Variant (rsID / SNP)
rs671
rs671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH2. Location: chromosome 12, position 112,241,766. Clinical significance in the table: drug response.
Reference-table entries
ALDH2Drug response
- Clinical significance (as recorded)
- drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:112241766
- Cytoband
- 12q24.12
- HGVS
- NM_000690.4(ALDH2):c.1510G>A (p.Glu504Lys)
- Allele change
- Missense_E504K
Associated conditions / phenotypes
Susceptibility to hangover|Esophageal cancer, alcohol-related, susceptibility to|Sublingual nitroglycerin, susceptibility to poor response to|Alcohol sensitivity, acute|Alcohol dependence|AMED syndrome, digenic|ethanol response - Toxicity
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.