Variant (rsID / SNP)
rs71579379
rs71579379 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,874,667. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
VCLConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:75874667
- Cytoband
- 10q22.2
- HGVS
- NM_014000.3(VCL):c.3258+10A>T
- Allele change
- Silent
Associated conditions / phenotypes
Dilated cardiomyopathy 1W|Cardiomyopathy|Primary dilated cardiomyopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.