Have questions? Visit https://www.reddit.com/r/SNPedia

rs12950390

From SNPedia

Orientationplus
Stabilizedplus
Make rs12950390(C;C)
Make rs12950390(C;T)
Make rs12950390(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position47753582
is asnp
is mentioned by
dbSNPrs12950390
dbSNP (classic)rs12950390
ClinGenrs12950390
ebirs12950390
HLIrs12950390
Exacrs12950390
Gnomadrs12950390
Varsomers12950390
LitVarrs12950390
Maprs12950390
PheGenIrs12950390
Biobankrs12950390
1000 genomesrs12950390
hgdprs12950390
ensemblrs12950390
geneviewrs12950390
scholarrs12950390
googlers12950390
pharmgkbrs12950390
gwascentralrs12950390
openSNPrs12950390
23andMers12950390
SNPshotrs12950390
SNPdbers12950390
MSV3drs12950390
GWAS Ctlgrs12950390
GMAF0.2066
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-6
Odds Ratio .17 [0.098-0.239] unit decrease