{{Rsnum
|rsid=17342717
|Gene=SLC17A1
|Chromosome=6
|position=25821542
|Orientation=plus
|GMAF=0.03765
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC17A1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 83.2 | 15.9 | 0.9
| HCB | 98.5 | 1.5 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 96.5 | 3.5 | 0.0
| CHB | 98.5 | 1.5 | 0.0
| CHD | 97.2 | 2.8 | 0.0
| GIH | 96.0 | 4.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 94.8 | 5.2 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 89.2 | 10.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20927387
|Trait=None
|Title=A genome-wide association study of red blood cell traits using the electronic medical record
|RiskAllele=T
|Pval=5E-8
|OR=0.38
|ORtxt=[0.24-0.52] unit increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=21208937
|Trait=None
|Title=Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels
|RiskAllele=C
|Pval=5E-9
|OR=36.5000
|ORtxt=[24.27-48.73] ng/ml decrease
|OA=1
}}
{{PMID Auto GWAS
|PMID=21149283
|Trait=None
|Title=Novel Association to the Proprotein Convertase PCSK7 Gene Locus Revealed by Analysing Soluble Transferrin Receptor (sTfR) Levels
|RiskAllele=T
|Pval=9E-10
|OR=0.0870
|ORtxt=[0.06-0.12] unit increase
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}