Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs184088518
rs184088518
Entrez Id: 112398;100529264
Gene Symbol: EGLN2;RAB4B-EGLN2
EGLN2;RAB4B-EGLN2
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019