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rs16884711

From SNPedia

Orientationplus
Stabilizedplus
Make rs16884711(A;A)
Make rs16884711(A;C)
Make rs16884711(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position56028975
is asnp
is mentioned by
dbSNPrs16884711
dbSNP (old)rs16884711
ClinGenrs16884711
ebirs16884711
HLIrs16884711
Exacrs16884711
Gnomadrs16884711
Varsomers16884711
Maprs16884711
PheGenIrs16884711
Biobankrs16884711
1000 genomesrs16884711
hgdprs16884711
ensemblrs16884711
gopubmedrs16884711
geneviewrs16884711
scholarrs16884711
googlers16884711
pharmgkbrs16884711
gwascentralrs16884711
openSNPrs16884711
23andMers16884711
23andMe allrs16884711
SNP Nexus

SNPshotrs16884711
SNPdbers16884711
MSV3drs16884711
GWAS Ctlgrs16884711
GMAF0.1602
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 2E-6
Odds Ratio .19 [0.11-0.27] unit increase