rs1673866
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1673866(A;A) |
Make rs1673866(A;G) |
Make rs1673866(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 103794592 |
is a | snp |
is | mentioned by |
dbSNP | rs1673866 |
dbSNP (classic) | rs1673866 |
ClinGen | rs1673866 |
ebi | rs1673866 |
HLI | rs1673866 |
Exac | rs1673866 |
Gnomad | rs1673866 |
Varsome | rs1673866 |
LitVar | rs1673866 |
Map | rs1673866 |
PheGenI | rs1673866 |
Biobank | rs1673866 |
1000 genomes | rs1673866 |
hgdp | rs1673866 |
ensembl | rs1673866 |
geneview | rs1673866 |
scholar | rs1673866 |
rs1673866 | |
pharmgkb | rs1673866 |
gwascentral | rs1673866 |
openSNP | rs1673866 |
23andMe | rs1673866 |
SNPshot | rs1673866 |
SNPdbe | rs1673866 |
MSV3d | rs1673866 |
GWAS Ctlg | rs1673866 |
GMAF | 0.2383 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23382691![]() |
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 | 7E-6 |
Odds Ratio | .14 [0.081-0.206] unit increase |