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rs11651000

From SNPedia

Orientationplus
Stabilizedplus
Make rs11651000(A;A)
Make rs11651000(A;G)
Make rs11651000(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position47757912
is asnp
is mentioned by
dbSNPrs11651000
dbSNP (classic)rs11651000
ClinGenrs11651000
ebirs11651000
HLIrs11651000
Exacrs11651000
Gnomadrs11651000
Varsomers11651000
LitVarrs11651000
Maprs11651000
PheGenIrs11651000
Biobankrs11651000
1000 genomesrs11651000
hgdprs11651000
ensemblrs11651000
geneviewrs11651000
scholarrs11651000
googlers11651000
pharmgkbrs11651000
gwascentralrs11651000
openSNPrs11651000
23andMers11651000
SNPshotrs11651000
SNPdbers11651000
MSV3drs11651000
GWAS Ctlgrs11651000
GMAF0.1084
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 8E-6
Odds Ratio .19 [0.11-0.27] unit decrease