Disease: RETINITIS PIGMENTOSA 37 (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567160967
rs1567160967
Entrez Id: 10002
Gene Symbol: NR2E3
NR2E3
CUI: C1970163
Disease:
RETINITIS PIGMENTOSA 37 (disorder) 		T 0.700 CausalMutation CLINVAR