Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607167
rs267607167
VANGL2
0.800 GeneticVariation UNIPROT VANGL2 mutations in human cranial neural-tube defects. 20558380

2010
dbSNP: rs267607167
rs267607167
VANGL2
T 0.800 SusceptibilityMutation CLINVAR