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rs4869266

From SNPedia

Orientationplus
Stabilizedplus
Make rs4869266(A;A)
Make rs4869266(A;G)
Make rs4869266(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position96151236
GeneCTD-2337A12.1
is asnp
is mentioned by
dbSNPrs4869266
ebirs4869266
HLIrs4869266
Exacrs4869266
Varsomers4869266
Maprs4869266
PheGenIrs4869266
hapmaprs4869266
1000 genomesrs4869266
hgdprs4869266
ensemblrs4869266
gopubmedrs4869266
geneviewrs4869266
scholarrs4869266
googlers4869266
pharmgkbrs4869266
gwascentralrs4869266
openSNPrs4869266
23andMers4869266
23andMe allrs4869266
SNP Nexus

SNPshotrs4869266
SNPdbers4869266
MSV3drs4869266
GWAS Ctlgrs4869266
GMAF0.3783
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 3E-6
Odds Ratio .15 [0.088-0.216] unit increase