Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs606231285
rs606231285
Entrez Id: 11340;29880
Gene Symbol: EXOSC8;ALG5
EXOSC8;ALG5
CUI: C4015160
Disease:
PONTOCEREBELLAR HYPOPLASIA, TYPE 1C 		T 0.800 CausalMutation CLINVAR
dbSNP: rs606231285
rs606231285
Entrez Id: 11340;29880
Gene Symbol: EXOSC8;ALG5
EXOSC8;ALG5
CUI: C4015160
Disease:
PONTOCEREBELLAR HYPOPLASIA, TYPE 1C 		0.800 GeneticVariation UNIPROT
dbSNP: rs17054796
rs17054796
Entrez Id: 29880
Gene Symbol: ALG5
ALG5
CUI: C2697758
Disease:
Interleukin 10 Measurement 		C 0.700 GeneticVariation GWASCAT Genome-wide associated loci influencing interleukin (IL)-10, IL-1Ra, and IL-6 levels in African Americans. 22205395 2012