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Variant (rsID / SNP)

rs397516063

MYBPC3

rs397516063 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,371,336. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MYBPC3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:47371336
Cytoband
11p11.2
HGVS
NM_000256.3(MYBPC3):c.643C>T (p.Arg215Cys)
Allele change
Missense_R215C

Associated conditions / phenotypes

Cardiovascular phenotype|Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 4|Cardiomyopathy|See cases

Public references

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