Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554579819
rs1554579819
GRHL2 ; LOC107986961 ; LOC107986962
G 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