Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs184088518
rs184088518
EGLN2 ; RAB4B-EGLN2
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs61750953
rs61750953
EGLN2 ; RAB4B-EGLN2
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016