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rs6969802

From SNPedia

Orientationplus
Stabilizedplus
Make rs6969802(A;A)
Make rs6969802(A;G)
Make rs6969802(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position113009359
is asnp
is mentioned by
dbSNPrs6969802
ebirs6969802
HLIrs6969802
Exacrs6969802
Varsomers6969802
Maprs6969802
PheGenIrs6969802
hapmaprs6969802
1000 genomesrs6969802
hgdprs6969802
ensemblrs6969802
gopubmedrs6969802
geneviewrs6969802
scholarrs6969802
googlers6969802
pharmgkbrs6969802
gwascentralrs6969802
openSNPrs6969802
23andMers6969802
23andMe allrs6969802
SNP Nexus

SNPshotrs6969802
SNPdbers6969802
MSV3drs6969802
GWAS Ctlgrs6969802
GMAF0.1171
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 5E-6
Odds Ratio .26 [0.15-0.37] unit decrease