAAGAGCTTCTGCA[C/T]AGCAAAAGAAACTAC | 8924 |
rs11508650 | snp | G/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305710 | AAGAGCTTCTGCACA[G/T]CAAAAGAAACTACCA | 8924 |
rs11508652 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28305946 | TCATCATCACTGGCC[A/G]TCAGAGAAATGCAAA | 8924 |
rs11631797 | snp | A/G | 0.429638 | 0.173868 | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28257133 | GGGCCAGTCCGCGGA[A/G]CCATCCATCCCCTCA | 8924 |
rs11633252 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28133152 | TTTAAAAAAAAAAAA[A/G]AAGAATCATATgcaa | 8924 |
rs11635884 | snp | C/T | 0.330016 | 0.236849 | intron-variant | HERC2 | GRCh38.p7 | 15:28123823 | GCATCTTACTGTTTG[C/T]TTTTAATATAAACTC | 8924 |
rs11636232 | snp | C/T | 0.379195 | 0.21403 | synonymous-codon | HERC2 | GRCh38.p7 | 15:28141480 | TTCCCCTCCGATTAA[C/T]TGCACGGGTCTGAGA | 8924 |
rs11638174 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28263990 | caccactgcacacca[G/T]cctgggtgacagagc | 8924 |
rs11638971 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28128747 | TCGCTCTGCAGGTGA[A/G]AAGCCCCGCATGGGT | 8924 |
rs11853181 | snp | A/T | 0.046775 | 0.145601 | intron-variant | HERC2 | GRCh38.p7 | 15:28309056 | aggtttgaattttta[A/T]tgacttattttgtgg | 8924 |
rs11853593 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | HERC2 | GRCh38.p7 | 15:28193566 | atgtgaagaaatact[A/G]aaagacagaattttc | 8924 |
rs11854005 | snp | A/G | 0.0067987 | 0.0579062 | synonymous-codon | HERC2 | GRCh38.p7 | 15:28124177 | GGTGCAGCAGCAGCA[A/G]ACGGTTCCTCAGCGC | 8924 |
rs11855003 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28139936 | agccaggcgtggtgg[C/T]gggcgcctgttgtcc | 8924 |
rs11855331 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | HERC2 | GRCh38.p7 | 15:28137472 | atgtgctgacttacc[A/G]tcgctatgtcacgtt | 8924 |
rs11856014 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HERC2 | GRCh38.p7 | 15:28266281 | accactttgggaggc[C/T]gaggtgggcagatca | 8924 |
rs11856335 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28139913 | aaaaaaaaaaaaaaa[A/G]aaagattagccaggc | 8924 |
rs11856675 | snp | C/T | 0.25045 | 0.25 | intron-variant | HERC2 | GRCh38.p7 | 15:28192295 | AAATGCCACAAATGG[C/T]TTCCCTAGTCAAGAT | 8924 |
rs11857135 | snp | C/T | 0.34437 | 0.231505 | intron-variant | HERC2 | GRCh38.p7 | 15:28139777 | ATCCATTAGAAAACA[C/T]Tggccgggcacggta | 8924 |
rs11857158 | snp | C/G | | | intron-variant, downstream-variant-500B | HERC2, LOC107987422 | GRCh38.p7 | 15:28312541 | GAGGCTACAGCAGGA[C/G]GGTCACCTGCACCCA | 8924 |
rs11858357 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28185611 | TTCTAGATACATGCC[C/T]TGGGAAATGCACAAG | 8924 |
rs12015172 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305484 | agccatatgtagaaa[A/G]ctgaaactggatccc | 8924 |
rs12015174 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305351 | atcaatggaacagaa[C/T]agagccctcagaaat | 8924 |
rs12015175 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305744 | gagtgaacaggcaac[C/G]tacaacatgggagaa | 8924 |
rs12015177 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305682 | aattgacaaatggga[C/T]ctaattaaactaaag | 8924 |
rs12050490 | snp | A/G | 0.371177 | 0.218669 | intron-variant | HERC2 | GRCh38.p7 | 15:28295560 | tgcatcaccatgccc[A/G]gctaattttttgttt | 8924 |
rs12324024 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305425 | aaaaacaagcaatgg[A/G]gaaaggattccctat | 8924 |
rs12324190 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28302001 | gatggggtttcaccg[G/T]gttggccaggatggt | 8924 |
rs12324220 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28303323 | tcactgtagatgtat[A/G]gatctgtttctgggt | 8924 |
rs12324458 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301733 | ACTAGTTGtatgtat[A/G]tgtatatatatatat | 8924 |
rs12385981 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305390 | atacctacaactatc[C/T]gatctttgacaaacc | 8924 |
rs12397537 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305409 | ctttgacaaacctga[C/G]aaaaacaagcaatgg | 8924 |
rs12397548 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305663 | caatggcaacaaaag[A/C]caaaattgacaaatg | 8924 |
rs12397551 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305646 | gtccaaaacaccaaa[A/G]gcaatggcaacaaaa | 8924 |
rs12397552 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305331 | gtaccaaaacagaca[G/T]atagatcaatggaac | 8924 |
rs12397554 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305406 | gatctttgacaaacc[C/T]gagaaaaacaagcaa | 8924 |
rs12397557 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28305343 | acatatagatcaatg[A/G]aacagaacagagccc | 8924 |
rs12438034 | snp | A/G | 0.330249 | 0.23677 | intron-variant | HERC2 | GRCh38.p7 | 15:28125408 | TCCAAAGAGGCGAGT[A/G]TACTTCCCAGGACTC | 8924 |
rs12438302 | snp | A/G | 0.27278 | 0.24896 | intron-variant | HERC2 | GRCh38.p7 | 15:28293470 | TGCACTCCAGCCTGG[A/G]TGACAGAGCGAGACT | 8924 |
rs12439418 | snp | A/T | 0.0317378 | 0.121908 | intron-variant | HERC2 | GRCh38.p7 | 15:28161592 | GAccaattcagcagc[A/T]actagccacatgtgc | 8924 |
rs12440228 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28310884 | AGATAAAGACCATCC[C/T]GGCTAACACAGCGAA | 8924 |
rs12441070 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28292474 | taccgctgcaagaat[A/G]taaaacaatgtagcc | 8924 |
rs12442229 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28310834 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAAGCG | 8924 |
rs12442471 | snp | C/G | 0.00934559 | 0.067716 | intron-variant | HERC2 | GRCh38.p7 | 15:28267957 | CATCACTCCATGGGG[C/G]TGGCAGACCTCCCAA | 8924 |
rs12591531 | snp | A/G | 0.284471 | 0.247612 | intron-variant | HERC2 | GRCh38.p7 | 15:28182770 | TTTTTGGTGGAAAAC[A/G]ATGATACACCAGGCC | 8924 |
rs12591595 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28232526 | tgcactccagcctgg[C/T]gacaaagcaagattc | 8924 |
rs12591834 | snp | A/G | 0.0150935 | 0.0855507 | intron-variant | HERC2 | GRCh38.p7 | 15:28178245 | TGCGTGGGCAGGAGG[A/G]CACACTGTGTGGTGC | 8924 |
rs12592282 | snp | A/G | 0.26271 | 0.249677 | intron-variant | HERC2 | GRCh38.p7 | 15:28184127 | GCCCGGGAGGCAGAG[A/G]TTGCAGTGAGCTGAG | 8924 |
rs12592363 | snp | A/G | 0.260504 | 0.249779 | intron-variant | HERC2 | GRCh38.p7 | 15:28242183 | TGGTGTTTAATAGAT[A/G]CATAGTTTCAGTTGA | 8924 |
rs12592730 | snp | A/G | 0.259674 | 0.249813 | intron-variant | HERC2 | GRCh38.p7 | 15:28285213 | caatcaaaatttaca[A/G]aacactccagccaat | 8924 |
rs12593929 | snp | A/G | 0.463774 | 0.129618 | intron-variant | HERC2 | GRCh38.p7 | 15:28114112 | CCCACCTGCCACACG[A/G]GGCCTCACCCAGACA | 8924 |
rs12595630 | snp | C/T | 0.261884 | 0.249717 | intron-variant | HERC2 | GRCh38.p7 | 15:28241578 | cgtaatcccatcact[C/T]tgggaggccgaggtg | 8924 |
rs12595706 | snp | G/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28154094 | TAAGGTTAAGAGTGG[G/T]GATTATAAACTCTGT | 8924 |
rs12595735 | snp | C/T | 0.282632 | 0.247861 | intron-variant | HERC2 | GRCh38.p7 | 15:28289514 | AACTAAGCAGTGAAA[C/T]TGCTCTTCATGCCTC | 8924 |
rs12898729 | snp | A/G | 0.279726 | 0.248226 | intron-variant | HERC2 | GRCh38.p7 | 15:28147115 | ACTGGGTGAGACCCC[A/G]CGGTGCTCTAGCCCA | 8924 |
rs12898763 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant | HERC2 | GRCh38.p7 | 15:28221916 | AACACCTGTGTCATC[A/C/G]ATCAACTGACACATC | 8924 |
rs12900211 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HERC2 | GRCh38.p7 | 15:28236015 | TGGTAAAAACACAGT[C/G]CTCAAGTAGAATGCT | 8924 |
rs12900486 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214543 | CCCACCTCTGAGTGA[C/T]GGCACTGCGCCGCTC | 8924 |
rs12901047 | snp | A/T | 0.343701 | 0.231776 | intron-variant | HERC2 | GRCh38.p7 | 15:28145780 | AGCACCCAAAGACGG[A/T]CCTGACCTGTCCCAG | 8924 |
rs12902913 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28140338 | AGCTCCCATTCTCCC[A/G]CACAAACGGGAAAAA | 8924 |
rs12903263 | snp | A/G | 0.00479764 | 0.0487422 | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28257130 | CGGGGGCCAGTCCGC[A/G]GAGCCATCCATCCCC | 8924 |
rs12903534 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28199084 | cctggaaggtggagg[C/T]tacaatgagccaaga | 8924 |
rs12904176 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC2 | GRCh38.p7 | 15:28236021 | AAACACAGTCCTCAA[A/G]TAGAATGCTGTTCCC | 8924 |
rs12904181 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HERC2 | GRCh38.p7 | 15:28236031 | CTCAAGTAGAATGCT[C/G]TTCCCTGAGAGGACA | 8924 |
rs12904397 | snp | C/G | 0.281313 | 0.248031 | intron-variant | HERC2 | GRCh38.p7 | 15:28236157 | GGGTAGACGGGTAGA[C/G]ATTCCTGCACACTTT | 8924 |
rs12904474 | snp | G/T | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214518 | AGGGCACAGGGAAGG[G/T]AGACGGCCACCCACC | 8924 |
rs12904487 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214541 | CACCCACCTCTGAGT[A/G/T]ACGGCACTGCGCCGC | 8924 |
