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Variant (rsID / SNP)

rs397516009

MYBPC3

rs397516009 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,354,846. 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
11:47354846
Cytoband
11p11.2
HGVS
NM_000256.3(MYBPC3):c.3229G>A (p.Ala1077Thr)
Allele change
Missense_A1077T

Associated conditions / phenotypes

Hypertrophic cardiomyopathy|Cardiomyopathy

Public references

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