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rs9834373

From SNPedia

Orientationplus
Stabilizedplus
Make rs9834373(G;G)
Make rs9834373(G;T)
Make rs9834373(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position78449847
is asnp
is mentioned by
dbSNPrs9834373
ebirs9834373
HLIrs9834373
Exacrs9834373
Varsomers9834373
Maprs9834373
PheGenIrs9834373
hapmaprs9834373
1000 genomesrs9834373
hgdprs9834373
ensemblrs9834373
gopubmedrs9834373
geneviewrs9834373
scholarrs9834373
googlers9834373
pharmgkbrs9834373
gwascentralrs9834373
openSNPrs9834373
23andMers9834373
23andMe allrs9834373
SNP Nexus

SNPshotrs9834373
SNPdbers9834373
MSV3drs9834373
GWAS Ctlgrs9834373
GMAF0.298
Max Magnitude
? (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 0.0000039999999999999998
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Glycoprotein 130 (GP130, IL6ST) protein levels


GET Evidence
rs9834373
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary