Variant (rsID / SNP)
rs886043238
rs886043238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP7B. Location: chromosome 13, position 52,542,677. Clinical significance in the table: Pathogenic.
Reference-table entries
ATP7BPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Duplication
- Chromosome / position
- 13:52542677
- Cytoband
- 13q14.3
- HGVS
- NM_000053.4(ATP7B):c.1605_1609dup (p.Ile537fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.