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rs17342717

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs17342717(C;T)
Make rs17342717(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position25821542
GeneSLC17A1
is asnp
is mentioned by
dbSNPrs17342717
dbSNP (classic)rs17342717
ClinGenrs17342717
ebirs17342717
HLIrs17342717
Exacrs17342717
Gnomadrs17342717
Varsomers17342717
LitVarrs17342717
Maprs17342717
PheGenIrs17342717
Biobankrs17342717
1000 genomesrs17342717
hgdprs17342717
ensemblrs17342717
geneviewrs17342717
scholarrs17342717
googlers17342717
pharmgkbrs17342717
gwascentralrs17342717
openSNPrs17342717
23andMers17342717
SNPshotrs17342717
SNPdbers17342717
MSV3drs17342717
GWAS Ctlgrs17342717
GMAF0.03765
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20927387OA-icon.png]
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 21208937OA-icon.png]
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 21149283OA-icon.png]
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