Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11731003
rs11731003
SORCS2
T 0.700 GeneticVariation GWASCAT Risk Locus Identification Ties Alcohol Withdrawal Symptoms to SORCS2. 30252935

2018
dbSNP: rs1806201
rs1806201
GRIN2B
0.010 GeneticVariation BEFREE The associations of GRIN2B polymorphism (rs1806201) with alcohol withdrawal and related clinical parameters in alcohol dependent subjects were investigated. 26771436

2017
dbSNP: rs1390938
rs1390938
SLC18A1
0.010 GeneticVariation BEFREE This study shows that genetic variants in VMAT1, including the functional SNP rs1390938, contribute to the severity of AW in patients of European descent. 26876819

2016
dbSNP: rs371308207
rs371308207
C1D
0.010 GeneticVariation BEFREE The A/A genotype in exon 8 A/G polymorphism seems to be a positive predictive factor for the presence or the lack of seizures in a</span>lcohol withdrawal syndrome. 23238469

2012
dbSNP: rs1258159645
rs1258159645
NQO1
0.010 GeneticVariation BEFREE Moreover, GSTM1 gene deletion and missense mutation (Pro187Ser) of the NQO1 gene showed no significant association with alcohol withdrawal symptoms. 12960511

2003
dbSNP: rs1800566
rs1800566
NQO1
0.010 GeneticVariation BEFREE Moreover, GSTM1 gene deletion and missense mutation (Pro187Ser) of the NQO1 gene showed no significant association with alcohol withdrawal symptoms. 12960511

2003