SLC17A1, solute carrier family 17 member 1, 6568

N. diseases: 23; N. variants: 164
Disease: Finding of Mean Corpuscular Hemoglobin ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17342717
rs17342717
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.800 GeneticVariation GWASDB Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. 22560525 2012
dbSNP: rs17342717
rs17342717
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.800 GeneticVariation GWASCAT A genome-wide association study of red blood cell traits using the electronic medical record. 20927387 2010