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Variant (rsID / SNP)

rs768049705

MYBPC3

rs768049705 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,362,756. 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
11:47362756
Cytoband
11p11.2
HGVS
NM_000256.3(MYBPC3):c.1830C>G (p.Asp610Glu)
Allele change
Missense_D610E

Associated conditions / phenotypes

Cardiovascular phenotype|Hypertrophic cardiomyopathy|Cardiomyopathy

Public references

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