OVOL2, ovo like zinc finger 2, 58495

N. diseases: 58; N. variants: 9
Disease: CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869320627
rs869320627
Entrez Id: 58495
Gene Symbol: OVOL2
OVOL2
CUI: C1852555
Disease:
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT 		ACCGGTTCCGGCGGCCGGGGCTG 0.700 CausalMutation CLINVAR
dbSNP: rs869320628
rs869320628
Entrez Id: 58495
Gene Symbol: OVOL2
OVOL2
CUI: C1852555
Disease:
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT 		G 0.700 CausalMutation CLINVAR
dbSNP: rs869320629
rs869320629
Entrez Id: 58495
Gene Symbol: OVOL2
OVOL2
CUI: C1852555
Disease:
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT 		G 0.700 CausalMutation CLINVAR
dbSNP: rs869320630
rs869320630
Entrez Id: 58495
Gene Symbol: OVOL2
OVOL2
CUI: C1852555
Disease:
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT 		C 0.700 CausalMutation CLINVAR