Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398032702
rs398032702
Entrez Id: 147339
Gene Symbol: C18orf25
C18orf25
CUI: C0200633
Disease:
Neutrophil count (procedure)
TA 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016