Variant (rsID / SNP)
rs540874
rs540874 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTN3. Location: chromosome 11, position 66,329,732. The table records no clinical significance for this variant.
Reference-table entries
ACTN3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:66329732
- HGVS
- NM_001258371.3,c.2456A>G,p.Gln819Arg
- Allele change
- Missense_Q819R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
