Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766096417
rs766096417
Entrez Id: 10002
Gene Symbol: NR2E3
NR2E3
CUI: C0035334
Disease:
Retinitis Pigmentosa
A 0.700 GeneticVariation CLINVAR