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rs17161553

From SNPedia

Orientationplus
Stabilizedplus
Make rs17161553(C;C)
Make rs17161553(C;T)
Make rs17161553(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position100966102
is asnp
is mentioned by
dbSNPrs17161553
ebirs17161553
HLIrs17161553
Exacrs17161553
Varsomers17161553
Maprs17161553
PheGenIrs17161553
hapmaprs17161553
1000 genomesrs17161553
hgdprs17161553
ensemblrs17161553
gopubmedrs17161553
geneviewrs17161553
scholarrs17161553
googlers17161553
pharmgkbrs17161553
gwascentralrs17161553
openSNPrs17161553
23andMers17161553
23andMe allrs17161553
SNP Nexus

SNPshotrs17161553
SNPdbers17161553
MSV3drs17161553
GWAS Ctlgrs17161553
GMAF0.04362
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 1E-6
Odds Ratio 1.69 [1.01-2.38] unit increase