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rs10115586

From SNPedia

Orientationplus
Stabilizedplus
Make rs10115586(C;C)
Make rs10115586(C;T)
Make rs10115586(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position117796733
is asnp
is mentioned by
dbSNPrs10115586
ebirs10115586
HLIrs10115586
Exacrs10115586
Varsomers10115586
Maprs10115586
PheGenIrs10115586
hapmaprs10115586
1000 genomesrs10115586
hgdprs10115586
ensemblrs10115586
gopubmedrs10115586
geneviewrs10115586
scholarrs10115586
googlers10115586
pharmgkbrs10115586
gwascentralrs10115586
openSNPrs10115586
23andMers10115586
23andMe allrs10115586
SNP Nexus

SNPshotrs10115586
SNPdbers10115586
MSV3drs10115586
GWAS Ctlgrs10115586
GMAF0.247
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 5E-7
Odds Ratio .17 [0.1-0.23] unit decrease