Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10224002
rs10224002
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE
G 0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009