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Variant (rsID / SNP)

rs267606911

MYH7

rs267606911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,897,796. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

MYH7Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
14:23897796
Cytoband
14q11.2
HGVS
NM_000257.4(MYH7):c.1491G>T (p.Glu497Asp)
Allele change
Missense_E497D

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 1|Hypertrophic cardiomyopathy|Cardiovascular phenotype|Cardiomyopathy|Dilated cardiomyopathy 1S

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.