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Variant (rsID / SNP)

rs397516157

MYH7

rs397516157 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,894,102. 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
14:23894102
Cytoband
14q11.2
HGVS
NM_000257.4(MYH7):c.2555T>C (p.Met852Thr)
Allele change
Missense_M852T

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 1|Hypertrophic cardiomyopathy

Public references

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