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Variant (rsID / SNP)

rs397516039

MYBPC3

rs397516039 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,353,684. 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
single nucleotide variant
Chromosome / position
11:47353684
Cytoband
11p11.2
HGVS
NM_000256.3(MYBPC3):c.3753T>C (p.Tyr1251=)
Allele change
Nonsense_Y1251X

Associated conditions / phenotypes

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

Public references

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