Disease: Myasthenia Gravis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs558702
rs558702
Entrez Id: 717;1589;221527
Gene Symbol: C2;CYP21A2;ZBTB12
C2;CYP21A2;ZBTB12
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