Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7109587
rs7109587
Entrez Id: 4676
Gene Symbol: NAP1L4
NAP1L4
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7948848
rs7948848
Entrez Id: 4676
Gene Symbol: NAP1L4
NAP1L4
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4758622
rs4758622
Entrez Id: 4676
Gene Symbol: NAP1L4
NAP1L4
CUI: C0200695
Disease:
Fetal hemoglobin determination 		0.700 GeneticVariation GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008