Variant (rsID / SNP)
rs2031920
rs2031920 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2E1. Location: chromosome 10, position 135,339,845. 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
- 10:135339845
- Cytoband
- 10q26.3
- HGVS
- NM_000773.3(CYP2E1):c.-1055C>T
Associated conditions / phenotypes
Hepatocellular Carcinoma|Nasopharyngeal Carcinoma|Squamous Cell Carcinoma|Cardia Cancer|Gastric Cancer|Esophageal Cancer|Oral Cancer|Acute Leukemia|Mycobacterium Tuberculosis 1|Liver Disease|Oral Leukoplakia|Leukoplakia|Alcoholic Liver Cirrhosis|Alcohol Use Disorder|Hypertension, Essential|Alcohol Dependence|Bladder Cancer|Non-Alcoholic Fatty Liver Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.