TGM2, transglutaminase 2, 7052

N. diseases: 315; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0399526
Disease: Class III malocclusion
Class III malocclusion
0.010 GeneticVariation disease BEFREE Genotyping results showed that the Matrilin-1 polymorphism haplotype TGC (ht4; 158T, 7987G, and 8572C alleles) had a pronounced risk effect for mandibular prognathism compared with controls (OR = 5.16, 95% Cl = 2.03~13.93, P < 0.01). 20739701 2010