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rs7661864

From SNPedia

Orientationplus
Stabilizedplus
Make rs7661864(A;A)
Make rs7661864(A;G)
Make rs7661864(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position6734638
is asnp
is mentioned by
dbSNPrs7661864
ebirs7661864
HLIrs7661864
Exacrs7661864
Varsomers7661864
Maprs7661864
PheGenIrs7661864
hapmaprs7661864
1000 genomesrs7661864
hgdprs7661864
ensemblrs7661864
gopubmedrs7661864
geneviewrs7661864
scholarrs7661864
googlers7661864
pharmgkbrs7661864
gwascentralrs7661864
openSNPrs7661864
23andMers7661864
23andMe allrs7661864
SNP Nexus

SNPshotrs7661864
SNPdbers7661864
MSV3drs7661864
GWAS Ctlgrs7661864
GMAF0.3361
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 .33 [0.19-0.47] unit increase