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rs10131728

From SNPedia

Orientationplus
Stabilizedplus
Make rs10131728(C;C)
Make rs10131728(C;T)
Make rs10131728(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81168979
is asnp
is mentioned by
dbSNPrs10131728
ebirs10131728
HLIrs10131728
Exacrs10131728
Varsomers10131728
Maprs10131728
PheGenIrs10131728
hapmaprs10131728
1000 genomesrs10131728
hgdprs10131728
ensemblrs10131728
gopubmedrs10131728
geneviewrs10131728
scholarrs10131728
googlers10131728
pharmgkbrs10131728
gwascentralrs10131728
openSNPrs10131728
23andMers10131728
23andMe allrs10131728
SNP Nexus

SNPshotrs10131728
SNPdbers10131728
MSV3drs10131728
GWAS Ctlgrs10131728
GMAF0.0854
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 2E-7
Odds Ratio .24 [0.15-0.33] unit increase