rs2538958
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2538958(A;A) |
Make rs2538958(A;G) |
Make rs2538958(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 147918548 |
Gene | CNTNAP2 |
is a | snp |
is | mentioned by |
dbSNP | rs2538958 |
dbSNP (classic) | rs2538958 |
ClinGen | rs2538958 |
ebi | rs2538958 |
HLI | rs2538958 |
Exac | rs2538958 |
Gnomad | rs2538958 |
Varsome | rs2538958 |
LitVar | rs2538958 |
Map | rs2538958 |
PheGenI | rs2538958 |
Biobank | rs2538958 |
1000 genomes | rs2538958 |
hgdp | rs2538958 |
ensembl | rs2538958 |
geneview | rs2538958 |
scholar | rs2538958 |
rs2538958 | |
pharmgkb | rs2538958 |
gwascentral | rs2538958 |
openSNP | rs2538958 |
23andMe | rs2538958 |
SNPshot | rs2538958 |
SNPdbe | rs2538958 |
MSV3d | rs2538958 |
GWAS Ctlg | rs2538958 |
GMAF | 0.2704 |
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 | 8E-6 |
Odds Ratio | .14 [0.078-0.2] unit increase |