Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606874
rs267606874
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C3150819
Disease:
RETINITIS PIGMENTOSA 56
C 0.700 CausalMutation CLINVAR