Variant (rsID / SNP)

rs137877092

rs137877092 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,855,541. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

VCLBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:75855541
Cytoband: 10q22.2
HGVS: NM_014000.3(VCL):c.1671C>T (p.Asp557=)
Allele change: Synonymous_D557D

Associated conditions / phenotypes

Cardiovascular phenotype|Cardiomyopathy|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.