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rs10995439

From SNPedia

Orientationplus
Stabilizedplus
Make rs10995439(A;A)
Make rs10995439(A;G)
Make rs10995439(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position63107152
is asnp
is mentioned by
dbSNPrs10995439
ebirs10995439
HLIrs10995439
Exacrs10995439
Varsomers10995439
Maprs10995439
PheGenIrs10995439
hapmaprs10995439
1000 genomesrs10995439
hgdprs10995439
ensemblrs10995439
gopubmedrs10995439
geneviewrs10995439
scholarrs10995439
googlers10995439
pharmgkbrs10995439
gwascentralrs10995439
openSNPrs10995439
23andMers10995439
23andMe allrs10995439
SNP Nexus

SNPshotrs10995439
SNPdbers10995439
MSV3drs10995439
GWAS Ctlgrs10995439
GMAF0.3338
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 1E-7
Odds Ratio .16 [0.1-0.22] unit increase