SEC14L2, SEC14 like lipid binding 2, 23541

N. diseases: 198; N. variants: 2
Disease: Myasthenia Gravis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.010 GeneticVariation disease BEFREE In conclusion, susceptibility to MG is not primarily conferred by TAP alleles in the extended DR3 haplotype. 9062975 1997