CASC8
cancer susceptibility 8
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6983267 | 8:127,401,060 | T/G | intergenic variant | — |
| rs1452179513 | 8:128,303,758 | C/G | — | — |
| rs283720 | 8:128,309,965 | A/G | regulatory region variant | — |
| rs16902094 | 8:128,320,346 | A/G | regulatory region variant | — |
| rs445114 | 8:128,323,181 | T/C | intron variant | — |
| rs378854 | 8:128,323,819 | C/T | intron variant | — |
| rs144898130 | 8:128,324,075 | C/T | intron variant | — |
| rs62516012 | 8:128,335,526 | C/A | — | — |
| rs620861 | 8:128,335,673 | G/T | — | — |
| rs442889 | 8:128,337,278 | C/T | — | — |
| rs16902104 | 8:128,340,908 | C/G | — | — |
| rs672888 | 8:128,345,463 | A/G | intron variant | — |
| rs13281615 | 8:128,355,618 | A/G | intron variant | — |
| rs35112951 | 8:128,370,271 | G/A | intron variant | — |
| rs1562430 | 8:128,387,852 | T/G | — | — |
| rs2392780 | 8:128,388,025 | A/G | intron variant | — |
| rs10505477 | 8:128,407,443 | A/G | downstream gene variant | — |
| rs10505476 | 8:128,408,116 | C/T | regulatory region variant | — |
| rs10808555 | 8:128,409,511 | G/T | — | — |
| rs10808556 | 8:128,413,147 | C/T | regulatory region variant | — |
| rs7013278 | 8:128,414,892 | T/C | intron variant | — |
| rs4871788 | 8:128,421,785 | G/A | upstream gene variant | — |
| rs7837328 | 8:128,423,127 | A/G | upstream gene variant | — |
| rs7000448 | 8:128,441,170 | C/T | intron variant | — |
| rs56868629 | 8:128,444,786 | G/A | intron variant | — |
| rs77805476 | 8:128,444,956 | T/C | intron variant | — |
| rs6470517 | 8:128,460,404 | A/G | intron variant | — |
| rs144180000 | 8:128,473,815 | T/C | intron variant | — |
| rs921146 | 8:128,475,185 | G/A | — | — |
| rs7825118 | 8:128,475,817 | G/T | — | — |
| rs78311688 | 8:128,479,976 | T/C | — | association |
| rs6981424 | 8:128,483,096 | G/A | intron variant | — |
| rs1447295 | 8:128,485,038 | A/C | regulatory region variant | — |
| rs10109700 | 8:128,485,964 | A/G | intron variant | — |
| rs9297758 | 8:128,486,588 | G/A | intron variant | — |
| rs7836840 | 8:128,491,792 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.