rs10786691, SUFU

N. diseases: 3
Disease: Congenital cerebral hernia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital cerebral hernia
CUI: C0014065
Disease: Congenital cerebral hernia
0.010 GeneticVariation BEFREE The heterozygous AG allele of rs10786691 was significantly related with NTDs and encephalocele (OR = 1.60, 95% CI: 1.04-2.48, p = 0.034; OR = 2.83, 95% CI: 1.07-7.47, p = 0.036). 24070372 2014