Variant (rsID / SNP)

rs77679218

rs77679218 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH6. Location: chromosome 14, position 23,874,851. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MYH6Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:23874851
Cytoband: 14q11.2
HGVS: NM_002471.4(MYH6):c.330G>A (p.Ala110=)
Allele change: Synonymous_A110A

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 14|Cardiovascular phenotype|Cardiomyopathy

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.