Variant (rsID / SNP)

rs148966602

rs148966602 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,830,566. 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: 10:75830566
Cytoband: 10q22.2
HGVS: NM_014000.3(VCL):c.378C>T (p.Phe126=)
Allele change: Synonymous_F126F

Associated conditions / phenotypes

Dilated cardiomyopathy 1W|Cardiomyopathy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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