TFR2, transferrin receptor 2, 7036

N. diseases: 92; N. variants: 50
Disease: Hematocrit procedure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7385804
rs7385804
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0018935
Disease:
Hematocrit procedure 		C 0.800 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
dbSNP: rs7385804
rs7385804
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0018935
Disease:
Hematocrit procedure 		C 0.800 GeneticVariation GWASCAT Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009