Variant (rsID / SNP)

rs150574114

rs150574114 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH6. Location: chromosome 14, position 23,876,347. Clinical significance in the table: Benign.

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Reference-table entries

MYH6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:23876347
Cytoband: 14q11.2
HGVS: NM_002471.4(MYH6):c.86G>A (p.Arg29Gln)
Allele change: Missense_R29Q

Associated conditions / phenotypes

Cardiovascular phenotype|Hypertrophic cardiomyopathy 14|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.