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rs1039443

From SNPedia

Orientationplus
Stabilizedplus
Make rs1039443(C;C)
Make rs1039443(C;T)
Make rs1039443(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position16037993
is asnp
is mentioned by
dbSNPrs1039443
dbSNP (classic)rs1039443
ClinGenrs1039443
ebirs1039443
HLIrs1039443
Exacrs1039443
Gnomadrs1039443
Varsomers1039443
LitVarrs1039443
Maprs1039443
PheGenIrs1039443
Biobankrs1039443
1000 genomesrs1039443
hgdprs1039443
ensemblrs1039443
geneviewrs1039443
scholarrs1039443
googlers1039443
pharmgkbrs1039443
gwascentralrs1039443
openSNPrs1039443
23andMers1039443
SNPshotrs1039443
SNPdbers1039443
MSV3drs1039443
GWAS Ctlgrs1039443
GMAF0.1676
Max Magnitude0
? (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 .22 [0.12-0.32] unit decrease