Variant (rsID / SNP)

rs546586969

rs546586969 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,889,229. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MYH7Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 14:23889229
Cytoband: 14q11.2
HGVS: NM_000257.4(MYH7):c.3551A>T (p.Gln1184Leu)
Allele change: Missense_Q1184L

Associated conditions / phenotypes

Hypertrophic 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.