Variant (rsID / SNP)
rs371488302
rs371488302 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,359,343. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
MYBPC3Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:47359343
- Cytoband
- 11p11.2
- HGVS
- NM_000256.3(MYBPC3):c.2311G>A (p.Val771Met)
- Allele change
- Missense_V771M
Associated conditions / phenotypes
Primary familial hypertrophic cardiomyopathy|Primary dilated cardiomyopathy|Hypertrophic cardiomyopathy 4|Left ventricular noncompaction 10|Left ventricular noncompaction 10|Hypertrophic cardiomyopathy 4|Hypertrophic cardiomyopathy|Cardiomyopathy|Hypertrophic cardiomyopathy 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.