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rs11568995

From SNPedia

Orientationplus
Stabilizedplus
Make rs11568995(A;A)
Make rs11568995(A;G)
Make rs11568995(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position109976429
GeneEGF
is asnp
is mentioned by
dbSNPrs11568995
ebirs11568995
HLIrs11568995
Exacrs11568995
Varsomers11568995
Maprs11568995
PheGenIrs11568995
hapmaprs11568995
1000 genomesrs11568995
hgdprs11568995
ensemblrs11568995
gopubmedrs11568995
geneviewrs11568995
scholarrs11568995
googlers11568995
pharmgkbrs11568995
gwascentralrs11568995
openSNPrs11568995
23andMers11568995
23andMe allrs11568995
SNP Nexus

SNPshotrs11568995
SNPdbers11568995
MSV3drs11568995
GWAS Ctlgrs11568995
GMAF0.01653
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 5E-6
Odds Ratio 1.62 [0.93-2.32] unit decrease