Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2187668
rs2187668
Entrez Id: 3117;3118;107986589
Gene Symbol: HLA-DQA1;HLA-DQA2;LOC107986589
HLA-DQA1;HLA-DQA2;LOC107986589
CUI: C0026896
Disease:
Myasthenia Gravis
0.700 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271 2012