Disease: Reasoning ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74412765
rs74412765
Entrez Id: 112399;102724945;105370445
Gene Symbol: EGLN3;LOC102724945;EGLN3-AS1
EGLN3;LOC102724945;EGLN3-AS1
CUI: C0684328
Disease:
Reasoning 		T 0.700 GeneticVariation GWASCAT Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. 29907492 2018