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rs2094962

From SNPedia

Orientationminus
Stabilizedminus
Make rs2094962(A;A)
Make rs2094962(A;G)
Make rs2094962(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position134924613
is asnp
is mentioned by
dbSNPrs2094962
dbSNP (classic)rs2094962
ClinGenrs2094962
ebirs2094962
HLIrs2094962
Exacrs2094962
Gnomadrs2094962
Varsomers2094962
LitVarrs2094962
Maprs2094962
PheGenIrs2094962
Biobankrs2094962
1000 genomesrs2094962
hgdprs2094962
ensemblrs2094962
geneviewrs2094962
scholarrs2094962
googlers2094962
pharmgkbrs2094962
gwascentralrs2094962
openSNPrs2094962
23andMers2094962
SNPshotrs2094962
SNPdbers2094962
MSV3drs2094962
GWAS Ctlgrs2094962
GMAF0.2433
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 C
P-val 5E-6
Odds Ratio .24 [0.14-0.34] unit decrease