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rs4866334

From SNPedia

Orientationplus
Stabilizedplus
Make rs4866334(C;C)
Make rs4866334(C;T)
Make rs4866334(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position18483542
is asnp
is mentioned by
dbSNPrs4866334
ebirs4866334
HLIrs4866334
Exacrs4866334
Varsomers4866334
Maprs4866334
PheGenIrs4866334
hapmaprs4866334
1000 genomesrs4866334
hgdprs4866334
ensemblrs4866334
gopubmedrs4866334
geneviewrs4866334
scholarrs4866334
googlers4866334
pharmgkbrs4866334
gwascentralrs4866334
openSNPrs4866334
23andMers4866334
23andMe allrs4866334
SNP Nexus

SNPshotrs4866334
SNPdbers4866334
MSV3drs4866334
GWAS Ctlgrs4866334
GMAF0.08494
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 4E-6
Odds Ratio .25 [0.15-0.36] unit decrease