Variant (rsID / SNP)

rs148091079

rs148091079 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH6. Location: chromosome 14, position 23,871,692. 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: 14:23871692
Cytoband: 14q11.2
HGVS: NM_002471.4(MYH6):c.1122G>A (p.Ala374=)
Allele change: Synonymous_A374A

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.