Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.820 GeneticVariation BEFREE Celiac disease associated SNP rs17810546 is located in a gene silencing region. 31726085

2020
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.820 GeneticVariation BEFREE The available data indicated the minor allele C of rs2816316 was negatively associated with CD (C vs. A: OR = 0.77, 95% CI = 0.74-0.80), and a positive association was found for the minor allele G of rs17810546 (G vs. A: OR = 1.37, 95% CI = 1.31-1.43). 27043536

2016
dbSNP: rs17810546
rs17810546
IL12A-AS1
G 0.820 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010
dbSNP: rs17810546
rs17810546
IL12A-AS1
G 0.820 GeneticVariation GWASDB Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010
dbSNP: rs17810546
rs17810546
IL12A-AS1
G 0.820 GeneticVariation GWASDB Newly identified genetic risk variants for celiac disease related to the immune response. 18311140

2008
dbSNP: rs17810546
rs17810546
IL12A-AS1
G 0.820 GeneticVariation GWASCAT Newly identified genetic risk variants for celiac disease related to the immune response. 18311140

2008