Variant (rsID / SNP)

rs146278697

rs146278697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,849,841. Clinical significance in the table: Likely benign.

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Reference-table entries

VCLLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:75849841
Cytoband: 10q22.2
HGVS: NM_014000.3(VCL):c.1237G>A (p.Ala413Thr)
Allele change: Missense_A413T

Associated conditions / phenotypes

Cardiovascular phenotype|Dilated cardiomyopathy 1W

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.