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rs10203166

From SNPedia

Orientationplus
Stabilizedplus
Make rs10203166(C;C)
Make rs10203166(C;T)
Make rs10203166(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position59562570
is asnp
is mentioned by
dbSNPrs10203166
ebirs10203166
HLIrs10203166
Exacrs10203166
Varsomers10203166
Maprs10203166
PheGenIrs10203166
hapmaprs10203166
1000 genomesrs10203166
hgdprs10203166
ensemblrs10203166
gopubmedrs10203166
geneviewrs10203166
scholarrs10203166
googlers10203166
pharmgkbrs10203166
gwascentralrs10203166
openSNPrs10203166
23andMers10203166
23andMe allrs10203166
SNP Nexus

SNPshotrs10203166
SNPdbers10203166
MSV3drs10203166
GWAS Ctlgrs10203166
GMAF0.045
Max Magnitude
? (C;C) (C;T) (T;T) 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 4E-6
Odds Ratio .80 [0.46-1.14] unit increase