Variant (rsID / SNP)
rs3813867
rs3813867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2E1. Location: chromosome 10, position 135,339,605. Clinical significance in the table: no interpretation for the single variant.
Reference-table entries
- Clinical significance (as recorded)
- no interpretation for the single variant
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:135339605
- Cytoband
- 10q26.3
- HGVS
- NM_000773.3(CYP2E1):c.-1295G>C
Associated conditions / phenotypes
Mycobacterium Tuberculosis 1|Squamous Cell Carcinoma|Oral Cancer|Acute Leukemia|Liver Disease|Oral Leukoplakia|Leukoplakia|Alcoholic Liver Cirrhosis|Alcohol Use Disorder|Hypertension, Essential|Alcohol Dependence|Non-Alcoholic Fatty Liver Disease|Lung Cancer Susceptibility 1|Colorectal Cancer|Hepatitis B|Fatty Liver Disease|Liver Cirrhosis|Polycythemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.