| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193338496 | snp | A/G | 0.0584834 | 0.16069 | synonymous-codon | drh-1 | WS195 | IV:6608519 | CTTGATGACAAGACT[A/G]CATTCAGGAACATCC | 177425 |
| rs193338497 | snp | A/T | 0.0768 | 0.180282 | missense | drh-1 | WS195 | IV:6608592 | TCTCCATCAGCAAAC[A/T]TTTTCAACTTTTCCA | 177425 |
| rs193338498 | snp | C/T | 0.0198 | 0.0975088 | synonymous-codon | drh-1 | WS195 | IV:6608651 | GGCGCTGCTCGCAGT[C/T]GACTTGTTCAATCCT | 177425 |
| rs193338499 | snp | C/T | 0.0198 | 0.0975088 | intron-variant | drh-1 | WS195 | IV:6608685 | ATAAAAATGAATAAG[C/T]TATGTTTTCAAAACG | 177425 |
| rs193338500 | snp | C/T | 0.0771698 | 0.180637 | intron-variant | drh-1 | WS195 | IV:6608693 | GAATAAGTTATGTTT[C/T]CAAAACGAATAACTC | 177425 |
| rs193338501 | snp | A/C | 0.0582 | 0.160352 | missense | drh-1 | WS195 | IV:6608740 | AGATTTGATTCCAAG[A/C]ATCAGCAATTCTTCG | 177425 |
| rs193338502 | snp | A/G | 0.0198 | 0.0975088 | intron-variant | drh-1 | WS195 | IV:6609094 | TACAGAAACATTCCT[A/G]GAATCGAATTCAGAA | 177425 |
| rs193338503 | snp | A/C | 0.0198 | 0.0975088 | intron-variant | drh-1 | WS195 | IV:6609099 | AAACATTCCTGGAAT[A/C]GAATTCAGAATAGTT | 177425 |
| rs193338504 | snp | A/C | 0.0205106 | 0.0991697 | missense | drh-1 | WS195 | IV:6611223 | GTAGTGGTATTCTCT[A/C]ATAATATCTGAAAAT | 177425 |
| rs193338505 | snp | C/T | 0.0582 | 0.160352 | intron-variant | drh-1 | WS195 | IV:6612039 | ATCATTCTGAAAAAT[C/T]AGTTATTAAGAATGA | 177425 |
| rs193338506 | snp | G/T | 0.0768 | 0.180282 | intron-variant | drh-1 | WS195 | IV:6612041 | CATTCTGAAAAATTA[G/T]TTATTAAGAATGAAT | 177425 |