Variant (rsID / SNP)
rs373514686
rs373514686 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,885,349. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
MYH7Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:23885349
- Cytoband
- 14q11.2
- HGVS
- NM_000257.4(MYH7):c.4817G>A (p.Arg1606His)
- Allele change
- Missense_R1606H
Associated conditions / phenotypes
Hypertrophic cardiomyopathy 1|Hypertrophic cardiomyopathy|Cardiovascular phenotype|Primary familial hypertrophic cardiomyopathy|Cardiomyopathy|Arrhythmogenic right ventricular cardiomyopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.