| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs202276156 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396811 | TAAATTGAAAAAAAT[A/T]ATCATTGCTGTTCGT | 33035 |
| rs202291437 | snp | G/T | | | upstream-variant-2KB, missense, downstream-variant-500B | jb, Syx16, l(1)G0004, HERC2 | Release_6_plus_ISO1_MT | X:20392525 | TGACGCACATCTTGC[G/T]GTTCTTGCGCTGATA | 33035 |
| rs202292631 | snp | C/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393934 | AAGTGATTTTTTCAA[C/T]ATACGGATTGGATAG | 33035 |
| rs202302794 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397229 | GAGTCTAGCCAATGA[A/T]GAAGCTGTTATTGCT | 33035 |
| rs202446494 | snp | A/G | | | downstream-variant-500B | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412294 | ACGACTGAAAGAAAT[A/G]GATCCACCCGGGGGC | 33035 |
| rs202470269 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20411358 | AATGGCGACCGATTG[C/T]GTCCAACACTGATTC | 33035 |
| rs202603967 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397867 | GTTCGCTTAAGAGCA[C/T]GATGTCTATATTGCG | 33035 |
| rs202616486 | snp | C/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20398707 | GTAAGCTACCGCCAG[C/G]TACCCCGTTATCCTC | 33035 |
| rs202736502 | snp | G/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397126 | AGGTATGACTTCGAT[G/T]AGCAGGATGTGAAGC | 33035 |
| rs202742096 | snp | A/G | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393868 | TATTATTTTCTTATT[A/G]TCTGTAGAATCTGTA | 33035 |
| rs202837229 | snp | G/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396952 | TTTTTTTTTATTATT[G/T]AACTTACGGTAGGAA | 33035 |
| rs202848607 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412384 | TAGACTAAAAATTTA[A/G]CAGATCTCTTGAAGC | 33035 |
| rs202853554 | snp | A/G | | | synonymous-codon, downstream-variant-500B, upstream-variant-2KB | Syx16, l(1)G0004, HERC2 | Release_6_plus_ISO1_MT | X:20392820 | GTCGATGGCCTGCTC[A/G]TCGTCCTCGAACAGA | 33035 |
| rs202855805 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397768 | GCGCCTTGGCAGCCG[C/T]TATGCCGTGAGCTCG | 33035 |
| rs202880552 | snp | A/C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396855 | TCGTTTTACAGCCAT[A/C/T]ATATTGGTTATCGTA | 33035 |
| rs202904559 | snp | A/T | | | downstream-variant-500B | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412268 | CCCCCCGTTTAATTT[A/T]GTATCTTGCAACGAC | 33035 |
| rs202921177 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20398045 | AAGCATTTTGGTTGG[C/T]GAAGGCTGTGTGTGT | 33035 |
| rs203012046 | snp | A/G | | | intron-variant, upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393337 | CCCTGCGCATGGACT[A/G]CTGTTTGTTTACCCA | 33035 |
| rs203023848 | snp | A/C | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20394086 | AACGACCGTAATAGT[A/C]CAATAAAAGTATTCA | 33035 |
| rs203042182 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397897 | GCTTAGCCTCAGTCT[A/G]ACCTAGGAGTATGAT | 33035 |
| rs203066705 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397493 | TGTTTGCAGCATGTG[C/T]TGGTCCATTTCGGCA | 33035 |
| rs203140795 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397460 | CAACTATATCCAGTA[A/G]GTAAAGAGGGCGGTA | 33035 |
| rs203142137 | snp | A/C | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20394073 | CTTTTAGCAATAAAA[A/C]GACCGTAATAGTACA | 33035 |
| rs203162620 | snp | C/T | | | downstream-variant-500B, missense | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412497 | CCGCCTGCTCCTCCG[C/T]CTGCGGCTGGTCGTC | 33035 |
| rs203284556 | snp | A/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393972 | AGAAATATTCGGAAA[A/T]TACAGAATATAGTAT | 33035 |
| rs203444454 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396930 | GTGTAGCACGCTTTT[C/T]AGCGTATTTTTTTTT | 33035 |
| rs203445229 | snp | A/C | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397095 | GTCCTTGCACGCTCA[A/C]CGGGACTGTCAGTCA | 33035 |
| rs203446481 | snp | A/C | | | missense, upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393219 | GCACTCGTCGTCCCG[A/C]TGATCATCGAAGGCG | 33035 |
| rs203457832 | snp | A/C/G | | | downstream-variant-500B, missense, synonymous-codon | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412645 | GTCACGTTCATCCTC[A/C/G]TCCAGCTCATCCCGC | 33035 |
| rs203529227 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20399368 | TCATTGATCTTTTAC[C/T]TTAGGACGGATGGAG | 33035 |
| rs203567412 | snp | A/C | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397950 | GGGCGTGCATTATAG[A/C]TTATTTTAGGCTCGT | 33035 |
| rs203569939 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397016 | CGTAGGTGGCATGCA[C/T]GATTCATAATCCCTA | 33035 |
| rs203596526 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397328 | CTTTAGGGACTCTTG[A/G]GACAGAGACTAGCAT | 33035 |
