Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607167
rs267607167
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2
CUI: C3891448
Disease:
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
0.800 GeneticVariation UNIPROT VANGL2 mutations in human cranial neural-tube defects. 20558380 2010
dbSNP: rs267607168
rs267607168
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2
CUI: C3891448
Disease:
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
0.800 GeneticVariation UNIPROT VANGL2 mutations in human cranial neural-tube defects. 20558380 2010
dbSNP: rs267607167
rs267607167
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2
CUI: C3891448
Disease:
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
T 0.800 SusceptibilityMutation CLINVAR
dbSNP: rs267607168
rs267607168
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2
CUI: C3891448
Disease:
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
C 0.800 SusceptibilityMutation CLINVAR