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rs17124610

From SNPedia

Orientationplus
Stabilizedplus
Make rs17124610(C;C)
Make rs17124610(C;T)
Make rs17124610(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position61155300
is asnp
is mentioned by
dbSNPrs17124610
ebirs17124610
HLIrs17124610
Exacrs17124610
Varsomers17124610
Maprs17124610
PheGenIrs17124610
hapmaprs17124610
1000 genomesrs17124610
hgdprs17124610
ensemblrs17124610
gopubmedrs17124610
geneviewrs17124610
scholarrs17124610
googlers17124610
pharmgkbrs17124610
gwascentralrs17124610
openSNPrs17124610
23andMers17124610
23andMe allrs17124610
SNP Nexus

SNPshotrs17124610
SNPdbers17124610
MSV3drs17124610
GWAS Ctlgrs17124610
GMAF0.06566
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 8E-6
Odds Ratio .67 [0.38-0.97] unit decrease