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Variant (rsID / SNP)

rs781036800

VCL

rs781036800 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,871,749. 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
Deletion
Chromosome / position
10:75871749
Cytoband
10q22.2
HGVS
NM_014000.3(VCL):c.2828_2829del (p.Pro943fs)

Associated conditions / phenotypes

Primary dilated cardiomyopathy|Hypertrophic cardiomyopathy 15|Dilated cardiomyopathy 1W

Public references

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