rs1801394, FASTKD3;MTRR

N. diseases: 101
Disease: Avitaminosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Avitaminosis
CUI: C0376286
Disease: Avitaminosis
0.010 GeneticVariation BEFREE The association of MTRR 66A>G polymorphism with oxidant stress and disease activity provides rationale for screening vitamin deficiencies in these patients. 17925002 2008