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rs11665307

From SNPedia

Orientationplus
Stabilizedplus
Make rs11665307(C;C)
Make rs11665307(C;T)
Make rs11665307(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position71698064
is asnp
is mentioned by
dbSNPrs11665307
dbSNP (classic)rs11665307
ClinGenrs11665307
ebirs11665307
HLIrs11665307
Exacrs11665307
Gnomadrs11665307
Varsomers11665307
LitVarrs11665307
Maprs11665307
PheGenIrs11665307
Biobankrs11665307
1000 genomesrs11665307
hgdprs11665307
ensemblrs11665307
geneviewrs11665307
scholarrs11665307
googlers11665307
pharmgkbrs11665307
gwascentralrs11665307
openSNPrs11665307
23andMers11665307
SNPshotrs11665307
SNPdbers11665307
MSV3drs11665307
GWAS Ctlgrs11665307
GMAF0.1051
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 3E-7
Odds Ratio .21 [0.13-0.29] unit decrease