SFTA2, surfactant associated 2, 389376

N. diseases: 25; N. variants: 13
Disease: Myasthenia Gravis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3132580
rs3132580
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
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