rs1122979
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1122979(C;C) |
Make rs1122979(C;T) |
Make rs1122979(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 151217985 |
Gene | ABCF2 |
is a | snp |
is | mentioned by |
dbSNP | rs1122979 |
dbSNP (classic) | rs1122979 |
ClinGen | rs1122979 |
ebi | rs1122979 |
HLI | rs1122979 |
Exac | rs1122979 |
Gnomad | rs1122979 |
Varsome | rs1122979 |
LitVar | rs1122979 |
Map | rs1122979 |
PheGenI | rs1122979 |
Biobank | rs1122979 |
1000 genomes | rs1122979 |
hgdp | rs1122979 |
ensembl | rs1122979 |
geneview | rs1122979 |
scholar | rs1122979 |
rs1122979 | |
pharmgkb | rs1122979 |
gwascentral | rs1122979 |
openSNP | rs1122979 |
23andMe | rs1122979 |
SNPshot | rs1122979 |
SNPdbe | rs1122979 |
MSV3d | rs1122979 |
GWAS Ctlg | rs1122979 |
GMAF | 0.06107 |
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 | G |
P-val | 7E-6 |
Odds Ratio | .22 [0.12-0.32] unit decrease |