Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3733890
rs3733890
BHMT ; DMGDH
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele 		0.010 GeneticVariation BEFREE A SNP in the homocysteine-related gene, betaine-homocysteine S-methyltransferase (BHMT), rs3733890 (p.R239Q), was significantly associated with omphalocele in both African-Americans and Asians. 22116453

2012