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Variant (rsID / SNP)

rs1671064

ACTN3

rs1671064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTN3. Location: chromosome 11, position 66,327,673. The table records no clinical significance for this variant.

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Reference-table entries

ACTN3Not classified
Variant type
missense_variant
Chromosome / position
11:66327673
HGVS
NM_001258371.3,c.1697G>A,p.Arg566Gln
Allele change
Missense_R566Q

Associated conditions / phenotypes

Bruxism

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.