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rs4821897

From SNPedia

Orientationplus
Stabilizedplus
Make rs4821897(A;A)
Make rs4821897(A;G)
Make rs4821897(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position39439582
is asnp
is mentioned by
dbSNPrs4821897
ebirs4821897
HLIrs4821897
Exacrs4821897
Varsomers4821897
Maprs4821897
PheGenIrs4821897
hapmaprs4821897
1000 genomesrs4821897
hgdprs4821897
ensemblrs4821897
gopubmedrs4821897
geneviewrs4821897
scholarrs4821897
googlers4821897
pharmgkbrs4821897
gwascentralrs4821897
openSNPrs4821897
23andMers4821897
23andMe allrs4821897
SNP Nexus

SNPshotrs4821897
SNPdbers4821897
MSV3drs4821897
GWAS Ctlgrs4821897
GMAF0.1841
Max Magnitude
? (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 G
P-val 4E-18
Odds Ratio .30 [0.23-0.36] unit decrease