TXN2, thioredoxin 2, 25828

N. diseases: 76; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038219
Disease: Status Dysraphicus
Status Dysraphicus
0.300 Biomarker disease CTD_human Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida. 19165900 2009