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rs10466868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs10466868(G;T)
Make rs10466868(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position131455375
is asnp
is mentioned by
dbSNPrs10466868
ebirs10466868
HLIrs10466868
Exacrs10466868
Varsomers10466868
Maprs10466868
PheGenIrs10466868
hapmaprs10466868
1000 genomesrs10466868
hgdprs10466868
ensemblrs10466868
gopubmedrs10466868
geneviewrs10466868
scholarrs10466868
googlers10466868
pharmgkbrs10466868
gwascentralrs10466868
openSNPrs10466868
23andMers10466868
23andMe allrs10466868
SNP Nexus

SNPshotrs10466868
SNPdbers10466868
MSV3drs10466868
GWAS Ctlgrs10466868
GMAF0.05234
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Erythropoietin (EPO) protein levels


GET Evidence
rs10466868
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0859375
summary