Variant (rsID / SNP)
rs1047840
rs1047840 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EXO1. Location: chromosome 1, position 242,042,301. The table records no clinical significance for this variant.
Reference-table entries
EXO1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:242042301
- HGVS
- NM_006027.4,c.1765G>A,p.Glu589Lys
- Allele change
- Missense_E588K
Associated conditions / phenotypes
Squamous Cell Carcinoma|Glioblastoma|Prostate Cancer|Non-Alcoholic Fatty Liver Disease|Lung Cancer Susceptibility 1|Gastric Cancer|Suppressor of Tumorigenicity 3|Lung Cancer|Hepatocellular Carcinoma|Lung Cancer Susceptibility 3|Cervical Cancer|Liver Disease|Oral Cancer|Fatty Liver Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.