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Variant (rsID / SNP)

rs71579375

VCL

rs71579375 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,871,748. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

VCLConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:75871748
Cytoband
10q22.2
HGVS
NM_014000.3(VCL):c.2827C>G (p.Pro943Ala)
Allele change
Silent

Associated conditions / phenotypes

Cardiovascular phenotype|Cardiomyopathy|Primary familial dilated cardiomyopathy|Dilated cardiomyopathy 1W

Public references

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