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Variant (rsID / SNP)

rs150385900

VCL

rs150385900 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,867,074. 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
10:75867074
Cytoband
10q22.2
HGVS
NM_014000.3(VCL):c.2521G>C (p.Asp841His)
Allele change
Missense_D841H

Associated conditions / phenotypes

Cardiovascular phenotype|Dilated cardiomyopathy 1W|Cardiomyopathy

Public references

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