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rs9636252

From SNPedia

Orientationplus
Stabilizedplus
Make rs9636252(C;C)
Make rs9636252(C;T)
Make rs9636252(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position9119469
is asnp
is mentioned by
dbSNPrs9636252
ebirs9636252
HLIrs9636252
Exacrs9636252
Varsomers9636252
Maprs9636252
PheGenIrs9636252
hapmaprs9636252
1000 genomesrs9636252
hgdprs9636252
ensemblrs9636252
gopubmedrs9636252
geneviewrs9636252
scholarrs9636252
googlers9636252
pharmgkbrs9636252
gwascentralrs9636252
openSNPrs9636252
23andMers9636252
23andMe allrs9636252
SNP Nexus

SNPshotrs9636252
SNPdbers9636252
MSV3drs9636252
GWAS Ctlgrs9636252
GMAF0.4068
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 3E-6
Odds Ratio .15 [0.087-0.215] unit increase