rs10224002, PRKAG2

N. diseases: 12
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
0.800 GeneticVariation GWASCAT Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
0.800 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009