| rs203601345 | snp | G/T | | | downstream-variant-500B, synonymous-codon | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412441 | TTCATCGCTGGTAAA[G/T]GACAGGCCGGAAGTG | 33035 |
| rs203703725 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20398096 | AGGAGTTATAAACCT[A/G]ATGCCCTTTTTTCCA | 33035 |
| rs203705989 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20402807 | TGGTATGTGTCCTTT[A/G]TGGTAGTAAAACAAC | 33035 |
| rs203738145 | snp | A/G | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393832 | CACCGTTACATGTCC[A/G]AGAATTATACTTATT | 33035 |
| rs203805803 | snp | A/C | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393758 | GCAGTGTGCCCGCTG[A/C]CTTGCTCGCCCAGAA | 33035 |
| rs203818709 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397047 | GTATAATTATTCCTA[C/T]CTGCTAAAACAAAAA | 33035 |
| rs203823330 | snp | C/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20394346 | AGAGCTATCGAAAGG[C/T]AAAACATATCGATGG | 33035 |
| rs203830434 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397727 | GAGGCACCAGGAATC[A/G]CTGTCTACGCTATCC | 33035 |
| rs203890310 | snp | A/T | | | downstream-variant-500B | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412251 | ACTTTATAAAGCAAT[A/T]GCCCCCCGTTTAATT | 33035 |
| rs203925943 | snp | A/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20394130 | TGCGTTCTCTTTTTT[A/T]GCGTTACGAAAGAGT | 33035 |
| rs204039263 | snp | C/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397783 | CTATGCCGTGAGCTC[C/G]ACCTGGTGGGTACTG | 33035 |
| rs204050388 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397369 | TTTTTCCTACTTCCT[A/G]CTTAGTAGAACTGCC | 33035 |
| rs204123234 | snp | A/G | | | upstream-variant-2KB, missense, downstream-variant-500B | jb, Syx16, l(1)G0004, HERC2 | Release_6_plus_ISO1_MT | X:20392644 | CCCTGCTCCTGGACC[A/G]TGTGGCCCAGGTCCT | 33035 |
| rs204130731 | snp | A/C | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393938 | GATTTTTTCAATATA[A/C]GGATTGGATAGCTCC | 33035 |
| rs204235624 | snp | C/T | | | intron-variant, upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393534 | AGTTGATGATAACAG[C/T]GAAGACCCCAGACGG | 33035 |
| rs204258831 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20411375 | TCCAACACTGATTCT[A/G]ATTAATCGCGAACCA | 33035 |
| rs204261062 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | jb, Syx16, l(1)G0004, HERC2 | Release_6_plus_ISO1_MT | X:20392481 | GAGCAGCAGCAGCAT[A/G]AAGAATGTGACCGCC | 33035 |
| rs204292956 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20402834 | CAACCATTTGAGTTT[A/G]AGTGGCTAACAATAA | 33035 |
| rs204307643 | snp | C/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397638 | GTTGGTCGTCATAGT[C/G]TGGTCTGCATTGGTG | 33035 |
| rs204392891 | snp | A/G | | | downstream-variant-500B | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412288 | CTTGCAACGACTGAA[A/G]GAAATGGATCCACCC | 33035 |
| rs204420440 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393009 | GCGGGAGTTCAGCTG[A/G]AGCAGGTAGGCATTC | 33035 |
| rs204431340 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396864 | AGCCATTATATTGGT[A/T]ATCGTACATATTATA | 33035 |
| rs204473505 | snp | A/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393973 | GAAATATTCGGAAAT[A/T]ACAGAATATAGTATT | 33035 |
| rs204491290 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397948 | ATGGGCGTGCATTAT[A/G]GCTTATTTTAGGCTC | 33035 |
| rs204505224 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20410565 | GAGGGATAACCGATA[A/G]TAATAACCGATCACT | 33035 |
| rs204554105 | snp | A/C | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397306 | GGTCTATCATAACAC[A/C]CAAGTACTTTAGGGA | 33035 |
| rs204583608 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396829 | CATTGCTGTTCGTCT[C/T]CACTGCTAGTTCGTT | 33035 |
| rs204622708 | snp | A/C | | | downstream-variant-500B | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412299 | TGAAAGAAATGGATC[A/C]ACCCGGGGGCGCCAA | 33035 |
| rs204629406 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412388 | CTAAAAATTTAGCAG[A/T]TCTCTTGAAGCCTAC | 33035 |
| rs204650158 | snp | A/C | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397953 | CGTGCATTATAGCTT[A/C]TTTTAGGCTCGTTCT | 33035 |
| rs204682024 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20400333 | AACTTGCAGAGCTAT[C/T]TTCGTCATAATTGCA | 33035 |
| rs204702066 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393452 | CTCCGCCTCGCGCAC[C/T]GAGTGCTTTAGAAGG | 33035 |
| rs204708204 | snp | G/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20394115 | CAATAATTTGTTATG[G/T]GCGTTCTCTTTTTTT | 33035 |
