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rs17348299

From SNPedia

Orientationplus
Stabilizedplus
Make rs17348299(A;A)
Make rs17348299(A;C)
Make rs17348299(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position56027067
is asnp
is mentioned by
dbSNPrs17348299
ebirs17348299
HLIrs17348299
Exacrs17348299
Varsomers17348299
Maprs17348299
PheGenIrs17348299
hapmaprs17348299
1000 genomesrs17348299
hgdprs17348299
ensemblrs17348299
gopubmedrs17348299
geneviewrs17348299
scholarrs17348299
googlers17348299
pharmgkbrs17348299
gwascentralrs17348299
openSNPrs17348299
23andMers17348299
23andMe allrs17348299
SNP Nexus

SNPshotrs17348299
SNPdbers17348299
MSV3drs17348299
GWAS Ctlgrs17348299
GMAF0.09734
Max Magnitude
? (A;A) (A;C) (C;C) 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 2E-7
Odds Ratio .23 [0.14-0.32] unit increase