SLC17A3, solute carrier family 17 member 3, 10786

N. diseases: 21; N. variants: 64
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: rs17271121
rs17271121
Entrez Id: 10786
Gene Symbol: SLC17A3
SLC17A3
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012