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rs4466877

From SNPedia

Orientationplus
Stabilizedplus
Make rs4466877(A;A)
Make rs4466877(A;G)
Make rs4466877(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position114516380
is asnp
is mentioned by
dbSNPrs4466877
ebirs4466877
HLIrs4466877
Exacrs4466877
Varsomers4466877
Maprs4466877
PheGenIrs4466877
hapmaprs4466877
1000 genomesrs4466877
hgdprs4466877
ensemblrs4466877
gopubmedrs4466877
geneviewrs4466877
scholarrs4466877
googlers4466877
pharmgkbrs4466877
gwascentralrs4466877
openSNPrs4466877
23andMers4466877
23andMe allrs4466877
SNP Nexus

SNPshotrs4466877
SNPdbers4466877
MSV3drs4466877
GWAS Ctlgrs4466877
GMAF0.1823
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 9E-7
Odds Ratio .24 [0.15-0.34] unit increase