Variant (rsID / SNP)

rs111729952

rs111729952 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,359,347. Clinical significance in the table: Pathogenic.

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Reference-table entries

MYBPC3Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:47359347
Cytoband: 11p11.2
HGVS: NM_000256.3(MYBPC3):c.2309-2A>G
Allele change: Silent

Associated conditions / phenotypes

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

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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