Variant (rsID / SNP)

rs1229984

rs1229984 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH1B. Location: chromosome 4, position 100,239,319. Clinical significance in the table: protective.

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Reference-table entries

ADH1BProtective

Clinical significance (as recorded): protective
Variant type: single nucleotide variant
Chromosome / position: 4:100239319
Cytoband: 4q23
HGVS: NM_000668.5(ADH1B):c.143A= (p.His48=)
Allele change: Missense_H8R

Associated conditions / phenotypes

Alcohol dependence|Aerodigestive tract cancer, squamous cell, alcohol-related, protection against

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.