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rs137699

From SNPedia

Orientationplus
Stabilizedplus
Make rs137699(A;A)
Make rs137699(A;G)
Make rs137699(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position39352849
GeneSYNGR1
is asnp
is mentioned by
dbSNPrs137699
ebirs137699
HLIrs137699
Exacrs137699
Varsomers137699
Maprs137699
PheGenIrs137699
hapmaprs137699
1000 genomesrs137699
hgdprs137699
ensemblrs137699
gopubmedrs137699
geneviewrs137699
scholarrs137699
googlers137699
pharmgkbrs137699
gwascentralrs137699
openSNPrs137699
23andMers137699
23andMe allrs137699
SNP Nexus

SNPshotrs137699
SNPdbers137699
MSV3drs137699
GWAS Ctlgrs137699
GMAF0.3701
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 8E-6
Odds Ratio .16 [0.088-0.225] unit decrease