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rs10764775

From SNPedia

Orientationplus
Stabilizedplus
Make rs10764775(C;C)
Make rs10764775(C;T)
Make rs10764775(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position128435544
is asnp
is mentioned by
dbSNPrs10764775
ebirs10764775
HLIrs10764775
Exacrs10764775
Varsomers10764775
Maprs10764775
PheGenIrs10764775
hapmaprs10764775
1000 genomesrs10764775
hgdprs10764775
ensemblrs10764775
gopubmedrs10764775
geneviewrs10764775
scholarrs10764775
googlers10764775
pharmgkbrs10764775
gwascentralrs10764775
openSNPrs10764775
23andMers10764775
23andMe allrs10764775
SNP Nexus

SNPshotrs10764775
SNPdbers10764775
MSV3drs10764775
GWAS Ctlgrs10764775
GMAF0.4853
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 6E-6
Odds Ratio .14 [0.081-0.206] unit increase