Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11338569
rs11338569
Entrez Id: 10541
Gene Symbol: ANP32B
ANP32B
CUI: C0014772
Disease:
Red Blood Cell Count measurement
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11338569
rs11338569
Entrez Id: 10541
Gene Symbol: ANP32B
ANP32B
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs76917914
rs76917914
Entrez Id: 10541
Gene Symbol: ANP32B
ANP32B
CUI: C0206161
Disease:
Reticulocyte count (procedure)
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016