rs12906631 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28276147 | gccaagatcgcacct[C/T]tgcactccagcctgg | 8924 |
rs12908005 | snp | G/T | 0.375 | 0.216506 | intron-variant | HERC2 | GRCh38.p7 | 15:28287740 | TTTTTTTTTTTTTTG[G/T]TTTGAGATGGAGTCT | 8924 |
rs12911840 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28160003 | ggaggtccactccca[G/T]actctgtttgcctgg | 8924 |
rs12912427 | snp | A/G | 0.308908 | 0.242961 | intron-variant | HERC2 | GRCh38.p7 | 15:28250810 | AGTGTCTACCCATGC[A/G]GGAGAGGGACACATG | 8924 |
rs12912618 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28235896 | GGAAATGCACAACTA[C/T]ATGAAAGAAAATGTA | 8924 |
rs12913692 | snp | A/C | 0.32955 | 0.237006 | intron-variant | HERC2 | GRCh38.p7 | 15:28119246 | TAAAAATACAAAAAA[A/C]AAAATTAGCCTGGCA | 8924 |
rs12913832 | snp | A/G | 0.29175 | 0.246489 | HERC2 | 15 | allele_origin=G(germline)/A(germline) | 15:28120472 | TCATTTGAGCATTAA[A/G]TGTCAAGTTCTGCAC | 8924 |
rs12915013 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28284949 | aaaaaaaaaaaaaaa[A/G]gataattaccaggaa | 8924 |
rs12915877 | snp | G/T | 0.133435 | 0.221162 | intron-variant | HERC2 | GRCh38.p7 | 15:28151748 | TCACATATGTTCCAA[G/T]CCATGAGTTCATAAT | 8924 |
rs12916300 | snp | C/T | 0.299411 | 0.245069 | intron-variant | HERC2 | GRCh38.p7 | 15:28165345 | ACTGTAAGTAAATAG[C/T]CTGCTGATGACAGGA | 8924 |
rs13379533 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | HERC2 | GRCh38.p7 | 15:28220257 | TTCCAGCCAGATCGC[C/T]GGATCCCACAGCCAC | 8924 |
rs13379587 | snp | A/G | 0.439641 | 0.162899 | intron-variant | HERC2 | GRCh38.p7 | 15:28218108 | CAGTTTGATGAGGTT[A/G]AATGATGTCCTTATG | 8924 |
rs13379928 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28311221 | tgtaatcccagcagt[C/T]tgggaggccgaggtg | 8924 |
rs13380156 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | HERC2 | GRCh38.p7 | 15:28210039 | gcaatccgcacacac[G/T]gcaacctccgccccc | 8924 |
rs13380224 | snp | G/T | 0.153332 | 0.230554 | intron-variant | HERC2 | GRCh38.p7 | 15:28310570 | TTGACTCTTCTAGTC[G/T]TCAGTCAGAGGAGGG | 8924 |
rs13380280 | snp | C/T | 0.210909 | 0.246925 | intron-variant | HERC2 | GRCh38.p7 | 15:28218120 | gttgaatgatgtcct[C/T]atgaaaaggggagat | 8924 |
rs16950927 | snp | G/T | 0.259951 | 0.249802 | intron-variant | HERC2 | GRCh38.p7 | 15:28245222 | TTCAGTACTTAACAA[G/T]GATTACTAATGGAAA | 8924 |
rs16950930 | snp | C/T | 0.16618 | 0.23553 | intron-variant | HERC2 | GRCh38.p7 | 15:28248326 | ACAGGATGCTATTAC[C/T]GATGTCTAAAGAATT | 8924 |
rs16950941 | snp | A/G | 0.259951 | 0.249802 | intron-variant | HERC2 | GRCh38.p7 | 15:28257598 | CTCTAACTAGACAAC[A/G]AATTGTTAGATGCAT | 8924 |
rs16950949 | snp | A/G | 0.255782 | 0.249933 | intron-variant | HERC2 | GRCh38.p7 | 15:28261687 | GGGGAATATAAACAA[A/G]AAGGCAAATGAAATT | 8924 |
rs16950960 | snp | A/G | 0.166506 | 0.235645 | intron-variant | HERC2 | GRCh38.p7 | 15:28264693 | AACTACACATAAAGA[A/G]TGCAAGGCTAATCTC | 8924 |
rs16950972 | snp | A/G | 0.1652 | 0.235179 | intron-variant | HERC2 | GRCh38.p7 | 15:28274123 | ATCATAAATCAAATC[A/G]CCTGAAAAGCTGAGA | 8924 |
rs16950975 | snp | A/G | 0.0122763 | 0.0773785 | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28274365 | GGACACGGTGCTCTC[A/G]TCAAAGAGCGAGGCC | 8924 |
rs16950979 | snp | A/G | 0.258288 | 0.249863 | intron-variant | HERC2 | GRCh38.p7 | 15:28275360 | GGGAGACCAGGCCGG[A/G]GAAGAGCTGGAAGAA | 8924 |
rs16950987 | snp | A/G | 0.444 | 0.157683 | intron-variant | HERC2 | GRCh38.p7 | 15:28281082 | TGCATGACTCATGAA[A/G]CACATTTATGGACAT | 8924 |
rs16950993 | snp | A/G | 0.440057 | 0.162414 | intron-variant | HERC2 | GRCh38.p7 | 15:28286974 | ATAGAGGGACAAAAA[A/G]GTGGAGAGAGCGGTG | 8924 |
rs28410461 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HERC2 | GRCh38.p7 | 15:28222290 | CACACAAAACATTCA[A/C]AAAGTACTAATGAAG | 8924 |
rs28411296 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28236917 | ATGGCACTTACAGTT[A/C]AAAAAAAATAATCTG | 8924 |
rs28430367 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28236916 | AATGGCACTTACAGT[C/T]CAAAAAAAATAATCT | 8924 |
rs28439160 | snp | A/G | | | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28178901 | CCTGAGTGAACAGCC[A/G]CCTTCTTGACCACGT | 8924 |
rs28441187 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28311472 | CCTGACTTAAAAAAC[A/C]AAAAAAGAAACTATT | 8924 |
rs28457230 | snp | G/T | 0.138147 | 0.223582 | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28272308 | GGCGCTGGTGCCCTG[G/T]GCGGAACGCTCATTG | 8924 |
rs28488374 | snp | C/T | 0.311614 | 0.242289 | intron-variant | HERC2 | GRCh38.p7 | 15:28205372 | AATGAACCTTCACCT[C/T]GGAGGTTCCCAGACC | 8924 |
rs28499292 | snp | A/G | 0.311614 | 0.242289 | intron-variant | HERC2 | GRCh38.p7 | 15:28205373 | ATGAACCTTCACCTT[A/G]GAGGTTCCCAGACCT | 8924 |
rs28516938 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | HERC2 | GRCh38.p7 | 15:28173840 | CAATAACAAAAAGAA[A/G]ACATGCAAACTGATC | 8924 |
rs28520578 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28115302 | CAAAGGTGGTCCACA[C/G]CCAACAGCCTCTGCG | 8924 |
rs28529816 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28148308 | ATCAAATAAACACAG[A/C]AGATGCTACCTTAAG | 8924 |
rs28539658 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28204927 | CAAAAAGAGCAAGGC[A/G]GGGGGAAAAAACAAT | 8924 |
rs28548731 | snp | C/G/T | 1.66821e-05 | 0.00288804 | missense | HERC2 | GRCh38.p7 | 15:28115463 | GTGAGGCTCATCCCA[C/G/T]CCAGCTGCTTCCAGA | 8924 |
rs28560468 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28291488 | TAATAGTGGCTAACT[C/T]TTAGAGGAAAGCTGA | 8924 |
rs28561443 | snp | A/G | 0.067446 | 0.170804 | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174002 | tttcatggatcatac[A/G]tattccaaagtcaat | 8924 |
rs28564562 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | HERC2 | GRCh38.p7 | 15:28136426 | GCTTCTGGCGGGGAG[G/T]GTGTGAGGCTCTCTG | 8924 |
rs28569339 | snp | G/T | 0.16618 | 0.23553 | intron-variant | HERC2 | GRCh38.p7 | 15:28287345 | TCCAAGCCCCTTCAA[G/T]GCTGCCAGGTAGAGA | 8924 |
rs28587058 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | HERC2 | GRCh38.p7 | 15:28173838 | AACAATAACAAAAAG[A/C]AAACATGCAAACTGA | 8924 |
rs28627850 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28291902 | AGAACAAGACTCCGT[C/T]TCAAAGGAAAAAAAA | 8924 |
rs28653336 | snp | C/T | 0.255782 | 0.249933 | intron-variant | HERC2 | GRCh38.p7 | 15:28165474 | ACCGGTGGTTTTCCA[C/T]GTACGTAAATATATA | 8924 |
rs28654205 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301737 | GTTGTATGTATGTGT[A/G]TATATATATATATAT | 8924 |
rs28661516 | snp | A/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28310464 | AAATTTTAATTTAAA[A/T]TTAAAAAATTAAAAT | 8924 |
rs28670140 | snp | A/G | 0.215144 | 0.247558 | intron-variant | HERC2 | GRCh38.p7 | 15:28137045 | ACAACCAAAACAACA[A/G]CAATAATGTCTATGG | 8924 |
rs28687537 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HERC2 | GRCh38.p7 | 15:28280778 | AGCCGAGTGTGGTGA[C/T]GCACGCCTGGAATTC | 8924 |
rs28690115 | snp | C/T | 0.252983 | 0.249982 | intron-variant | HERC2 | GRCh38.p7 | 15:28150998 | AGTAAAACTAAGACT[C/T]GAAGACTGAAAGAAA | 8924 |
rs28744636 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28173828 | ACCAAACAACAACAA[C/T]AACAAAAAGAAAACA | 8924 |
rs28784029 | snp | C/T | 0.128288 | 0.218372 | intron-variant | HERC2 | GRCh38.p7 | 15:28156194 | TTTGAGGTCAGGTAG[C/T]GTGATGCCTCCAGCT | 8924 |
rs28818860 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28137729 | GACACAACTTATTGA[A/C]ATAAGGCCACTTAAT | 8924 |
rs28823941 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28308404 | TTGTATGTTGATTTC[C/G]TATACTGCAATTGTA | 8924 |
rs28842779 | snp | G/T | 0.0821764 | 0.185298 | intron-variant | HERC2 | GRCh38.p7 | 15:28157964 | CTCGTTGGTTTCAAA[G/T]AACAACTTTATTTCT | 8924 |
rs28865032 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28308234 | TAATGTCTTTCATCA[C/G]CGTTTTAGAGTTTTC | 8924 |
rs28884789 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28284711 | GTGGATCTCAGGAGT[C/T]TGAGACCAGCCTGGC | 8924 |
rs33984228 | in-del | -/CT/GA | | | intron-variant | HERC2 | GRCh38.p7 | 15:28132051 | GGCCCTGGGGGCCCG[-/CT/GA]ACTGCGGTGAGCTGG | 8924 |
rs34034266 | snp | A/C | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28292521 | TACTGCTTCCTCAAA[A/C]AGTTACACGTAGTGC | 8924 |
rs34086791 | snp | G/T | 0.388587 | 0.208071 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28316781 | TTTTATCTACTGATC[G/T]TTTTTATTTTTTTTG | 8924 |
rs34095334 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28117933 | GTCTGGAAGGATGTC[-/A]AAAAGAAAAATTGAA | 8924 |
rs34116023 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28246387 | TAATGCTCTAACCTC[-/A]AAAAGTTAAAACATA | 8924 |
rs34181740 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28249059 | ATTCCCAATGTTTAA[-/G]GGAATGTAAACATTA | 8924 |
