Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1229984
rs1229984
Entrez Id: 125
Gene Symbol: ADH1B
ADH1B
CUI: C0699791
Disease:
Stomach Carcinoma
0.020 GeneticVariation BEFREE However, no significant relationship was measured between ADH1B Arg47His and gastric cancer risk. 28002588 2016
dbSNP: rs1229984
rs1229984
Entrez Id: 125
Gene Symbol: ADH1B
ADH1B
CUI: C0699791
Disease:
Stomach Carcinoma
0.020 GeneticVariation BEFREE A known functional SNP in ADH1B (rs1229984) was associated with alcohol intake (P-value = 0.04) but not GC risk. 22144473 2012
dbSNP: rs17033
rs17033
Entrez Id: 125
Gene Symbol: ADH1B
ADH1B
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE Genotype and allele frequency analysis of these SNPs revealed that G allele of rs17033 is a risk allele (A vs G: OR = 3.67, 95% CI = 1.54-8.75, p = 0.002) for GC. 29166882 2017
dbSNP: rs283411
rs283411
Entrez Id: 125;126
Gene Symbol: ADH1B;ADH1C
ADH1B;ADH1C
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE Two intronic variants, one in ADH1C (rs283411) and one in ALDH2 (rs16941667), also were associated with GC risk (OR(T v C) = 0.59; 95% CI = 0.38-0.91 and OR(T v C) = 1.34; 95% CI = 1.00-1.79, respectively). 22144473 2012