rs7179432
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7179432(C;C) |
Make rs7179432(C;T) |
Make rs7179432(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 93021742 |
Gene | CHD2 |
is a | snp |
is | mentioned by |
dbSNP | rs7179432 |
dbSNP (classic) | rs7179432 |
ClinGen | rs7179432 |
ebi | rs7179432 |
HLI | rs7179432 |
Exac | rs7179432 |
Gnomad | rs7179432 |
Varsome | rs7179432 |
LitVar | rs7179432 |
Map | rs7179432 |
PheGenI | rs7179432 |
Biobank | rs7179432 |
1000 genomes | rs7179432 |
hgdp | rs7179432 |
ensembl | rs7179432 |
geneview | rs7179432 |
scholar | rs7179432 |
rs7179432 | |
pharmgkb | rs7179432 |
gwascentral | rs7179432 |
openSNP | rs7179432 |
23andMe | rs7179432 |
SNPshot | rs7179432 |
SNPdbe | rs7179432 |
MSV3d | rs7179432 |
GWAS Ctlg | rs7179432 |
GMAF | 0.4376 |
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 | 4E-6 |
Odds Ratio | .16 [0.09-0.224] unit decrease |