Variant (rsID / SNP)

rs2856655

rs2856655 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,359,085. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

MYBPC3Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:47359085
Cytoband: 11p11.2
HGVS: NM_000256.3(MYBPC3):c.2459G>A (p.Arg820Gln)
Allele change: Missense_R820Q

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 4|Hypertrophic cardiomyopathy|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.