| rs204714981 | snp | G/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397885 | TGTCTATATTGCGCT[G/T]AGCCTCAGTCTGACC | 33035 |
| rs204729402 | snp | C/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20398743 | CTGTCATAACTTTTG[C/G]TTTTTCCTGCAGCAC | 33035 |
| rs204824409 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20402797 | GAGCCATATCTGGTA[A/T]GTGTCCTTTGTGGTA | 33035 |
| rs204849355 | snp | G/T | | | downstream-variant-500B, missense | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412508 | TCCGCCTGCGGCTGG[G/T]CGTCGGCCTGTTCCC | 33035 |
| rs204987116 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397148 | ATGTGAAGCCAGGTC[A/G]CAGCAAAGCCTTTGC | 33035 |
| rs204989119 | snp | C/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393900 | TTTATATGTATACTC[C/T]TAAACATCCTATTTG | 33035 |
| rs205083110 | snp | G/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397032 | GATTCATAATCCCTA[G/T]TATAATTATTCCTAT | 33035 |
| rs205087082 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393677 | TTTCTTGGGGATTGG[A/G]AGGATTGATCCAAGT | 33035 |
| rs205244733 | snp | G/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397683 | AGCCAGGACCCCAGT[G/T]TCAGATGGGGTTACA | 33035 |
| rs205256127 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20398103 | ATAAACCTGATGCCC[A/T]TTTTTCCAATTCGTT | 33035 |
| rs205267614 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20402820 | TTGTGGTAGTAAAAC[A/T]ACCATTTGAGTTTAA | 33035 |
| rs205301573 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396953 | TTTTTTTTATTATTG[A/G]ACTTACGGTAGGAAA | 33035 |
| rs205311242 | snp | A/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20394075 | TTTAGCAATAAAACG[A/T]CCGTAATAGTACAAT | 33035 |
| rs205318931 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397464 | TATATCCAGTAGGTA[A/T]AGAGGGCGGTAGCTG | 33035 |
| rs205319462 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397582 | CCTCGACGACTTCGA[A/G]ATCTGTGACGCACGG | 33035 |
| rs205322349 | snp | C/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393862 | TTTAAATATTATTTT[C/T]TTATTATCTGTAGAA | 33035 |
| rs205348522 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396932 | GTAGCACGCTTTTCA[A/G]CGTATTTTTTTTTAT | 33035 |
| rs205400829 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20393246 | GGCGGGTCGCAGGAG[A/G]TGGCGTGCGTGCAGG | 33035 |
| rs205414473 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20398062 | AAGGCTGTGTGTGTT[A/T]ACTTAACTTTAGAAT | 33035 |
| rs205422098 | snp | C/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397057 | TCCTATCTGCTAAAA[C/G]AAAAACCTCCGTGTG | 33035 |
| rs205432004 | snp | A/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20399369 | CATTGATCTTTTACC[A/T]TAGGACGGATGGAGT | 33035 |
| rs205441375 | snp | A/G | | | downstream-variant-500B | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412263 | AATTGCCCCCCGTTT[A/G]ATTTAGTATCTTGCA | 33035 |
| rs205495831 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | jb, Syx16, l(1)G0004, HERC2 | Release_6_plus_ISO1_MT | X:20392508 | CGCCGCCAGGACGAG[A/G]ATGACGCACATCTTG | 33035 |
| rs205504815 | snp | G/T | | | downstream-variant-500B, missense | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412490 | CTGTACTCCGCCTGC[G/T]CCTCCGCCTGCGGCT | 33035 |
| rs205631703 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20410577 | ATAGTAATAACCGAT[C/T]ACTAATTCCCTTGTT | 33035 |
| rs205874912 | snp | A/T | | | upstream-variant-2KB | Syx16, HERC2 | Release_6_plus_ISO1_MT | X:20394209 | AGGCTAATGTTTAAA[A/T]ATTACAAATTTACAG | 33035 |
| rs205990811 | snp | C/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397109 | ACCGGGACTGTCAGT[C/G]AAGGTATGACTTCGA | 33035 |
| rs205991669 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20396830 | ATTGCTGTTCGTCTT[C/T]ACTGCTAGTTCGTTT | 33035 |
| rs205998836 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397861 | TCCAAGGTTCGCTTA[A/G]GAGCACGATGTCTAT | 33035 |
| rs206000056 | snp | A/G | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397309 | CTATCATAACACCCA[A/G]GTACTTTAGGGACTC | 33035 |
| rs206011616 | snp | G/T | | | downstream-variant-500B, synonymous-codon | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412678 | GACTTCCACTGCGGC[G/T]GCCTGAGCTGGGGAA | 33035 |
| rs206028690 | snp | A/G | | | downstream-variant-500B, synonymous-codon | HERC2, CG15459 | Release_6_plus_ISO1_MT | X:20412438 | CTTTTCATCGCTGGT[A/G]AAGGACAGGCCGGAA | 33035 |
| rs206085081 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397758 | TGCAGCGACCGCGCC[C/T]TGGCAGCCGCTATGC | 33035 |
| rs206085804 | snp | C/T | | | intron-variant | HERC2 | Release_6_plus_ISO1_MT | X:20397890 | ATATTGCGCTTAGCC[C/T]CAGTCTGACCTAGGA | 33035 |