Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs767689418
rs767689418
Entrez Id: 23370
Gene Symbol: ARHGEF18
ARHGEF18
CUI: C4479481
Disease:
RETINITIS PIGMENTOSA 78
T 0.700 CausalMutation CLINVAR