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rs1673866

From SNPedia

Orientationminus
Stabilizedminus
Make rs1673866(A;A)
Make rs1673866(A;G)
Make rs1673866(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position103794592
is asnp
is mentioned by
dbSNPrs1673866
dbSNP (classic)rs1673866
ClinGenrs1673866
ebirs1673866
HLIrs1673866
Exacrs1673866
Gnomadrs1673866
Varsomers1673866
LitVarrs1673866
Maprs1673866
PheGenIrs1673866
Biobankrs1673866
1000 genomesrs1673866
hgdprs1673866
ensemblrs1673866
geneviewrs1673866
scholarrs1673866
googlers1673866
pharmgkbrs1673866
gwascentralrs1673866
openSNPrs1673866
23andMers1673866
SNPshotrs1673866
SNPdbers1673866
MSV3drs1673866
GWAS Ctlgrs1673866
GMAF0.2383
Max Magnitude0
? (A;A) (A;G) (G;G) 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 7E-6
Odds Ratio .14 [0.081-0.206] unit increase