Variant (rsID / SNP)
rs698
rs698 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH1C. Location: chromosome 4, position 100,260,789. Clinical significance in the table: protective.
Reference-table entries
ADH1CProtective
- Clinical significance (as recorded)
- protective
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:100260789
- Cytoband
- 4q23
- HGVS
- NM_000669.5(ADH1C):c.1048A>G (p.Ile350Val)
- Allele change
- Missense_I350V
Associated conditions / phenotypes
Alcohol dependence
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.