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rs7749924

From SNPedia

Orientationplus
Stabilizedplus
Make rs7749924(C;C)
Make rs7749924(C;T)
Make rs7749924(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position30830214
GeneLINC00243
is asnp
is mentioned by
dbSNPrs7749924
ebirs7749924
HLIrs7749924
Exacrs7749924
Varsomers7749924
Maprs7749924
PheGenIrs7749924
hapmaprs7749924
1000 genomesrs7749924
hgdprs7749924
ensemblrs7749924
gopubmedrs7749924
geneviewrs7749924
scholarrs7749924
googlers7749924
pharmgkbrs7749924
gwascentralrs7749924
openSNPrs7749924
23andMers7749924
23andMe allrs7749924
SNP Nexus

SNPshotrs7749924
SNPdbers7749924
MSV3drs7749924
GWAS Ctlgrs7749924
GMAF0.1345
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 8E-6
Odds Ratio .22 [0.12-0.32] unit increase