Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs201528612

VCL

rs201528612 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,849,796. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

VCLConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:75849796
Cytoband
10q22.2
HGVS
NM_014000.3(VCL):c.1192C>T (p.Pro398Ser)
Allele change
Missense_P398S

Associated conditions / phenotypes

Dilated cardiomyopathy 1W|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.