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rs10796849

From SNPedia

Orientationplus
Stabilizedplus
Make rs10796849(C;C)
Make rs10796849(C;G)
Make rs10796849(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position69787644
is asnp
is mentioned by
dbSNPrs10796849
ebirs10796849
HLIrs10796849
Exacrs10796849
Varsomers10796849
Maprs10796849
PheGenIrs10796849
hapmaprs10796849
1000 genomesrs10796849
hgdprs10796849
ensemblrs10796849
gopubmedrs10796849
geneviewrs10796849
scholarrs10796849
googlers10796849
pharmgkbrs10796849
gwascentralrs10796849
openSNPrs10796849
23andMers10796849
23andMe allrs10796849
SNP Nexus

SNPshotrs10796849
SNPdbers10796849
MSV3drs10796849
GWAS Ctlgrs10796849
GMAF0.3907
Max Magnitude
? (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 6E-6
Odds Ratio .61 [0.35-0.88] unit decrease