Disease: Hematocrit procedure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs552708909
rs552708909
Entrez Id: 5639;51070
Gene Symbol: PRRG2;NOSIP
PRRG2;NOSIP
CUI: C0018935
Disease:
Hematocrit procedure 		CT 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016