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rs11678036

From SNPedia

Orientationplus
Stabilizedplus
Make rs11678036(C;C)
Make rs11678036(C;T)
Make rs11678036(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position185160008
is asnp
is mentioned by
dbSNPrs11678036
ebirs11678036
HLIrs11678036
Exacrs11678036
Varsomers11678036
Maprs11678036
PheGenIrs11678036
hapmaprs11678036
1000 genomesrs11678036
hgdprs11678036
ensemblrs11678036
gopubmedrs11678036
geneviewrs11678036
scholarrs11678036
googlers11678036
pharmgkbrs11678036
gwascentralrs11678036
openSNPrs11678036
23andMers11678036
23andMe allrs11678036
SNP Nexus

SNPshotrs11678036
SNPdbers11678036
MSV3drs11678036
GWAS Ctlgrs11678036
GMAF0.4564
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 6E-6
Odds Ratio .15 [0.082-0.209] unit increase