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rs2126200

From SNPedia

Orientationplus
Stabilizedplus
Make rs2126200(C;C)
Make rs2126200(C;G)
Make rs2126200(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position123002368
is asnp
is mentioned by
dbSNPrs2126200
dbSNP (classic)rs2126200
ClinGenrs2126200
ebirs2126200
HLIrs2126200
Exacrs2126200
Gnomadrs2126200
Varsomers2126200
LitVarrs2126200
Maprs2126200
PheGenIrs2126200
Biobankrs2126200
1000 genomesrs2126200
hgdprs2126200
ensemblrs2126200
geneviewrs2126200
scholarrs2126200
googlers2126200
pharmgkbrs2126200
gwascentralrs2126200
openSNPrs2126200
23andMers2126200
SNPshotrs2126200
SNPdbers2126200
MSV3drs2126200
GWAS Ctlgrs2126200
GMAF0.4867
Max Magnitude0
? (C;C) (C;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 C
P-val 7E-6
Odds Ratio .14 [0.078-0.2] unit decrease