rs17342717
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
Make rs17342717(C;T) |
Make rs17342717(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 25821542 |
Gene | SLC17A1 |
is a | snp |
is | mentioned by |
dbSNP | rs17342717 |
dbSNP (classic) | rs17342717 |
ClinGen | rs17342717 |
ebi | rs17342717 |
HLI | rs17342717 |
Exac | rs17342717 |
Gnomad | rs17342717 |
Varsome | rs17342717 |
LitVar | rs17342717 |
Map | rs17342717 |
PheGenI | rs17342717 |
Biobank | rs17342717 |
1000 genomes | rs17342717 |
hgdp | rs17342717 |
ensembl | rs17342717 |
geneview | rs17342717 |
scholar | rs17342717 |
rs17342717 | |
pharmgkb | rs17342717 |
gwascentral | rs17342717 |
openSNP | rs17342717 |
23andMe | rs17342717 |
SNPshot | rs17342717 |
SNPdbe | rs17342717 |
MSV3d | rs17342717 |
GWAS Ctlg | rs17342717 |
GMAF | 0.03765 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20927387![]() |
Trait | |
Title | A genome-wide association study of red blood cell traits using the electronic medical record |
Risk Allele | T |
P-val | 5E-8 |
Odds Ratio | 0.38 [0.24-0.52] unit increase |
GWAS snp | |
---|---|
PMID | [PMID 21208937![]() |
Trait | |
Title | Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels |
Risk Allele | C |
P-val | 5E-9 |
Odds Ratio | 36.5000 [24.27-48.73] ng/ml decrease |
GWAS snp | |
---|---|
PMID | [PMID 21149283![]() |
Trait | |
Title | Novel Association to the Proprotein Convertase PCSK7 Gene Locus Revealed by Analysing Soluble Transferrin Receptor (sTfR) Levels |
Risk Allele | T |
P-val | 9E-10 |
Odds Ratio | 0.0870 [0.06-0.12] unit increase |