Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909210
rs121909210
Entrez Id: 7045
Gene Symbol: TGFBI
TGFBI
CUI: C1641846
Disease:
Groenouw corneal dystrophy type I (disorder)
0.800 GeneticVariation UNIPROT TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients. 15623763 2005
dbSNP: rs121909210
rs121909210
Entrez Id: 7045
Gene Symbol: TGFBI
TGFBI
CUI: C1641846
Disease:
Groenouw corneal dystrophy type I (disorder)
A 0.800 CausalMutation CLINVAR