Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs908832
rs908832
0.030 GeneticVariation BEFREE It was showed that A2M V1000I (odd ratio (OR) = 1.26, 95% confidence interval (CI) = 1.07-1.49, P = 0.007), rs908832 allele of ABCA2 (OR = 1.55, 95% CI = 1.12-2.16, P = 0.009), 2384G >A of CHAT (OR = 1.22, 95% CI = 1.00-1.49, P = 0.05) and Ser447Ter of LPL in the Northern-American population (OR = 0.56, 95% CI = 0.35-0.91, P = 0.02) were significantly associated with the risk of AD. 24039871

2013

dbSNP: rs908832
rs908832
0.030 GeneticVariation BEFREE Here we confirm the association of rs908832</span> with AD in a Western European population (n = 291, P = 0.008). 16752360

2006

dbSNP: rs908832
rs908832
0.030 GeneticVariation BEFREE Among the 45 SNPs we tested, one synonymous SNP (rs908832) was found significantly associated with AD in both samples. 15649702

2005

dbSNP: rs770030911
rs770030911
0.010 GeneticVariation BEFREE Our results showed that A2M V1000I polymorphism in German, Korean, Chinese, Spanish, Italian and Polish populations, rs90883 of ABCA2 gene in French, American, Swiss, Greek and Japanese populations, 2384G >A of CHAT gene in British and Korean populations and LPL Ser447Ter in the Northern-American population were associated with the risk of AD. 24039871

2013