Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs987233144
rs987233144
Entrez Id: 23370
Gene Symbol: ARHGEF18
ARHGEF18
CUI: C4479481
Disease:
RETINITIS PIGMENTOSA 78
0.800 GeneticVariation UNIPROT
dbSNP: rs987233144
rs987233144
Entrez Id: 23370
Gene Symbol: ARHGEF18
ARHGEF18
CUI: C4479481
Disease:
RETINITIS PIGMENTOSA 78
G 0.800 CausalMutation CLINVAR