Variant (rsID / SNP)
rs2066702
rs2066702 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH1B. Location: chromosome 4, position 100,229,017. Clinical significance in the table: protective.
Reference-table entries
ADH1BProtective
- Clinical significance (as recorded)
- protective
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:100229017
- Cytoband
- 4q23
- HGVS
- NM_000668.6(ADH1B):c.1108C>T (p.Arg370Cys)
- Allele change
- Missense_R330C
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.