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rs11774682

From SNPedia

Orientationplus
Stabilizedplus
Make rs11774682(C;C)
Make rs11774682(C;T)
Make rs11774682(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position31176759
is asnp
is mentioned by
dbSNPrs11774682
ebirs11774682
HLIrs11774682
Exacrs11774682
Varsomers11774682
Maprs11774682
PheGenIrs11774682
hapmaprs11774682
1000 genomesrs11774682
hgdprs11774682
ensemblrs11774682
gopubmedrs11774682
geneviewrs11774682
scholarrs11774682
googlers11774682
pharmgkbrs11774682
gwascentralrs11774682
openSNPrs11774682
23andMers11774682
23andMe allrs11774682
SNP Nexus

SNPshotrs11774682
SNPdbers11774682
MSV3drs11774682
GWAS Ctlgrs11774682
GMAF0.01837
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23382691OA-icon.png]
Trait IgG glycosylation
Title Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
Risk Allele C
P-val 1E-6
Odds Ratio .83 [0.49-1.16] unit decrease