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rs17621444

From SNPedia

Orientationplus
Stabilizedplus
Make rs17621444(C;C)
Make rs17621444(C;T)
Make rs17621444(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position120062026
is asnp
is mentioned by
dbSNPrs17621444
ebirs17621444
HLIrs17621444
Exacrs17621444
Varsomers17621444
Maprs17621444
PheGenIrs17621444
hapmaprs17621444
1000 genomesrs17621444
hgdprs17621444
ensemblrs17621444
gopubmedrs17621444
geneviewrs17621444
scholarrs17621444
googlers17621444
pharmgkbrs17621444
gwascentralrs17621444
openSNPrs17621444
23andMers17621444
23andMe allrs17621444
SNP Nexus

SNPshotrs17621444
SNPdbers17621444
MSV3drs17621444
GWAS Ctlgrs17621444
GMAF0.1593
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 3E-6
Odds Ratio .16 [0.095-0.233] unit increase