Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918218
rs121918218
Entrez Id: 81839
Gene Symbol: VANGL1
VANGL1
CUI: C1838568
Disease:
Sacral defect and anterior sacral meningocele
0.700 GeneticVariation UNIPROT Mutations in VANGL1 associated with neural-tube defects. 17409324 2007