Variant (rsID / SNP)

rs12586591

rs12586591 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTN1. Location: chromosome 14, position 69,345,647. The table records no clinical significance for this variant.

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Reference-table entries

ACTN1Not classified

Variant type: intron_variant
Chromosome / position: 14:69345647
HGVS: NM_001130004.2,c.2361+59G>A
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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