Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4919594
rs4919594
Entrez Id: 340665
Gene Symbol: CYP26C1
CYP26C1
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11187265
rs11187265
Entrez Id: 340665
Gene Symbol: CYP26C1
CYP26C1
CUI: C0038013
Disease:
Ankylosing spondylitis 		0.010 GeneticVariation BEFREE Genetic analysis showed that an exonic CYP26C1 SNP (rs11187265) is not associated with AS. 18050373 2007