Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs750740765
rs750740765
Entrez Id: 10002
Gene Symbol: NR2E3
NR2E3
CUI: C4085590
Disease:
Cone-Rod Dystrophies
T 0.700 CausalMutation CLINVAR