rs34192629 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28277463 | AATCCACAATTATCT[-/A]AAAAAAAAAAAAAAA | 8924 |
rs34199704 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28179640 | TTTTAAGCTAACTGT[-/A]AAAAGCCTGCGGCTG | 8924 |
rs34218394 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28222488 | GGAATTACTCCCCCC[-/A]AAAAAGCAAAATAAC | 8924 |
rs34228923 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28119129 | AAAAAGGCTGGGTGC[-/A]GGTGGCTCATGCCTA | 8924 |
rs34234048 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28230564 | AATTTTAAATTAAGA[A/C]ATACTTAGATTTACA | 8924 |
rs34255439 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28280551 | CACAGAGGAGTGCGG[-/C]CACATGACAGAGACT | 8924 |
rs34261044 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC2 | GRCh38.p7 | 15:28149080 | ACGAGACTCCTAACC[A/G]AGAACATCACCAAGA | 8924 |
rs34275052 | in-del | -/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28237854 | CCAAAGTTTAACCTC[-/T]TTTTCTTGTGGAACA | 8924 |
rs34290977 | snp | C/T | 1.76474e-05 | 0.00297042 | intron-variant | HERC2 | GRCh38.p7 | 15:28230362 | AATCACAGAAAATAC[C/T]GCACCTTGGGTGATT | 8924 |
rs34316772 | in-del | -/AG | 0.093777 | 0.195178 | intron-variant | HERC2 | GRCh38.p7 | 15:28138051 | AGCTAATCCAGAGCT[-/AG]TGCTAACTGTCTTCA | 8924 |
rs34318590 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28143379 | AGAATATCAAAGTCC[-/A]ACTTGAACTCAGTAT | 8924 |
rs34325054 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28220162 | ATGAGACTCACTGGT[-/G]GGTGCAGCTGCCCCG | 8924 |
rs34333172 | in-del | -/A | 0.245061 | 0.249951 | intron-variant | HERC2 | GRCh38.p7 | 15:28188543 | GTGAGACTCCGTCTT[-/A]AAAAAAAAAAAAAAA | 8924 |
rs34352282 | in-del | -/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28308237 | TGTCTTTCATCAGCG[-/T]TTTAGAGTTTTCATT | 8924 |
rs34411133 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28167654 | ATTTAAGATTATTTC[A/C]CAATACAAAGTTAAA | 8924 |
rs34422492 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28254487 | CATCAATTTCTTTTT[-/A]CCTTCTGTGCTTCTT | 8924 |
rs34423020 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | HERC2 | GRCh38.p7 | 15:28286308 | AATATTAGGTACTGT[A/C]CCTAAAGACAGTACA | 8924 |
rs34473600 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28223339 | CTCCAGGTGGGCGGG[-/A]AAAAGACCCAAACAG | 8924 |
rs34513876 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28292231 | CCAAACTCCATCTCC[-/A]AAAAAAAAAAAAAAA | 8924 |
rs34534946 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28119995 | CCTGAGAGCCCCTGG[-/C]CCCAAAAAGTCTGCG | 8924 |
rs34551935 | in-del | -/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28295319 | TGTGTGGGGGGGGGG[-/G]AGTGGGGGGGAGGCG | 8924 |
rs34556165 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28264963 | ATTTTTCATCTTTCA[-/C]CTAAGAAATGCCCAA | 8924 |
rs34563035 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28138000 | TGTTTGGCATAGACA[-/G]GAAGATCAAAACGGA | 8924 |
rs34565964 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28277176 | GTTGCCAGCAGTTAA[A/G]GTGGGGAGAGAAGAC | 8924 |
rs34581185 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28287120 | AAAAATAAACCTGTG[-/A]AAAAGGAAGCTTTAG | 8924 |
rs34582496 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28132039 | GTTTTCCCAGAGGGG[-/C]CCTGGGGGCCCCTGA | 8924 |
rs34590466 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28184227 | ACACACATATATATA[-/C]CACACATATATGTAT | 8924 |
rs34632582 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28293493 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8924 |
rs34639657 | in-del | -/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28249815 | CCACGCCAAGCTAAC[-/T]TTTTTTTTTTTTTTT | 8924 |
rs34662382 | snp | A/G | 0.0190234 | 0.0956547 | intron-variant | HERC2 | GRCh38.p7 | 15:28177394 | GTTTCTTATTAGCAA[A/G]TGAGACTAAAAAAAG | 8924 |
rs34668548 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28230568 | TTAAATTAAGAAATA[C/T]TTAGATTTACATGAA | 8924 |
rs34755180 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28243622 | ATTAATGCACACAGG[-/C]AAAAGGTATCAAACC | 8924 |
rs34800540 | snp | C/T | 0.375 | 0.216506 | intron-variant | HERC2 | GRCh38.p7 | 15:28225435 | AGTCAAGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8924 |
rs34823420 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28257478 | CATTTGGCCATACCT[-/A]AAAAAGTAAAAGCAT | 8924 |
rs34823980 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28264021 | AAAACTTTGTCTTAC[-/A]AAAAAAAAAAAAAAA | 8924 |
rs34882509 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28167864 | GGGAAGTTTAAGTGG[-/A]AAAAACTCAGCAACA | 8924 |
rs34910683 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28242599 | AATTACAGGTCACTG[-/A]AAAAATTACAAGGAA | 8924 |
rs34917808 | in-del | -/A | 0.491629 | 0.0641526 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300052 | GCGAGACTCGGTGTT[-/A]AAAAAAAAAAAAAAA | 8924 |
rs34929117 | in-del | -/C | | | splice-donor-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214075 | GAGAACACAAACCCA[-/C]CCCTTCGGAAGGCCT | 8924 |
rs34984960 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28179574 | CTATATATTCACTCT[-/C]CCTGTACTTTCTATC | 8924 |
rs34994916 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28272872 | CTTCCCCAAAGCATT[-/C]CCCGGTCTGCACCAG | 8924 |
rs35047502 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28244087 | GGATCTGCTTGAGCC[-/G]GGGGAGGTCAAGGCT | 8924 |
rs35086998 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28181787 | CCTCTCATCCAAGTA[-/C]CTAGGGGATGAAGGA | 8924 |
rs35092122 | in-del | -/A | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28283033 | AAGAAATGTCCCAGC[-/A]AAAAAAAAAAAAAAA | 8924 |
rs35097050 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28223118 | CCCTGACAATTGGTG[-/C]CCTGGGTGGCTACAG | 8924 |
rs35108980 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28228093 | TAAAATGGTACACTT[-/C]CCTATTTGTGTCTTA | 8924 |
rs35239380 | in-del | -/A | 0.302936 | 0.244331 | intron-variant | HERC2 | GRCh38.p7 | 15:28296690 | GAATTACTGATACAT[-/A]AAAAAAAAAAAAAAA | 8924 |
rs35299892 | in-del | -/T | 0.471863 | 0.115225 | intron-variant | HERC2 | GRCh38.p7 | 15:28296083 | TATTGAATGTCAAAA[-/T]TATCTCCCTAACACC | 8924 |
rs35323513 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28244192 | ACATATTTACTTTAA[-/C]CCTAAACCTGGAAAC | 8924 |
rs35324937 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28281924 | AGAGCCCAGAAACAA[-/C]CCCCAAAGCTCCAAG | 8924 |
rs35337128 | in-del | -/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28232219 | TGGTCAATAAGCAGG[-/T]TTTGTGAGTAAATCA | 8924 |
rs35387999 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28266042 | ATTAATGTTAACAAA[-/A]GGAAATTCACTATCC | 8924 |
rs35473260 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28242540 | TAGTAAAGGGGTGGT[-/G]GGTTATCAATAACAA | 8924 |
rs35502049 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28255173 | ACACCTTGTCTCTAC[-/A]AAAAAATCACAAAAC | 8924 |
rs35530455 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28190048 | AGTCTGGCTCTGTCG[-/C]CCCAGGCTGGAGTGC | 8924 |
rs35531980 | snp | G/T | 0.0737376 | 0.17729 | intron-variant | HERC2 | GRCh38.p7 | 15:28127755 | CTCCCAGACAACGGG[G/T]ACACACAAAAAGGGG | 8924 |
rs35596851 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28217072 | GGCACTCATACACAT[G/T]TACACAAATGCTCGC | 8924 |
rs35615080 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC2 | GRCh38.p7 | 15:28121600 | GAACAGGCTGGCCCC[A/G]AAGCACACAGGGACA | 8924 |
rs35629645 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28225715 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAAAAAGA | 8924 |
rs35633119 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28310602 | GTGAATACATGCACT[-/G]GGGGTTCAGTCCAAA | 8924 |
rs35639835 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28227251 | CTGTGCTCCAGCCTA[-/G]GCGACGGAGTGAGAC | 8924 |
rs35663783 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28241792 | ACCACTGCACTCCAA[-/C]CTGGGCGACAGAGCA | 8924 |
rs35694468 | in-del | -/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28187371 | GAATCTTGCTTGTTG[-/C]CCCAGGCTGGAGTGC | 8924 |
rs35772638 | in-del | -/G | | | utr-variant-3-prime | HERC2 | GRCh38.p7 | 15:28111535 | GTAATGCAGCATTAC[-/G]GGGTGAGAAGACCCT | 8924 |
rs35809371 | in-del | -/AC | | | intron-variant | HERC2 | GRCh38.p7 | 15:28224134 | AAATTAAAAAATTAT[-/AC]ACACACACACACACA | 8924 |
rs35818659 | in-del | -/AG/CACACACA | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28224164 | CACACACACACACAC[-/AG/CACACACA]ACAGAGAGAGAGAGA | 8924 |
rs35878839 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28181671 | CACTAAGTAATACAA[-/G]GGAATGCTGAATTCA | 8924 |
rs35881932 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28133617 | ATTTTGAATTAATGT[-/G]TTGGATATGGTGTAA | 8924 |
