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Variant (rsID / SNP)

rs371401403

MYBPC3

rs371401403 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,357,547. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MYBPC3Uncertain significance
Clinical significance (as recorded)
Uncertain significance
Variant type
single nucleotide variant
Chromosome / position
11:47357547
Cytoband
11p11.2
HGVS
NM_000256.3(MYBPC3):c.2618C>A (p.Pro873His)
Allele change
Missense_P873H

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 4|Primary familial hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy|Cardiovascular phenotype|Cardiomyopathy

Public references

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