rs267607167, VANGL2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
CUI: C3891448
Disease: NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
0.800 GeneticVariation UNIPROT VANGL2 mutations in human cranial neural-tube defects. 20558380 2010
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
CUI: C3891448
Disease: NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
0.800 SusceptibilityMutation CLINVAR