rs35946704 | snp | G/T | 0.320335 | 0.239902 | intron-variant | HERC2 | GRCh38.p7 | 15:28173902 | GCAGGAAGGAGGGAG[G/T]TAAAAGCAAAAGGGA | 8924 |
rs35995546 | in-del | -/AA | | | intron-variant | HERC2 | GRCh38.p7 | 15:28259989 | AAAAAAAAAAAAAAA[-/AA]GAGTAGTAAATTGTG | 8924 |
rs35999513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC2 | GRCh38.p7 | 15:28292530 | CTCAAACAGTTACAC[A/G]TAGTGCCAGGTGCGA | 8924 |
rs36035563 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28198639 | CTAACCCAGTAGGTG[-/C]CCCCTTTCTGCTGCC | 8924 |
rs36047605 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28121731 | ACAGGGCACAGAACA[-/G]GGGAGGGCTGGGCCT | 8924 |
rs36068402 | in-del | -/T/TT/TTT | 0.498459 | 0.0277128 | intron-variant | HERC2 | GRCh38.p7 | 15:28129780 | TAAGCCTTTGCCTCC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 8924 |
rs36072010 | snp | C/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28292462 | GGAACCTTAGTATAC[C/T]GCTGCAAGAATATAA | 8924 |
rs36082394 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28177557 | GGCAGGGAACAGAAA[-/A]GCCCACAGCATAGCT | 8924 |
rs36126627 | in-del | -/AT | | | intron-variant | HERC2 | GRCh38.p7 | 15:28245606 | CACACACACACACAG[-/AT]ATATATATATACACA | 8924 |
rs55658008 | snp | C/G | 0.158302 | 0.232576 | intron-variant | HERC2 | GRCh38.p7 | 15:28159936 | CCTTTCTGTTTGTTA[C/G]TTTTCCTTCTAACAG | 8924 |
rs55685709 | snp | A/G | 0.158632 | 0.232706 | intron-variant | HERC2 | GRCh38.p7 | 15:28149998 | ACCGAGAACGGCCAC[A/G]CGAACACACATTCTA | 8924 |
rs55840834 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28204634 | AAAAAAAAAAAAAAA[-/A]GATAGACTTAAAGGA | 8924 |
rs55907941 | snp | A/T | 0.243919 | 0.249926 | intron-variant | HERC2 | GRCh38.p7 | 15:28169346 | TCACCATCAAAGAAC[A/T]TGTGACTTACAACAT | 8924 |
rs55912569 | snp | A/G | 0.186105 | 0.241697 | intron-variant | HERC2 | GRCh38.p7 | 15:28227921 | CAAATCCATAGACAG[A/G]GAAAGCAGATTTGTG | 8924 |
rs55925927 | snp | A/G | 0.15665 | 0.231917 | intron-variant | HERC2 | GRCh38.p7 | 15:28288698 | TAAAAATACAAAAAC[A/G]TTAGCCAGGCACGGT | 8924 |
rs55935219 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28290524 | CATGAGCCACCACAC[A/G]CAGCTACATTCTTAT | 8924 |
rs55954378 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28161227 | TTCAGAATTTCAGAT[A/G]AAGGAGTATGAACTT | 8924 |
rs55977156 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301779 | TATATATATATATAT[-/AT]GGGTTATATATTCTA | 8924 |
rs55998000 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301398 | CCAGCCTGGGTGACA[A/G]AGCAAGACTTTACCT | 8924 |
rs56013620 | snp | A/G | 0.255224 | 0.249945 | intron-variant | HERC2 | GRCh38.p7 | 15:28143128 | AAGAACATAAACACT[A/G]AAATAAAAAAGAGGA | 8924 |
rs56087567 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28121875 | AGGGAGCACCGCGGA[A/G]CCAGCCGGACCTTGG | 8924 |
rs56097147 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28153835 | AAGGAGCACCCAGTA[A/G]GTGAAAATGACCACA | 8924 |
rs56156327 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28171425 | CAGAAAGGAGAAGAT[A/G]AGAGTCAAGC | 8924 |
rs56171895 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | HERC2 | GRCh38.p7 | 15:28116161 | CGGAAGTCAACAGCA[C/T]CTCGTTCGCTTCCAC | 8924 |
rs56220910 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28311388 | AGGATCACCTGAGCC[C/T]GGGGAGGTTAAGGCT | 8924 |
rs56240434 | snp | A/G | 0.165853 | 0.235413 | intron-variant | HERC2 | GRCh38.p7 | 15:28253149 | TCACCTTGCTTTTTC[A/G]CTCTTCTTGGGTGAT | 8924 |
rs56285658 | snp | A/G/T | 0.104859 | 0.203554 | intron-variant | HERC2 | GRCh38.p7 | 15:28294065 | CTATCTAAAAATCTC[A/G/T]AAGGAAACAGTTCCT | 8924 |
rs56314524 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28185122 | ACTATTTTCTTTTCA[-/A]CTTCTACACAAAGTT | 8924 |
rs56343125 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28121940 | AGGGAGCACCGCGGA[A/G]CCAGCCGGACCTTGG | 8924 |
rs56672715 | in-del | -/A/AAAA | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28188558 | AAAAAAAAAAAAAAA[-/A/AAAA]GAGTACTTGTTAGAG | 8924 |
rs56685874 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HERC2 | GRCh38.p7 | 15:28252899 | ACAGCAGGCCCACCC[C/T]ACGCCACAGGCCCAA | 8924 |
rs56723434 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28201698 | TCTTCATTTAAAAAA[-/A]GACTAATAGCAGTAG | 8924 |
rs56743903 | snp | A/G | 0.339882 | 0.233284 | intron-variant | HERC2 | GRCh38.p7 | 15:28173939 | CAGAGGGCCAGAGAG[A/G]AACGCTGGGGTAGTG | 8924 |
rs56781260 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28258632 | ATCATTATCTATTAC[-/A]AAAAAAAGATAGGTC | 8924 |
rs56809329 | snp | A/G | 0.241914 | 0.249869 | intron-variant | HERC2 | GRCh38.p7 | 15:28186950 | CAAAAGAAGTGGTCA[A/G]CTCATCAAGATGTCT | 8924 |
rs56842627 | snp | A/G | 0.157972 | 0.232445 | intron-variant | HERC2 | GRCh38.p7 | 15:28225575 | TGGTGGCGCGTGCCT[A/G]TAGTCCCAGCTACTC | 8924 |
rs56891387 | snp | A/G | 0.245631 | 0.249962 | intron-variant | HERC2 | GRCh38.p7 | 15:28159357 | GGTTCCATTCTCCCC[A/G]TCACTTTCAGGTGCA | 8924 |
rs56943892 | snp | A/G | 0.267908 | 0.249358 | intron-variant | HERC2 | GRCh38.p7 | 15:28311231 | GCAGTCTGGGAGGCC[A/G]AGGTGGGCAGACTGC | 8924 |
rs57039476 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | HERC2 | GRCh38.p7 | 15:28144598 | ACTACGTGGACATGT[A/G]CACGTGTCCCTGTTG | 8924 |
rs57079108 | snp | C/T | 0.262985 | 0.249663 | intron-variant | HERC2 | GRCh38.p7 | 15:28174828 | CCATGAAAATGCTTG[C/T]TAATACCTATAAAAG | 8924 |
rs57135799 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28295310 | TCCTACATGTGTGTG[G/T]GGGGGGGGGAGTGGG | 8924 |
rs57175487 | snp | C/T | 0.0444908 | 0.142359 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301017 | CAGATTTTGGTCTCT[C/T]AGAACCATTTCCCAA | 8924 |
rs57179075 | snp | A/C | 0.165853 | 0.235413 | intron-variant | HERC2 | GRCh38.p7 | 15:28260375 | CTCCCTTAATCTGAT[A/C]ATAAGGCATCTACAT | 8924 |
rs57186964 | snp | A/G | 0.1652 | 0.235179 | intron-variant | HERC2 | GRCh38.p7 | 15:28279092 | CACCTCCCGGGATCA[A/G]GCAATTCTCCTGCCT | 8924 |
rs57189560 | snp | A/C/T | 0.0492775 | 0.149034 | intron-variant | HERC2 | GRCh38.p7 | 15:28248542 | CACTTTCACATTTTA[A/C/T]GCAACTTACTAGAAA | 8924 |
rs57252238 | snp | A/C | 0.165527 | 0.235296 | intron-variant | HERC2 | GRCh38.p7 | 15:28279250 | CACCTCAGGCCTCCC[A/C]AAGTGCTGGGATTAC | 8924 |
rs57291038 | snp | C/G | 0.26518 | 0.249539 | intron-variant | HERC2 | GRCh38.p7 | 15:28307871 | TCACCGTAGATGTGC[C/G]GATTTGTTTCTGGAT | 8924 |
rs57299794 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | HERC2 | GRCh38.p7 | 15:28236223 | ATGACAACCACTCAC[A/T]GCTGTTTCTACCTGA | 8924 |
rs57305391 | snp | C/G | 0.157972 | 0.232445 | intron-variant | HERC2 | GRCh38.p7 | 15:28227920 | GCAAATCCATAGACA[C/G]GGAAAGCAGATTTGT | 8924 |
rs57318871 | snp | A/G | 0.0897869 | 0.191916 | intron-variant | HERC2 | GRCh38.p7 | 15:28202088 | CAGCGGCCCAGGTGC[A/G]GGCGGTCACATGGGA | 8924 |
rs57487014 | snp | G/T | 0.0524604 | 0.153226 | intron-variant | HERC2 | GRCh38.p7 | 15:28180406 | TCATTAAGTAATGCA[G/T]GACTGTACTACTAAT | 8924 |
rs57518203 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301162 | GCTCACGCCTATAAT[C/T]CTAGCATTTTGGGAG | 8924 |
rs57556554 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28258625 | GCATCAAATCATTAT[C/T]TATTACAAAAAAAAG | 8924 |
rs57577849 | snp | C/T | 0.168135 | 0.236216 | intron-variant | HERC2 | GRCh38.p7 | 15:28309166 | TTCTAGAAATATCTA[C/T]TAAATCCATTTGGTC | 8924 |
rs57641774 | snp | A/G | 0.396 | 0.202938 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28215440 | AAAAGCAGGTAAACT[A/G]AAGGTTAGCAACTTA | 8924 |
rs57652144 | in-del | -/G | | | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28313475 | ACCCAGCCCGTTAAG[-/G]CATTTATTAAAGTGA | 8924 |
rs57696757 | in-del | -/AAAAA | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300849 | AAAAAAAAAAAAAAA[-/AAAAA]TTAAGGTTTTCAGTG | 8924 |
rs57713848 | snp | A/G | 0.165853 | 0.235413 | intron-variant | HERC2 | GRCh38.p7 | 15:28239923 | CAACACAGAGAACAT[A/G]CTCAGGTCCTAATTC | 8924 |
rs57727285 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | HERC2 | GRCh38.p7 | 15:28238473 | GATAAGACAGACATC[A/G]AAGCCACAGATACAT | 8924 |
rs57936799 | in-del | -/CTCA | | | intron-variant | HERC2 | GRCh38.p7 | 15:28217223 | ATCCCCTCACACTCA[-/CTCA]TGCCTCCCTCATGCT | 8924 |
rs57980844 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300758 | AACCCAGGAGGCAGA[A/G]GTTTCAGTGAGCCGA | 8924 |
rs58138907 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | HERC2 | GRCh38.p7 | 15:28282146 | AGGCAAAGTGGGAAG[A/C]CTGGACTTCGTCTCC | 8924 |
rs58164482 | snp | C/T | 0.433236 | 0.170072 | intron-variant | HERC2 | GRCh38.p7 | 15:28177673 | TTAGCAGGAAAGCTT[C/T]CTGGGACATATGTGC | 8924 |
rs58172384 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | HERC2 | GRCh38.p7 | 15:28127087 | GGATTGTCAAATCCA[A/G]AGAGACTCCTCGGGT | 8924 |
