Variant (rsID / SNP)

rs532841

rs532841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DLC1. Location: chromosome 8, position 12,957,475. The table records no clinical significance for this variant.

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Reference-table entries

DLC1Not classified

Variant type: missense_variant
Chromosome / position: 8:12957475
HGVS: NM_001348081.2,c.2371G>A,p.Val791Met
Allele change: Missense_V791M

Associated conditions / phenotypes

Hepatocellular Carcinoma|Hepatitis B|Hepatitis|Liver Cirrhosis

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.