Variant (rsID / SNP)
rs879255499
rs879255499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP7B. Location: chromosome 13, position 52,585,900. The table records no clinical significance for this variant.
Reference-table entries
ATP7BNot classified
- Variant type
- Deletion
- Chromosome / position
- 13:52585900
- Cytoband
- 13q14.3
- HGVS
- NM_001406512.1(ATP7B):c.-176_-162delCGAGGTGGCCGAGAC
Associated conditions / phenotypes
Wilson disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.