SLC17A3, solute carrier family 17 member 3, 10786

N. diseases: 21; N. variants: 64
Disease: Red Blood Cell Count measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17271121
rs17271121
Entrez Id: 10786
Gene Symbol: SLC17A3
SLC17A3
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
dbSNP: rs3887266
rs3887266
Entrez Id: 10786
Gene Symbol: SLC17A3
SLC17A3
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
dbSNP: rs717551
rs717551
Entrez Id: 10786
Gene Symbol: SLC17A3
SLC17A3
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009