rs58255711 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HERC2 | GRCh38.p7 | 15:28229064 | AAGCTGACAGCAGCA[C/T]AGATTATACAAGTAC | 8924 |
rs58278950 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC2 | GRCh38.p7 | 15:28210729 | CTAACACATACCTGC[A/G]TGCCACCAATCTTGC | 8924 |
rs58358300 | snp | A/C | 0.257454 | 0.249889 | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174247 | TATAAATCGCATGAG[A/C]GCACACCATAATTCT | 8924 |
rs58395411 | snp | C/G | 0.260504 | 0.249779 | intron-variant | HERC2 | GRCh38.p7 | 15:28290973 | TAATAAAGAGTAAAG[C/G]AGAAATCAATGAAAA | 8924 |
rs58424834 | snp | C/T | 0.262985 | 0.249663 | intron-variant | HERC2 | GRCh38.p7 | 15:28197658 | TCTGGAGGCTGAGAC[C/T]GGAGAATTCCTTAAA | 8924 |
rs58447102 | in-del | -/CACACA | | | intron-variant | HERC2 | GRCh38.p7 | 15:28279651 | ACACACACACACACA[-/CACACA]AATTGTTTTTATTTA | 8924 |
rs58488922 | in-del | -/A | 0.00335883 | 0.0408428 | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174352 | CTATAAGGTTGCTGT[-/A]AACCTACAGAAAAAT | 8924 |
rs58523311 | snp | C/T | 0.1652 | 0.235179 | intron-variant | HERC2 | GRCh38.p7 | 15:28151888 | AGCACCTTGAACAAC[C/T]AACTACAGGATGAAG | 8924 |
rs58617687 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28133154 | TAAAAAAAAAAAAAA[-/A]GAATCATATGCAACT | 8924 |
rs58656163 | snp | A/C/G/T | 0.013956 | 0.0823718 | intron-variant | HERC2 | GRCh38.p7 | 15:28117239 | GCACTGGCGAATGCA[A/C/G/T]GAGGAGGAGGCACCG | 8924 |
rs58670424 | in-del | -/AG | | | intron-variant | HERC2 | GRCh38.p7 | 15:28277478 | TAAAAAAAAAAAAAA[-/AG]GGGCTTTTTTAAAAT | 8924 |
rs58686616 | snp | A/G | 0.167809 | 0.236103 | intron-variant | HERC2 | GRCh38.p7 | 15:28309284 | TCCATCTATTAATGT[A/G]TTAAGGCCTATCTCT | 8924 |
rs58762968 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301031 | TCAGAACCATTTCCC[A/C/G]ATAAAAGACGCTAGG | 8924 |
rs58764974 | snp | G/T | 0.286303 | 0.24735 | intron-variant | HERC2 | GRCh38.p7 | 15:28287156 | CATATCTAAGCAAAA[G/T]AAAAAACAAATTCTA | 8924 |
rs58793311 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | HERC2 | GRCh38.p7 | 15:28150252 | TCTAGTAAAATTACC[A/G]AAGAAACACACGCGG | 8924 |
rs58875335 | snp | A/C | 0.134119 | 0.221521 | intron-variant | HERC2 | GRCh38.p7 | 15:28218422 | ACACCCACCCACATG[A/C]ACACCCAGACACAAG | 8924 |
rs58921212 | snp | A/T | 0.215631 | 0.247626 | intron-variant | HERC2 | GRCh38.p7 | 15:28211160 | CCTGCGGAAGGAAAG[A/T]CTCAGTGAGAAGGGC | 8924 |
rs58995112 | in-del | -/A | 0.353154 | 0.227726 | intron-variant | HERC2 | GRCh38.p7 | 15:28232551 | GAAAAAAAAAAAAAA[-/A]GAATATAATCAGAAA | 8924 |
rs59027140 | snp | G/T | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28186897 | TATCAACTGAGTTAC[G/T]CAAAGTTAATGCAGC | 8924 |
rs59061827 | snp | A/C | 0.185155 | 0.241444 | intron-variant | HERC2 | GRCh38.p7 | 15:28284314 | GTAAACCACAGAGAG[A/C]CAGGAAGAACCAAAC | 8924 |
rs59120423 | snp | A/G | 0.444444 | 0.157135 | intron-variant | HERC2 | GRCh38.p7 | 15:28146675 | CTGTGGGAATGCCCA[A/G]TGTGCAGCCAAGTCA | 8924 |
rs59126013 | snp | A/T | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214436 | GCACTGCGCCGCTCT[A/T]CACCAGGGCACAGGG | 8924 |
rs59147074 | snp | C/T | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28178189 | CCCAGGAGATGGTGA[C/T]TGAAATGAGTGGGGC | 8924 |
rs59154112 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28272947 | GGCCAGGGCCAAGTG[C/T]TGGTCCTGCAGGGGG | 8924 |
rs59214152 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HERC2 | GRCh38.p7 | 15:28191590 | GAGGTGCCTCCACGC[A/G]TTGGTGTAATCACAA | 8924 |
rs59230967 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HERC2 | GRCh38.p7 | 15:28241439 | AATGGTGCAGCCACT[A/C]CGAAAAACACTATGG | 8924 |
rs59237367 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | HERC2 | GRCh38.p7 | 15:28147386 | GTAATCTTAGCACTT[C/T]GGGAGGCCGAGGCAG | 8924 |
rs59259834 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28300068 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 8924 |
rs59285055 | snp | C/T | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28314008 | CAGGTGAGTTAGAAG[C/T]AGACCAGCCTTTACG | 8924 |
rs59310062 | snp | C/T | 0.441841 | 0.160303 | intron-variant | HERC2 | GRCh38.p7 | 15:28208490 | TGTTTCAGATACTCC[C/T]ATACCTTCCTAGCAG | 8924 |
rs59368062 | snp | C/T | 0.105214 | 0.203807 | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174295 | ATAATGCAGTTAACA[C/T]GGCACTACAACCTCT | 8924 |
rs59474042 | snp | A/G | 0.166506 | 0.235645 | intron-variant | HERC2 | GRCh38.p7 | 15:28218319 | CTCAGCCTTCCAGCC[A/G]CCAGAACCGTGAGAA | 8924 |
rs59478290 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28284842 | ATCACTTGAACCCGG[G/T]GGGGTTGGAGGTTGC | 8924 |
rs59546649 | snp | A/C/T | 0.0471551 | 0.14613 | intron-variant | HERC2 | GRCh38.p7 | 15:28253185 | TTACACAACACTGAC[A/C/T]GTTTTGGCTTCTGCC | 8924 |
rs59556486 | snp | A/C | 0.0169009 | 0.0903593 | intron-variant | HERC2 | GRCh38.p7 | 15:28254290 | TCTGTCACACACACA[A/C]AAAAAAGTAAATAAA | 8924 |
rs59576796 | snp | C/G | | | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174150 | AGTCCTGTTCACACA[C/G]AAGGACAGCGCTGTG | 8924 |
rs59600059 | snp | A/G | 0.00774537 | 0.061747 | intron-variant | HERC2 | GRCh38.p7 | 15:28218443 | CAGACACAAGCGTGC[A/G]GCCCCCAGCGCTGAC | 8924 |
rs59603405 | snp | A/G | 0.117188 | 0.211804 | intron-variant | HERC2 | GRCh38.p7 | 15:28240383 | AGATCACGTCACTAC[A/G]CTCCCGCCTGGGCGA | 8924 |
rs59622763 | snp | C/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28307884 | GCGGATTTGTTTCTG[C/G]ATTCTCTATTCTGTT | 8924 |
rs59649986 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | HERC2 | GRCh38.p7 | 15:28225274 | AGACAAAAACAAAAA[A/G]ATACAAAGCAGAAAG | 8924 |
rs59660294 | snp | C/T | 0.166506 | 0.235645 | intron-variant | HERC2 | GRCh38.p7 | 15:28192768 | GCAAAGTCCCTGAGA[C/T]GACACATAGCATTTT | 8924 |
rs59671525 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28120192 | AACAACCTATTTATG[C/T]GAGGACGTGACTGAC | 8924 |
rs59673075 | snp | C/T | 1.66896e-05 | 0.00288869 | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28272227 | CACGTGCATGTCGCC[C/T]TCGGAGTGGGGTGCA | 8924 |
rs59916304 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174286 | TTTAGAGTCATAATG[C/T]AGTTAACATGGCACT | 8924 |
rs59929119 | snp | A/T | | | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301052 | AGACGCTAGGGCTCT[A/T]GGGAAAATAAGTAGA | 8924 |
rs60025758 | snp | C/T | 0.441977 | 0.16014 | intron-variant | HERC2 | GRCh38.p7 | 15:28238985 | GCATGAATACCAAAT[C/T]GGGCCATGCCAGGCC | 8924 |
rs60059865 | snp | G/T | 0.0498117 | 0.149749 | intron-variant | HERC2 | GRCh38.p7 | 15:28156596 | TGATTTTTGCACATT[G/T]ATTTTGTATCCTGAG | 8924 |
rs60100342 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HERC2 | GRCh38.p7 | 15:28282393 | GCAAATAATTAAAAA[C/T]GGTCACGATAAAAAG | 8924 |
rs60107275 | snp | A/G | 0.37955 | 0.213815 | intron-variant | HERC2 | GRCh38.p7 | 15:28136391 | CTCAGGTGGATAAAT[A/G]AGCCCCACCCCCAAA | 8924 |
rs60186418 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28293522 | AAAAAGAAACCAATA[C/T]AACAAATTATTTAAA | 8924 |
rs60188219 | in-del | -/TCTG | | | intron-variant | HERC2 | GRCh38.p7 | 15:28253182 | TTTTACACAACACTG[-/TCTG]ACCGTTTTGGCTTCT | 8924 |
rs60204463 | snp | C/T | 0.0179188 | 0.0929425 | intron-variant | HERC2 | GRCh38.p7 | 15:28222237 | GAGCGTCAAAAACAA[C/T]AGCTGAGCCAACAAG | 8924 |
rs60214216 | in-del | -/GAC | | | intron-variant | HERC2 | GRCh38.p7 | 15:28218434 | TGAACACCCAGACAC[-/GAC]AAGCGTGCGGCCCCC | 8924 |
rs60222071 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28251487 | AAGTAAAAAAAAAAA[-/A]CAAAAAAACACATAA | 8924 |
rs60298247 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | HERC2 | GRCh38.p7 | 15:28150755 | CCGAGAATGGCCACA[C/T]GAACGTATATTCTAG | 8924 |
rs60336835 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | HERC2 | GRCh38.p7 | 15:28122118 | CAGACCGGGGAGGGG[-/A]AACAAGGTCCTGGCT | 8924 |
rs60358372 | in-del | -/C | 0.16618 | 0.23553 | intron-variant | HERC2 | GRCh38.p7 | 15:28240869 | GGAGGTAGACCCTTA[-/C]CTTACGCCACACACA | 8924 |
rs60399863 | snp | G/T | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28313717 | AACATATAAAAAATG[G/T]TAAGAACAGGTTCCT | 8924 |
rs60409381 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28225260 | CTGTCTCAAAACAAA[A/G]ACAAAAACAAAAAAA | 8924 |
rs60422914 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | HERC2 | GRCh38.p7 | 15:28238471 | TTGATAAGACAGACA[C/T]CGAAGCCACAGATAC | 8924 |
rs60537567 | snp | A/G | 0.0333238 | 0.124705 | intron-variant | HERC2 | GRCh38.p7 | 15:28288987 | TGACACAGCAACACT[A/G]CCAACCAAGAACATG | 8924 |
rs60556622 | in-del | -/A | 0.441021 | 0.161279 | intron-variant | HERC2 | GRCh38.p7 | 15:28227275 | GTGAGACTCCGTCTC[-/A]AAAAAAAGTAAAATA | 8924 |
rs60656642 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | HERC2 | GRCh38.p7 | 15:28295900 | CTATGACAGAGACCA[C/T]AGGGTCCACTGAGAC | 8924 |
