Disease: Van der Woude syndrome 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879255245
rs879255245
Entrez Id: 57822
Gene Symbol: GRHL3
GRHL3
CUI: C1847604
Disease:
Van der Woude syndrome 2 		0.800 GeneticVariation UNIPROT Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. 24360809 2014
dbSNP: rs879255245
rs879255245
Entrez Id: 57822
Gene Symbol: GRHL3
GRHL3
CUI: C1847604
Disease:
Van der Woude syndrome 2 		T 0.800 CausalMutation CLINVAR