SLC17A1, solute carrier family 17 member 1, 6568

N. diseases: 23; N. variants: 164
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: rs12200962
rs12200962
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009