Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs231779
rs231779
CTLA4
0.030 GeneticVariation BEFREE Interactions among the SNPs of rs231775, rs231779 and rs3087243 significantly increase the susceptibility to GD. 30223781

2018
dbSNP: rs231779
rs231779
CTLA4
0.030 GeneticVariation BEFREE Moreover, the logistic regression analysis in the combined Chinese Han cohort revealed that SNP rs231779 (allele frequencies p = 2.81x10(-9), OR = 1.35, and genotype distributions p = 2.75x10(-9), OR = 1.42) is likely the susceptibility variant for GD. 20352109

2010
dbSNP: rs231779
rs231779
CTLA4
0.030 GeneticVariation BEFREE Logistic analysis confirmed the contribution of CTLA-4 rs231779 to the development of GD. 19438904

2010