rs60694069 | snp | C/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28293539 | ACAAATTATTTAAAG[C/G]ATGTCTTCCAAAGTG | 8924 |
rs60751586 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28293552 | AGCATGTCTTCCAAA[A/G]TGATATTCCATCTAC | 8924 |
rs60794452 | in-del | -/A/AA | | | intron-variant | HERC2 | GRCh38.p7 | 15:28225715 | AAAAAAAAAAAAAAA[-/A/AA]GAAAGAAAAAAAAGA | 8924 |
rs60826150 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28231453 | TTGGGGCACTGGAGT[C/T]TGAGTGAGGTCAGTC | 8924 |
rs60860237 | in-del | -/CT | | | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174337 | CACAATTAAATAAAT[-/CT]ATAAGGTTGCTGTAA | 8924 |
rs60878621 | in-del | -/G | 0.36021 | 0.224397 | intron-variant | HERC2 | GRCh38.p7 | 15:28136334 | TGCACTGACATAATA[-/G]TAAGGAAGCCACAAG | 8924 |
rs60949565 | in-del | -/C | 0.442791 | 0.15916 | intron-variant | HERC2 | GRCh38.p7 | 15:28257455 | CACCCATTTCACTAG[-/C]CCCATCTCATTTGGC | 8924 |
rs60957324 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28287739 | TTTTTTTTTTTTTTT[G/T]GTTTGAGATGGAGTC | 8924 |
rs61011458 | snp | A/G | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28202922 | ATTACAGCCCCAAGC[A/G]AACAGTCACAGGGGC | 8924 |
rs61050110 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | HERC2 | GRCh38.p7 | 15:28197572 | GCCTGGCCAACATGG[G/T]GAAACCCCATCTCTA | 8924 |
rs61112679 | in-del | -/GAG | | | intron-variant | HERC2 | GRCh38.p7 | 15:28171983 | GGGAGGCTGAGGCAG[-/GAG]AATGGCGTGAACCCG | 8924 |
rs61118117 | in-del | -/TCTT | 0.1652 | 0.235179 | intron-variant | HERC2 | GRCh38.p7 | 15:28294882 | TCCCTAGGGCAGGAA[-/TCTT]CTAGGGTTATAAACA | 8924 |
rs61146234 | snp | A/G | 0.157972 | 0.232445 | intron-variant | HERC2 | GRCh38.p7 | 15:28225883 | AAACATAAATTACCC[A/G]AACTGACTCAAGAAG | 8924 |
rs61147405 | in-del | -/AC | | | intron-variant | HERC2 | GRCh38.p7 | 15:28147647 | TTTTCTGAATCTCAC[-/AC]CTCATTCTAAAAGTT | 8924 |
rs61181673 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174277 | TTCTGTGTCTTTAGA[G/T]TCATAATGCAGTTAA | 8924 |
rs61266109 | snp | C/T | 0.379942 | 0.213577 | intron-variant | HERC2 | GRCh38.p7 | 15:28136390 | ACTCAGGTGGATAAA[C/T]GAGCCCCACCCCCAA | 8924 |
rs61266141 | snp | A/G | 0.158302 | 0.232576 | intron-variant | HERC2 | GRCh38.p7 | 15:28131733 | CTGGCACCCCCAAGC[A/G]CGTGCCGTGGCAACT | 8924 |
rs61329240 | snp | A/C | 0.186421 | 0.24178 | intron-variant | HERC2 | GRCh38.p7 | 15:28224835 | TGAAATGAGAAATAA[A/C]AAAAAGAAAAGTGGA | 8924 |
rs61335644 | snp | A/G | 0.25045 | 0.25 | intron-variant | HERC2 | GRCh38.p7 | 15:28185212 | TTTATTACCAGAACT[A/G]CTACCCCCCACTTCT | 8924 |
rs61368565 | snp | A/G | 0.261332 | 0.249743 | intron-variant | HERC2 | GRCh38.p7 | 15:28136235 | CTAAATCAGACTGCC[A/G]TTTTCCAAATGAAGG | 8924 |
rs61381029 | in-del | -/GAGG | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28288454 | TTTGAACCCAGGAGG[-/GAGG]CAGAGGCTGCAGTGA | 8924 |
rs61460557 | snp | C/T | 0.443464 | 0.15834 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28215474 | ATTATCAAGGACCTC[C/T]GCCCCTTGCCTCCAG | 8924 |
rs61489954 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | HERC2 | GRCh38.p7 | 15:28177891 | TGAGAACTGTACCTC[A/G]ACAGTGAAATTATTC | 8924 |
rs61511707 | snp | A/G | 0.264084 | 0.249603 | intron-variant | HERC2 | GRCh38.p7 | 15:28171767 | TAGAAATAATCTAAC[A/G]AAAGACAAGCAAAAC | 8924 |
rs61585051 | snp | C/T | 0.261332 | 0.249743 | intron-variant | HERC2 | GRCh38.p7 | 15:28125243 | ACTAGGGCCAACAAA[C/T]GCATGGCTGCCAGTG | 8924 |
rs61590360 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28123929 | TTCCGTGAACATTTG[A/C]TGAATGAGCTGTATT | 8924 |
rs61659212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28189544 | AATTTCTTCACTTAT[A/T]AGCACCACTGGTATT | 8924 |
rs61660421 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28152962 | GGGCTTGGAGTTTGA[G/T]AAATTGAGTTCAAAT | 8924 |
rs61687434 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28155093 | TACAAAGCACATGAA[-/A]CTCATCCTTTTTTAT | 8924 |
rs61699528 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | HERC2 | GRCh38.p7 | 15:28149367 | CCAAAAAAACACACG[C/T]GGCTCCTAACCGAGA | 8924 |
rs61751203 | snp | C/T | 1.65762e-05 | 0.00287886 | missense, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28272994 | TGGTGGCTGGCGTTC[C/T]GTGAACATCCCTGAA | 8924 |
rs61751204 | snp | A/G | 0.000230863 | 0.0107414 | intron-variant | HERC2 | GRCh38.p7 | 15:28201557 | CAGCACCAGTAGACT[A/G]CAAGAAATAAATACA | 8924 |
rs61754656 | snp | A/C | 0.0020843 | 0.032215 | missense, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28272286 | TTTGCAGCAAGGGCA[A/C]AAGTGGGGCGCTGGT | 8924 |
rs61754657 | snp | C/T | 0.0265686 | 0.112154 | missense | HERC2 | GRCh38.p7 | 15:28168494 | ATTCATGGGACTAGC[C/T]ATCGCAGATGCGTCG | 8924 |
rs61754658 | snp | C/T | 0.00253631 | 0.0355207 | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28260840 | TGGCAATGCTGCAGG[C/T]TCTGGCTTGGTCACG | 8924 |
rs61754659 | snp | C/T | 0.000438463 | 0.0148 | synonymous-codon, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28257244 | GGACCACTCAGAACA[C/T]GATGACCAAGCAAAG | 8924 |
rs61755660 | snp | A/T | 1.67815e-05 | 0.00289663 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28233229 | AATTTAAACTTAGAC[A/T]TTATAGAGAGGTCAT | 8924 |
rs61755661 | snp | A/C | | | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28198391 | ACCTTTCACAACCCC[A/C]ACACTCTGATGAGTC | 8924 |
rs61755662 | snp | A/G | 0.000184429 | 0.00960107 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28192142 | CGGCCACAAAATACC[A/G]CAGACTGACCTATTT | 8924 |
rs61755663 | snp | C/T | 0.00261717 | 0.0360796 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28182440 | CTGGTCCTTGTCATT[C/T]AGGCCCCACACAAAC | 8924 |
rs61756151 | snp | A/G | 0.0110014 | 0.0733462 | synonymous-codon | HERC2 | GRCh38.p7 | 15:28130553 | AGAAAACTGGGATCC[A/G]CATTCCACTTTAACT | 8924 |
rs61756152 | snp | A/G | 0.223187 | 0.248558 | synonymous-codon | HERC2 | GRCh38.p7 | 15:28167726 | TGCAATGATGCTTGC[A/G]GCTCCCAGGTCATCC | 8924 |
rs61756153 | snp | C/T | 0.183159 | 0.240899 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28177463 | GTCACCTTCGCCCCA[C/T]GAAAACACTTTTCCA | 8924 |
rs61756154 | snp | A/C/G | 0.0141519 | 0.0829218 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28177481 | AAACACTTTTCCATC[A/C/G]ACAGTTAAAGCCGTC | 8924 |
rs61756155 | snp | C/G/T | 1.65173e-05 | 0.00287374 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28198433 | TTTGTATTTTGGTGT[C/G/T]GTGACAGAGGCTTTG | 8924 |
rs61756156 | snp | C/G | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28198485 | TTGATGTGAGAAGAA[C/G]AACTTGGTGGAGGAT | 8924 |
rs61756157 | snp | A/T | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28198487 | GATGTGAGAAGAAGA[A/T]CTTGGTGGAGGATAG | 8924 |
rs61756158 | snp | C/T | 8.2373e-05 | 0.00641714 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28201497 | CATAATCATCATTAC[C/T]CAAGAAATCAGCTCG | 8924 |
rs61756159 | snp | G/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28201513 | CAAGAAATCAGCTCG[G/T]TTTTTGTACGTCTGG | 8924 |
rs61757160 | snp | C/T | 0.0547768 | 0.156166 | synonymous-codon, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28233177 | TTCTCGAATTATCTT[C/T]TGAGCTATCCTCCTC | 8924 |
rs61757161 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28255978 | CGACCTGGACTTATG[C/T]TCACTTCATTGCCTG | 8924 |
rs61757226 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28272368 | CTGAAGCAACAACAG[C/G]ATGGCAGACAACATT | 8924 |
rs62007495 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | HERC2 | GRCh38.p7 | 15:28112211 | AATTCCTAGAACTTG[C/G]AGTAAGAAACAGCAC | 8924 |
rs62007543 | snp | A/G | 0.32955 | 0.237006 | intron-variant | HERC2 | GRCh38.p7 | 15:28119443 | AAAAAAAAAAGGCCT[A/G]ATATAAGTTGTCGTT | 8924 |
rs62007544 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28135278 | TTGACTTTTTTTTCC[C/T]TCTCAACAGAGGAAT | 8924 |
rs62008727 | snp | G/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28154816 | ACATGTGCACAACGT[G/T]CAGGTTTGTTACATA | 8924 |
rs62008728 | snp | A/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28162743 | AAATACAAAAAAAAT[A/T]AGCCGGGCATGGTGG | 8924 |
rs62008729 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | HERC2 | GRCh38.p7 | 15:28173140 | GGACCTCTGGAACAT[C/T]CACTTTGCAAAACAG | 8924 |
rs62008730 | snp | C/G | 0.0118322 | 0.0760005 | intron-variant | HERC2 | GRCh38.p7 | 15:28233634 | GGAATCTGCAGTGTA[C/G]CTAAAGTACACAGAT | 8924 |
rs62008731 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28272131 | CCAGAGAAAAACACT[A/G]CCGTTGACATGCATG | 8924 |
rs62008732 | snp | A/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28277482 | AAAAAAAAAAAAGGG[A/G]CTTTTTTAAAATTTT | 8924 |
