Variant (rsID / SNP)

rs36212066

rs36212066 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,353,826. 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: Deletion
Chromosome / position: 11:47353826
Cytoband: 11p11.2
HGVS: NM_000256.3(MYBPC3):c.3628-41_3628-17del

Associated conditions / phenotypes

Left ventricular noncompaction 10|Hypertrophic cardiomyopathy|Cardiomyopathy|Hypertrophic cardiomyopathy 4

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.