Disease: Corneal dystrophy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554579878
rs1554579878
Entrez Id: 79977;107986961;107986962
Gene Symbol: GRHL2;LOC107986961;LOC107986962
GRHL2;LOC107986961;LOC107986962
CUI: C0010036
Disease:
Corneal dystrophy 		T 0.700 GeneticVariation CLINVAR Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4. 29499165 2018