CASC18
cancer susceptibility 18
Known Variants10 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11112691 | 12:106,105,776 | T/G | intron variant | — |
| rs11611140 | 12:106,106,588 | A/C | — | — |
| rs11112695 | 12:106,106,925 | T/A | intron variant | — |
| rs66913103 | 12:106,107,250 | C/A | intron variant | — |
| rs61941504 | 12:106,107,314 | G/A | — | — |
| rs67051635 | 12:106,107,420 | C/T | intron variant | — |
| rs11611703 | 12:106,107,458 | A/C | — | — |
| rs10861487 | 12:106,107,626 | A/G | regulatory region variant | — |
| rs10219670 | 12:106,108,719 | C/A | intron variant | — |
| rs11112698 | 12:106,111,773 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.