rs7953959
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7953959(C;C) |
Make rs7953959(C;T) |
Make rs7953959(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 97134362 |
is a | snp |
is | mentioned by |
dbSNP | rs7953959 |
dbSNP (classic) | rs7953959 |
ClinGen | rs7953959 |
ebi | rs7953959 |
HLI | rs7953959 |
Exac | rs7953959 |
Gnomad | rs7953959 |
Varsome | rs7953959 |
LitVar | rs7953959 |
Map | rs7953959 |
PheGenI | rs7953959 |
Biobank | rs7953959 |
1000 genomes | rs7953959 |
hgdp | rs7953959 |
ensembl | rs7953959 |
geneview | rs7953959 |
scholar | rs7953959 |
rs7953959 | |
pharmgkb | rs7953959 |
gwascentral | rs7953959 |
openSNP | rs7953959 |
23andMe | rs7953959 |
SNPshot | rs7953959 |
SNPdbe | rs7953959 |
MSV3d | rs7953959 |
GWAS Ctlg | rs7953959 |
GMAF | 0.4931 |
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 | 8E-6 |
Odds Ratio | .14 [0.078-0.2] unit increase |