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rs11079764

From SNPedia

Orientationplus
Stabilizedplus
Make rs11079764(A;A)
Make rs11079764(A;G)
Make rs11079764(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position47232327
is asnp
is mentioned by
dbSNPrs11079764
dbSNP (classic)rs11079764
ClinGenrs11079764
ebirs11079764
HLIrs11079764
Exacrs11079764
Gnomadrs11079764
Varsomers11079764
LitVarrs11079764
Maprs11079764
PheGenIrs11079764
Biobankrs11079764
1000 genomesrs11079764
hgdprs11079764
ensemblrs11079764
geneviewrs11079764
scholarrs11079764
googlers11079764
pharmgkbrs11079764
gwascentralrs11079764
openSNPrs11079764
23andMers11079764
SNPshotrs11079764
SNPdbers11079764
MSV3drs11079764
GWAS Ctlgrs11079764
GMAF0.3802
Max Magnitude0
? (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 5E-6
Odds Ratio .18 [0.1-0.26] unit decrease