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rs17594709

From SNPedia

Orientationplus
Stabilizedplus
Make rs17594709(A;A)
Make rs17594709(A;G)
Make rs17594709(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position12179909
is asnp
is mentioned by
dbSNPrs17594709
ebirs17594709
HLIrs17594709
Exacrs17594709
Varsomers17594709
Maprs17594709
PheGenIrs17594709
hapmaprs17594709
1000 genomesrs17594709
hgdprs17594709
ensemblrs17594709
gopubmedrs17594709
geneviewrs17594709
scholarrs17594709
googlers17594709
pharmgkbrs17594709
gwascentralrs17594709
openSNPrs17594709
23andMers17594709
23andMe allrs17594709
SNP Nexus

SNPshotrs17594709
SNPdbers17594709
MSV3drs17594709
GWAS Ctlgrs17594709
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 .16 [0.09-0.225] unit decrease