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rs1364477

From SNPedia

Orientationminus
Stabilizedminus
Make rs1364477(C;C)
Make rs1364477(C;T)
Make rs1364477(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position185319303
is asnp
is mentioned by
dbSNPrs1364477
ebirs1364477
HLIrs1364477
Exacrs1364477
Varsomers1364477
Maprs1364477
PheGenIrs1364477
hapmaprs1364477
1000 genomesrs1364477
hgdprs1364477
ensemblrs1364477
gopubmedrs1364477
geneviewrs1364477
scholarrs1364477
googlers1364477
pharmgkbrs1364477
gwascentralrs1364477
openSNPrs1364477
23andMers1364477
23andMe allrs1364477
SNP Nexus

SNPshotrs1364477
SNPdbers1364477
MSV3drs1364477
GWAS Ctlgrs1364477
GMAF0.2089
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 G
P-val 6E-6
Odds Ratio .18 [0.1-0.26] unit increase