Variant (rsID / SNP)

rs1370154

rs1370154 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTC1. Location: chromosome 15, position 35,082,225. Clinical significance in the table: Benign.

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Reference-table entries

ACTC1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:35082225
Cytoband: 15q14
HGVS: NM_005159.4(ACTC1):c.*388G>A
Allele change: Silent

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 11|Dilated cardiomyopathy 1R

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.