rs722599
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs722599(C;C) |
Make rs722599(C;T) |
Make rs722599(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 74860740 |
Gene | PROX2 |
is a | snp |
is | mentioned by |
dbSNP | rs722599 |
dbSNP (classic) | rs722599 |
ClinGen | rs722599 |
ebi | rs722599 |
HLI | rs722599 |
Exac | rs722599 |
Gnomad | rs722599 |
Varsome | rs722599 |
LitVar | rs722599 |
Map | rs722599 |
PheGenI | rs722599 |
Biobank | rs722599 |
1000 genomes | rs722599 |
hgdp | rs722599 |
ensembl | rs722599 |
geneview | rs722599 |
scholar | rs722599 |
rs722599 | |
pharmgkb | rs722599 |
gwascentral | rs722599 |
openSNP | rs722599 |
23andMe | rs722599 |
SNPshot | rs722599 |
SNPdbe | rs722599 |
MSV3d | rs722599 |
GWAS Ctlg | rs722599 |
GMAF | 0.3985 |
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 [0.078-0.201] unit increase |