FOLH1, folate hydrolase 1, 2346

N. diseases: 311; N. variants: 20
Disease: Congenital cerebral hernia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202676
rs202676
Entrez Id: 2346
Gene Symbol: FOLH1
FOLH1
CUI: C0014065
Disease:
Congenital cerebral hernia 		0.010 GeneticVariation BEFREE Although no significant differences in rs202676 genotype or allele frequencies were found between the NTD and control groups, the combined AG+GG genotype group was significantly associated with anencephaly (p = 0.03, OR = 2.11, 95% CI, 1.11-4.01), but not with spina bifida or encephalocele. 22124883 2012