Variant (rsID / SNP)

rs7904077

rs7904077 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,854,218. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

VCLBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:75854218
Cytoband: 10q22.2
HGVS: NM_014000.3(VCL):c.1542C>T (p.Val514=)
Allele change: Synonymous_V514V

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.