rs1476413, MTHFR

N. diseases: 10
Disease: Meningomyelocele ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
0.010 GeneticVariation BEFREE In addition, we observed five SNPs (rs13306561, rs2274976, rs2066462, rs12121543, and rs1476413) in the MTHFR gene not previously shown to associate with MM. 22241680 2012