rs397507444, MTHFR

N. diseases: 306
Disease: Cleft Palate ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cleft Palate
CUI: C0008925
Disease: Cleft Palate
0.010 GeneticVariation BEFREE The pooled results revealed no statistical association between infant and maternal C677T and A1298C variants and risk of cleft lip with or without palate (CL/P) or cleft palate only (CPO), except for the maternal 677TT genotype for CL/P, the OR was 1.32 (95% confidence interval [CI], 1.06-1.63) as compared to the normal 677CC genotype. 22450905 2012