rs62008733 | snp | A/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28278114 | AAAAAAAAAAAAAAT[A/T]GGCCAGGTATGGTGG | 8924 |
rs62008738 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28314862 | CAAGACTCCCTCTCA[A/G]GAAAAAAAAAAAAAA | 8924 |
rs62008743 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28322721 | CAATATAGGCCGGGC[A/G]TGGTGGCTCACGTAT | 8924 |
rs62996161 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28192941 | TTCCCTTTTTTTTTT[C/T]CCAACAGATTGCAAC | 8924 |
rs66823605 | in-del | -/G | | | intron-variant | HERC2 | GRCh38.p7 | 15:28136335 | GCACTGACATAATAT[-/G]AAGGAAGCCACAAGG | 8924 |
rs67813649 | in-del | -/A | | | intron-variant | HERC2 | GRCh38.p7 | 15:28291935 | AAAAAAAAAAAAAAA[-/A]GAGGCAAAAGGGCCA | 8924 |
rs71132834 | in-del | -/AA | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28129797 | GAGCAAGACTGTCTC[-/AA]AAAAAAAAAAAAAAA | 8924 |
rs71132835 | in-del | -/A | 0.373397 | 0.217424 | intron-variant | HERC2 | GRCh38.p7 | 15:28134704 | AAAAAAAAAAAAAAA[-/A]GAGGAAAAAATAATT | 8924 |
rs71132836 | in-del | -/T | 0.134802 | 0.221877 | intron-variant | HERC2 | GRCh38.p7 | 15:28136118 | AAAAAGGTGTTTTTT[-/T]CCCTTGTGGTTTATA | 8924 |
rs71132838 | in-del | -/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28206861 | ACCACGCCCAGTTAA[-/T]TTTTTTTTTTTTTTT | 8924 |
rs71132839 | in-del | -/A | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28209941 | GTGAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA | 8924 |
rs71132840 | in-del | -/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28224148 | TGTGTGTGTGTGTGG[-/T]GTGTGTGTGTGTGTA | 8924 |
rs71132842 | in-del | -/TGTGTGTGTGTGTGTA | 0 | 0 | | | GRCh38.p7 | 15:28245566 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTA]TATATTTTTTTTTTT | 8924 |
rs71132843 | in-del | -/A | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28247445 | GTGAAACTCGGTCTC[-/A]AAAAAAAAAAAAAAA | 8924 |
rs71132854 | in-del | -/T | 0 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28311103 | CCCTTGGTAATAGCC[-/T]TTTTTTTTTTTTTTT | 8924 |
rs71285051 | in-del | -/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28184228 | CATACATATATGTGT[-/G]GTATATATATGTGTG | 8924 |
rs71397290 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HERC2 | GRCh38.p7 | 15:28224015 | AAATGCAACTTTTGG[A/T]TGCTAATGAGGCCTC | 8924 |
rs71460406 | in-del | -/C | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28141212 | TTGCTCTTGTTGCCC[-/C]AGGCTGGAGTGCAAT | 8924 |
rs71467322 | snp | C/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28134505 | GCACAATGTTGAAGA[C/G]AAGTGGTGATAGCAG | 8924 |
rs71467323 | snp | G/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28181852 | GTGCAAGCTTCATGG[G/T]TTACTGACAAGGTGA | 8924 |
rs71467324 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28193940 | AGGCAGGAGAAAAAC[A/G]GTATAGATGGAAAAT | 8924 |
rs71467325 | snp | C/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28218405 | GGAATCCACACACAT[C/T]CACACCCACCCACAT | 8924 |
rs71467326 | snp | C/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28256601 | CCCCGCGCCAACAAT[C/T]TGCACCAAACACAGA | 8924 |
rs71467327 | snp | A/C | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28256621 | CCAAACACAGAAATA[A/C]CAGCTACAACTCAAC | 8924 |
rs71467328 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HERC2 | GRCh38.p7 | 15:28273083 | ACACTAACACATTTA[C/T]TACACGCTCCCTCCA | 8924 |
rs71467329 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28280205 | GAGTCGCAGGGCTGA[A/G]AGGGTGGTGGTGGCT | 8924 |
rs71859105 | in-del | -/A | 0.27278 | 0.24896 | intron-variant | HERC2, LOC107987422 | GRCh38.p7 | 15:28320477 | TACCTGTTTAAAAAG[-/A]AAAAAAAAATTAGGA | 8924 |
rs72018801 | in-del | -/TGCAGGGAGCACGTGCACCGCCCCACG | | | intron-variant | HERC2 | GRCh38.p7 | 15:28205286 | TCTCCCAGCATGACT[-/TGCAGGGAGCACGTGCACCGCCCCACG]GCTCTCAAGTTGCTC | 8924 |
rs72036273 | in-del | -/T | 0.366679 | 0.221102 | intron-variant | HERC2 | GRCh38.p7 | 15:28190011 | TTTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTG | 8924 |
rs72154154 | in-del | -/TTTT | 0.0222165 | 0.103028 | intron-variant | HERC2 | GRCh38.p7 | 15:28179235 | TTATCTACAACAGAA[-/TTTT]TTTAACAAAAAAAAA | 8924 |
rs72332871 | in-del | -/AGTGTTTGTAA | 0.439502 | 0.163061 | intron-variant | HERC2 | GRCh38.p7 | 15:28262670 | CTGCCACAGAAAGTC[-/AGTGTTTGTAA]AACTCAACAGGTTTA | 8924 |
rs72714137 | snp | A/G | 0.00253414 | 0.0355056 | intron-variant | HERC2 | GRCh38.p7 | 15:28144025 | AAGTATCAGAAGTCT[A/G]ATGGTTTCTTCCAAG | 8924 |
rs72714139 | snp | A/C | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28147426 | TTGAGCTCAGGAGTT[A/C]AAGACAGGCCTGGAC | 8924 |
rs72714140 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28166535 | GGTTTCCAAATCCTA[A/C]AAGCCACTAGCAGGA | 8924 |
rs72714141 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | HERC2 | GRCh38.p7 | 15:28174144 | ATTAGGAGTCCTGTT[C/T]ACACAGAAGGACAGC | 8924 |
rs72714142 | snp | A/C | 0.284471 | 0.247612 | intron-variant | HERC2 | GRCh38.p7 | 15:28181669 | AGACACTAAGTAATA[A/C]AAGGAATGCTGAATT | 8924 |
rs72714143 | snp | A/G | 0.223371 | 0.248578 | intron-variant | HERC2 | GRCh38.p7 | 15:28191915 | AATGTACAAGGCAAA[A/G]CCATCGGTGTGAAAG | 8924 |
rs72714145 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HERC2 | GRCh38.p7 | 15:28220289 | CCACACACCTGCATC[A/G]GAGGTGCCTGGGAGC | 8924 |
rs72714146 | snp | A/G | 0.410061 | 0.192043 | intron-variant | HERC2 | GRCh38.p7 | 15:28227468 | ATCCAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAC | 8924 |
rs72714147 | snp | A/G | 0.218345 | 0.247988 | intron-variant | HERC2 | GRCh38.p7 | 15:28233653 | AAGTACACAGATATC[A/G]AGCTCCTTACCTAAA | 8924 |
rs72714148 | snp | A/T | 0.491885 | 0.0631791 | intron-variant | HERC2 | GRCh38.p7 | 15:28240063 | TGTAGGGTTTTTTTT[A/T]AAATCCTTATCATTA | 8924 |
rs72714149 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HERC2 | GRCh38.p7 | 15:28249951 | TGAGCCACCACGCCC[A/G]GCCTAAGGAAACTAA | 8924 |
rs72714151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28281770 | GAAAGGTAAAGCAGT[A/G]CCCCTGCCCTTCTCA | 8924 |
rs73362603 | snp | C/G | 0.162253 | 0.234095 | intron-variant | HERC2 | GRCh38.p7 | 15:28177325 | AACCATTTCTATAAT[C/G]TATTCTATTCTAATT | 8924 |
rs73362604 | snp | A/C | 0.0156382 | 0.087032 | intron-variant | HERC2 | GRCh38.p7 | 15:28177538 | AGACACACGGATTGC[A/C]AAAGGGCAGGGAACA | 8924 |
rs73362608 | snp | A/T | 0.43088 | 0.172575 | intron-variant | HERC2 | GRCh38.p7 | 15:28182655 | TTTGCTTTAATAGAA[A/T]AAAACCTCAAGCATG | 8924 |
rs73362609 | snp | A/G | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28182824 | CGTGAACATGGGTGG[A/G]AATCATTCCAAGCCA | 8924 |
rs73362613 | snp | A/C | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28184961 | ACCCACCCCTACAAT[A/C]TATAATCCTTTTATT | 8924 |
rs73362615 | snp | C/G | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28185406 | AATCCAAAGCGCCTT[C/G]GGAATGTTAACAACA | 8924 |
rs73362621 | snp | A/T | 0.000560113 | 0.0167255 | intron-variant | HERC2 | GRCh38.p7 | 15:28191128 | CTTTTTAGGTAAACT[A/T]ACTGAATTACCTGAC | 8924 |
rs73362627 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | HERC2 | GRCh38.p7 | 15:28195523 | ATTAAAAAGGATGAC[A/G]TTCTGACACATGCTA | 8924 |
rs73362642 | snp | A/G | 0.161596 | 0.233848 | intron-variant | HERC2 | GRCh38.p7 | 15:28206961 | GGTTGCAGCGAGCCA[A/G]TATCACACCACCATA | 8924 |
rs73362648 | snp | C/T | 0.0648419 | 0.167978 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214357 | CCCACCTCTAAGTGA[C/T]GGCACTGCGCCGCTC | 8924 |
rs73362649 | snp | C/G | 0.0150012 | 0.085297 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214830 | AATTTATAACGACAA[C/G]CATTAAAAAAAATCT | 8924 |
rs73362650 | snp | C/G | 0.166506 | 0.235645 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214936 | GGAGTGCAGTGGCAC[C/G]GTCTCGGCTCACTAC | 8924 |
rs73362658 | snp | A/G | 0.442926 | 0.158996 | intron-variant | HERC2 | GRCh38.p7 | 15:28223747 | ATATTATATGCTTAT[A/G]ATTTCTTAAATGACA | 8924 |
rs73362700 | snp | C/T | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28282976 | CAGGAAGGGATGGGA[C/T]GGGACGGGACTGGAT | 8924 |
rs73362701 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | HERC2 | GRCh38.p7 | 15:28284061 | TACAGCATGCTTAAT[A/G]ATTTTGTGCATGAAA | 8924 |
rs73364703 | snp | A/T | 0.165853 | 0.235413 | intron-variant | HERC2 | GRCh38.p7 | 15:28284074 | ATAATTTTGTGCATG[A/T]AACAAAGTTCGTGCT | 8924 |
rs73364714 | snp | A/G | 0.16618 | 0.23553 | intron-variant | HERC2 | GRCh38.p7 | 15:28287985 | CACCTCAGCCTCCCA[A/G]AGTGCTGGGATTAGG | 8924 |
rs73364718 | snp | A/C | 0.167484 | 0.23599 | intron-variant | HERC2 | GRCh38.p7 | 15:28291388 | AGATACCATGGCAGG[A/C]GTCACAAATTATTTT | 8924 |
rs73379627 | snp | C/T | 0.158962 | 0.232835 | intron-variant | HERC2 | GRCh38.p7 | 15:28114287 | GCAGCCTGGAGGGGG[C/T]TGAGACAGCCCCAGA | 8924 |
