Variant (rsID / SNP)
rs4801861
rs4801861 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN12. Location: chromosome 19, position 39,224,413. The table records no clinical significance for this variant.
Reference-table entries
CAPN12Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:39224413
- HGVS
- NM_144691.4,c.1887T>C,p.Phe629Phe
- Allele change
- Synonymous_F629F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.