SLC17A1, solute carrier family 17 member 1, 6568

N. diseases: 23; N. variants: 164
Disease: Corpuscular Hemoglobin Concentration Mean ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1165178
rs1165178
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012