| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ERCC5, LOC126861834
+1 more (A761T +1 more) | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | BIVM-ERCC5, ERCC5
+1 more (R819W +1 more) | Single nucleotide variant (missense variant) | Xeroderma pigmentosum, group G +1 more | |
Click to view in NCBI Gene