Variant (rsID / SNP)
rs61823553
rs61823553 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN8. Location: chromosome 1, position 223,718,651. The table records no clinical significance for this variant.
Reference-table entries
CAPN8Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:223718651
- HGVS
- NM_001143962.2,c.1475C>T,p.Thr492Met
- Allele change
- Synonymous_N483N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
