rs1339738
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1339738(C;C) |
Make rs1339738(C;T) |
Make rs1339738(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 239233804 |
is a | snp |
is | mentioned by |
dbSNP | rs1339738 |
dbSNP (classic) | rs1339738 |
ClinGen | rs1339738 |
ebi | rs1339738 |
HLI | rs1339738 |
Exac | rs1339738 |
Gnomad | rs1339738 |
Varsome | rs1339738 |
LitVar | rs1339738 |
Map | rs1339738 |
PheGenI | rs1339738 |
Biobank | rs1339738 |
1000 genomes | rs1339738 |
hgdp | rs1339738 |
ensembl | rs1339738 |
geneview | rs1339738 |
scholar | rs1339738 |
rs1339738 | |
pharmgkb | rs1339738 |
gwascentral | rs1339738 |
openSNP | rs1339738 |
23andMe | rs1339738 |
SNPshot | rs1339738 |
SNPdbe | rs1339738 |
MSV3d | rs1339738 |
GWAS Ctlg | rs1339738 |
GMAF | 0.07622 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | .29 [0.16-0.42] unit increase |