Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs73212431
rs73212431
Entrez Id: 7555
Gene Symbol: CNBP
CNBP
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1871922
rs1871922
Entrez Id: 7555;105374101
Gene Symbol: CNBP;LOC105374101
CNBP;LOC105374101
CUI: C2931689
Disease:
Dystrophia myotonica 2 		0.010 GeneticVariation BEFREE In addition, the single-nucleotide polymorphism (SNP) rs1871922 located in the first intron of DM2 was genotyped. 21224892 2011