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rs7953959

From SNPedia

Orientationplus
Stabilizedplus
Make rs7953959(C;C)
Make rs7953959(C;T)
Make rs7953959(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position97134362
is asnp
is mentioned by
dbSNPrs7953959
dbSNP (classic)rs7953959
ClinGenrs7953959
ebirs7953959
HLIrs7953959
Exacrs7953959
Gnomadrs7953959
Varsomers7953959
LitVarrs7953959
Maprs7953959
PheGenIrs7953959
Biobankrs7953959
1000 genomesrs7953959
hgdprs7953959
ensemblrs7953959
geneviewrs7953959
scholarrs7953959
googlers7953959
pharmgkbrs7953959
gwascentralrs7953959
openSNPrs7953959
23andMers7953959
SNPshotrs7953959
SNPdbers7953959
MSV3drs7953959
GWAS Ctlgrs7953959
GMAF0.4931
Max Magnitude0
? (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 .14 [0.078-0.2] unit increase