Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2372851
rs2372851
Entrez Id: 7123;23016
Gene Symbol: CLEC3B;EXOSC7
CLEC3B;EXOSC7
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs13963
rs13963
Entrez Id: 7123;23016
Gene Symbol: CLEC3B;EXOSC7
CLEC3B;EXOSC7
CUI: C0027765
Disease:
nervous system disorder 		0.010 GeneticVariation BEFREE Although our findings do not support an association between CLEC3B p.S106G and aging without neurological disease (P=0.89), we confirmed the association between the APOE ε2 allele and better survival without neurological disease (P=0.001). 31570938 2019