CASC17
cancer susceptibility 17
Known Variants20 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs8072254 | 17:69,107,816 | A/C | — | — |
| rs984434 | 17:69,108,127 | T/C | intron variant | — |
| rs1859961 | 17:69,108,655 | A/C | — | — |
| rs1859962 | 17:69,108,753 | G/C | — | — |
| rs7217073 | 17:69,110,923 | A/G | intron variant | — |
| rs9911515 | 17:69,115,358 | A/C | — | — |
| rs4793529 | 17:69,118,636 | T/C | intron variant | — |
| rs6501436 | 17:69,119,290 | G/A | intron variant | — |
| rs11654749 | 17:69,125,606 | G/T | intron variant | — |
| rs8074021 | 17:69,127,020 | C/T | — | — |
| rs9899619 | 17:69,128,089 | G/A | intron variant | — |
| rs4793531 | 17:69,133,307 | C/G | — | — |
| rs7216323 | 17:69,140,933 | C/G | intron variant | — |
| rs56206939 | 17:69,152,825 | A/C | intron variant | — |
| rs68181052 | 17:69,165,750 | T/C | intron variant | — |
| rs2367264 | 17:69,175,190 | A/C | — | — |
| rs72869461 | 17:69,178,447 | T/C | intron variant | — |
| rs7214479 | 17:69,190,949 | T/A | — | — |
| rs1008348 | 17:69,191,316 | G/C | — | — |
| rs6501449 | 17:69,192,845 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.