rs73379637 | snp | C/T | 0.15698 | 0.23205 | intron-variant | HERC2 | GRCh38.p7 | 15:28121859 | ACAGCAGCCACGGGC[C/T]AGGGAGCACCGCGGA | 8924 |
rs73379639 | snp | C/T | 0.158302 | 0.232576 | intron-variant | HERC2 | GRCh38.p7 | 15:28122183 | GTGAAGACAGCAGGG[C/T]GTGGCCAAACATCAG | 8924 |
rs73379641 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | HERC2 | GRCh38.p7 | 15:28127661 | CCAGGGCTCCTTGGA[A/G]AAATGGCCAGGTCGA | 8924 |
rs73379643 | snp | C/T | 0.158302 | 0.232576 | intron-variant | HERC2 | GRCh38.p7 | 15:28129562 | ACAGGGGATCCCTCC[C/T]GAAACCCAGGTTCCC | 8924 |
rs73379651 | snp | C/G | 0.158962 | 0.232835 | intron-variant | HERC2 | GRCh38.p7 | 15:28136666 | TCAGGCCCATCATTT[C/G]TTTCTGTAAATGAAG | 8924 |
rs73379655 | snp | A/G | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28139532 | TCTGAGCTGGAGGAC[A/G]GAGCTATGCTGCATC | 8924 |
rs73379656 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HERC2 | GRCh38.p7 | 15:28140679 | GGCACATGTCACTGA[A/G]CCTGGCTTATTTTTG | 8924 |
rs73379659 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28147347 | AAAAATGCTTTTCTG[A/G]GCCAGATGTAGTGGT | 8924 |
rs73379661 | snp | C/T | 0.241914 | 0.249869 | intron-variant | HERC2 | GRCh38.p7 | 15:28149105 | CCAAGAACAGCCACA[C/T]GAACGTATAATCTAG | 8924 |
rs73379662 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | HERC2 | GRCh38.p7 | 15:28149173 | GAACATCACCAAGAA[C/T]GGCCACACGAACGCA | 8924 |
rs73379663 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | HERC2 | GRCh38.p7 | 15:28149293 | TACCGAAAAAACACA[C/T]GCAGCTCCTGAGAAC | 8924 |
rs73379664 | snp | A/G | 0.158632 | 0.232706 | intron-variant | HERC2 | GRCh38.p7 | 15:28149683 | ATGCAACTTCTAACC[A/G]AGAACATCACTTAGA | 8924 |
rs73379676 | snp | C/T | 0.05373 | 0.154849 | intron-variant | HERC2 | GRCh38.p7 | 15:28175468 | GACCCCCACGTCCCC[C/T]AAGTCAGGATGGCAC | 8924 |
rs74005605 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HERC2 | GRCh38.p7 | 15:28123717 | GGCCAGGCAGGCAGA[A/G]AAGGACCGCAGGAAC | 8924 |
rs74005609 | snp | C/T | 0.170084 | 0.236883 | intron-variant | HERC2 | GRCh38.p7 | 15:28136419 | AAAGCCAGCTTCTGG[C/T]GGGGAGGGTGTGAGG | 8924 |
rs74005616 | snp | C/T | 0.10237 | 0.201756 | intron-variant | HERC2 | GRCh38.p7 | 15:28148890 | CCACACAAACGTATA[C/T]TCTAGTAAAATTACT | 8924 |
rs74005617 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HERC2 | GRCh38.p7 | 15:28148939 | TAACTGAAACATCAC[C/T]GAGAACGGCCACACC | 8924 |
rs74005631 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HERC2 | GRCh38.p7 | 15:28149754 | AACACACGCGACTTC[C/T]AACCAAGAACGGTCA | 8924 |
rs74005643 | snp | C/T | 0.159951 | 0.233219 | intron-variant | HERC2 | GRCh38.p7 | 15:28195965 | TTGAGATTCTTTTAA[C/T]GTTTCTTTATGGAAA | 8924 |
rs74005645 | snp | A/C/G/T | 0.199622 | 0.244951 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28202136 | AGGCGGCATCATCCA[A/C/G/T]GTCCTCCACCACCTC | 8924 |
rs74005646 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | HERC2 | GRCh38.p7 | 15:28205023 | AATTTCAAGGAGGAC[A/G]GTGGGGTGGGCGGGG | 8924 |
rs74005655 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HERC2 | GRCh38.p7 | 15:28255061 | ACCAGAAAGCCTGGG[C/T]GTGGTCGCTCATGCT | 8924 |
rs74005657 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HERC2 | GRCh38.p7 | 15:28268216 | GATGCAGTTTGAGTA[A/G]ATAGAAGGCTGGCCA | 8924 |
rs74006708 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28289040 | AGAGCACTGCCCCGC[A/G]GCTCAGGCAGTGTAA | 8924 |
rs74007958 | snp | A/G | 0.0314426 | 0.121378 | intron-variant | HERC2 | GRCh38.p7 | 15:28116883 | GAGAAGCAGCCACTC[A/G]AAGTCCCCTCACACA | 8924 |
rs74007959 | snp | C/T | 0.00620726 | 0.0553634 | intron-variant | HERC2 | GRCh38.p7 | 15:28117338 | CTCGACTGTGGACAC[C/T]CGAGACCGCTGCCTC | 8924 |
rs74214947 | snp | C/G/T | 0.0232847 | 0.105357 | intron-variant | HERC2 | GRCh38.p7 | 15:28147853 | CAAGATTGGGCAACA[C/G/T]AGAGAGACTCATCTC | 8924 |
rs74248672 | snp | A/C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28124566 | GCTGGCATGAACATT[A/C/T]AAGGTTCTTTTGAGA | 8924 |
rs74396007 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | HERC2 | GRCh38.p7 | 15:28277189 | AAGGTGGGGAGAGAA[C/G]ACGTGAATGTGGGTA | 8924 |
rs74400391 | snp | C/T | 0.263535 | 0.249633 | intron-variant | HERC2 | GRCh38.p7 | 15:28189213 | GCATGCAGGTTAGGT[C/T]AGGAGTTTTCCATTT | 8924 |
rs74401202 | snp | G/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28189442 | GTATTCGGTTACATT[G/T]CAATAAGTTACCAGT | 8924 |
rs74417197 | snp | C/T | 0.258288 | 0.249863 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28214998 | CCTTGCTTCAGCTTC[C/T]TGAGTAGCAGGGATT | 8924 |
rs74443526 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28215042 | ACCAAGCCCGGCTCA[A/T]TTTTTTTTGGATTTT | 8924 |
rs74447445 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HERC2 | GRCh38.p7 | 15:28252402 | AGACACCAATAGCCC[A/G]TGAAGCAGCCTCCTC | 8924 |
rs74458218 | snp | C/G | 0.084364 | 0.187256 | intron-variant | HERC2 | GRCh38.p7 | 15:28169961 | TGCTACAATAACTAC[C/G]TGTATTTTCTTACCC | 8924 |
rs74472794 | snp | C/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28275465 | GCGGGTGAAGCCCTG[C/T]GTGCTTGACCCACCC | 8924 |
rs74482075 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | HERC2, LOC107987422 | GRCh38.p7 | 15:28314326 | ATGAACTAAAGTGTT[A/G]ACACTCTGCTCAGCA | 8924 |
rs74482920 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HERC2 | GRCh38.p7 | 15:28293811 | TCAAGAGCACTGGGA[A/C]ACAAAGGAAAAGCTG | 8924 |
rs74517019 | snp | C/G | 0.000367175 | 0.0135445 | intron-variant | HERC2 | GRCh38.p7 | 15:28113710 | ACTTTACACTTCTGT[C/G]TTCAGTGACACTGAC | 8924 |
rs74542546 | snp | A/C | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28264023 | AACTTTGTCTTACAA[A/C]AAAAAAAAAAAAAAA | 8924 |
rs74593828 | snp | C/G | 0.00293029 | 0.0381649 | missense | HERC2 | GRCh38.p7 | 15:28111918 | TGCAGAAGTGGATGG[C/G]GTACTTGAGCTTCTC | 8924 |
rs74650431 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HERC2 | GRCh38.p7 | 15:28184485 | TAGCTTTTCTTTCGA[C/T]AATATATTCAATTAC | 8924 |
rs74697264 | snp | A/T | | | intron-variant | HERC2 | GRCh38.p7 | 15:28129416 | CCCAGGGTTTCCATC[A/T]GGGCTGATCACACAG | 8924 |
rs74698548 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28143078 | AAACTAAAAAAAAAA[A/G]GCTTATCAAAATTCT | 8924 |
rs74703236 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | HERC2 | GRCh38.p7 | 15:28301635 | AGCTCCCTTGTCTGG[A/C]AAAAAAAAAAAAGCC | 8924 |
rs74707290 | snp | C/T | 0.116838 | 0.211584 | intron-variant | HERC2 | GRCh38.p7 | 15:28154728 | TCTCTACTGAGAATG[C/T]GGGGATGTGCATGGC | 8924 |
rs74738851 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | HERC2 | GRCh38.p7 | 15:28259255 | GCACATCACCAAGCT[A/C]GACGAAATTTTTGTA | 8924 |
rs74747661 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HERC2 | GRCh38.p7 | 15:28169410 | GAGACATCTGATCAA[A/C/T]GAAAAGAAAAAAAAT | 8924 |
rs74755256 | snp | A/C | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28172095 | AAAAAAAAAAACCTA[A/C]ACAATACTGGGACTA | 8924 |
rs74789945 | snp | A/C | 0.0082862 | 0.0638313 | missense, nc-transcript-variant | HERC2 | GRCh38.p7 | 15:28202387 | AGCACCAGTGAGAGA[A/C]TTCAGGGCAAACTCG | 8924 |
rs74803129 | snp | A/C | | | intron-variant | HERC2 | GRCh38.p7 | 15:28186898 | ATCAACTGAGTTACT[A/C]AAAGTTAATGCAGCC | 8924 |
rs74825242 | snp | A/G | 0.000887527 | 0.021047 | intron-variant | HERC2 | GRCh38.p7 | 15:28176940 | AAGCAACAAAAATGC[A/G]TATAATCACCATTTT | 8924 |
rs74849607 | snp | A/C/T | 0.00557861 | 0.0525638 | intron-variant | HERC2 | GRCh38.p7 | 15:28308212 | TTTCCATCTTTTGTG[A/C/T]CTTCTTTAATGTCTT | 8924 |
rs74853090 | snp | A/G | 0.260504 | 0.249779 | intron-variant | HERC2 | GRCh38.p7 | 15:28296433 | AGCCAAAATCATGCC[A/G]CTACACTCCAGCCTG | 8924 |
rs74872915 | snp | A/G | 0.43088 | 0.172575 | intron-variant | HERC2 | GRCh38.p7 | 15:28155339 | ccctgaggaatcgcc[A/G]cactgtgttccgcag | 8924 |
rs74877971 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | HERC2 | GRCh38.p7 | 15:28263321 | TACTGAGCAAACGAA[A/G]TCTAGGTGACACTTG | 8924 |
rs74879108 | snp | A/C | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28292253 | AAAAAAAAAAAAAAA[A/C]CCAGGCAAAGTATTT | 8924 |
rs74919039 | snp | A/C | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28227483 | GAAAAAAAAAAAAAA[A/C]ACAAAAAATAGTGTT | 8924 |
rs74922801 | snp | A/C | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28199146 | AGTGAGACCCCATCT[A/C]AAAAAAAAAAAAGAA | 8924 |
rs74940492 | snp | G/T | 0.25912 | 0.249834 | intron-variant | HERC2 | GRCh38.p7 | 15:28283925 | CCAAATTTCAGATTT[G/T]TATCAGATTTAGGAA | 8924 |
rs74950057 | snp | C/G | 0.263809 | 0.249618 | intron-variant | HERC2 | GRCh38.p7 | 15:28210200 | GTGCAGTGGCGCCAT[C/G]TCGGCTCACTGTAAG | 8924 |
rs74962392 | snp | A/G | 0.5 | 0 | intron-variant | HERC2 | GRCh38.p7 | 15:28143079 | AACTAAAAAAAAAAA[A/G]CTTATCAAAATTCTC | 8924 |