Variant (rsID / SNP)

rs150415679

rs150415679 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH6. Location: chromosome 14, position 23,868,075. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MYH6Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 14:23868075
Cytoband: 14q11.2
HGVS: NM_002471.4(MYH6):c.1753G>A (p.Gly585Ser)
Allele change: Missense_G585S

Associated conditions / phenotypes

Cardiovascular phenotype|Hypertrophic cardiomyopathy 14|Hypertrophic cardiomyopathy 1|Atrial septal defect 3

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.