rs5764106
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5764106(C;C) |
Make rs5764106(C;T) |
Make rs5764106(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 44165407 |
Gene | PARVB |
is a | snp |
is | mentioned by |
dbSNP | rs5764106 |
dbSNP (classic) | rs5764106 |
ClinGen | rs5764106 |
ebi | rs5764106 |
HLI | rs5764106 |
Exac | rs5764106 |
Gnomad | rs5764106 |
Varsome | rs5764106 |
LitVar | rs5764106 |
Map | rs5764106 |
PheGenI | rs5764106 |
Biobank | rs5764106 |
1000 genomes | rs5764106 |
hgdp | rs5764106 |
ensembl | rs5764106 |
geneview | rs5764106 |
scholar | rs5764106 |
rs5764106 | |
pharmgkb | rs5764106 |
gwascentral | rs5764106 |
openSNP | rs5764106 |
23andMe | rs5764106 |
SNPshot | rs5764106 |
SNPdbe | rs5764106 |
MSV3d | rs5764106 |
GWAS Ctlg | rs5764106 |
GMAF | 0.4348 |
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 | 5E-6 |
Odds Ratio | .19 [0.11-0.27] unit decrease |