SLC17A1, solute carrier family 17 member 1, 6568

N. diseases: 23; N. variants: 164
Disease: Ferritin measurement ×
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: C0373607
Disease:
Ferritin measurement 		C 0.700 GeneticVariation GWASCAT Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. 21208937 2011
dbSNP: rs17342717
rs17342717
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C0373607
Disease:
Ferritin measurement 		T 0.700 GeneticVariation GWASCAT Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. 21149283 2011