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rs10751776

From SNPedia

Orientationplus
Stabilizedplus
Make rs10751776(A;A)
Make rs10751776(A;C)
Make rs10751776(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position24970252
is asnp
is mentioned by
dbSNPrs10751776
ebirs10751776
HLIrs10751776
Exacrs10751776
Varsomers10751776
Maprs10751776
PheGenIrs10751776
hapmaprs10751776
1000 genomesrs10751776
hgdprs10751776
ensemblrs10751776
gopubmedrs10751776
geneviewrs10751776
scholarrs10751776
googlers10751776
pharmgkbrs10751776
gwascentralrs10751776
openSNPrs10751776
23andMers10751776
23andMe allrs10751776
SNP Nexus

SNPshotrs10751776
SNPdbers10751776
MSV3drs10751776
GWAS Ctlgrs10751776
GMAF0.3379
Max Magnitude
? (A;A) (A;C) (C;C) 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 7E-6
Odds Ratio .15 [0.084-0.213] unit increase