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

rs7902627

From SNPedia

Orientationplus
Stabilizedplus
Make rs7902627(A;A)
Make rs7902627(A;C)
Make rs7902627(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position33116159
GeneLOC101929447
is asnp
is mentioned by
dbSNPrs7902627
ebirs7902627
HLIrs7902627
Exacrs7902627
Varsomers7902627
Maprs7902627
PheGenIrs7902627
hapmaprs7902627
1000 genomesrs7902627
hgdprs7902627
ensemblrs7902627
gopubmedrs7902627
geneviewrs7902627
scholarrs7902627
googlers7902627
pharmgkbrs7902627
gwascentralrs7902627
openSNPrs7902627
23andMers7902627
23andMe allrs7902627
SNP Nexus

SNPshotrs7902627
SNPdbers7902627
MSV3drs7902627
GWAS Ctlgrs7902627
GMAF0.2052
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 8E-6
Odds Ratio .20 [0.11-0.29] unit decrease