CASC20
cancer susceptibility 20
Known Variants14 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62198536 | 20:6,405,614 | A/G | intergenic variant | — |
| rs6038492 | 20:6,410,905 | G/A | — | — |
| rs2326783 | 20:6,413,830 | C/G | — | — |
| rs6054232 | 20:6,415,824 | T/C | intergenic variant | — |
| rs6117282 | 20:6,457,261 | C/T | intron variant | — |
| rs13043446 | 20:6,464,877 | C/T | intron variant | — |
| rs17721822 | 20:6,469,596 | G/A | intron variant | — |
| rs6085576 | 20:6,472,709 | T/C | intron variant | — |
| rs6140009 | 20:6,473,054 | C/G | — | — |
| rs1330021 | 20:6,495,416 | A/C | — | — |
| rs6117308 | 20:6,498,027 | G/A | intron variant | — |
| rs2065201 | 20:6,502,591 | C/T | — | — |
| rs55678551 | 20:6,506,275 | C/G | — | — |
| rs6117319 | 20:6,507,838 | G/C | splice region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.