rs1001579
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1001579(C;C) |
Make rs1001579(C;T) |
Make rs1001579(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 108396257 |
is a | snp |
is | mentioned by |
dbSNP | rs1001579 |
dbSNP (classic) | rs1001579 |
ClinGen | rs1001579 |
ebi | rs1001579 |
HLI | rs1001579 |
Exac | rs1001579 |
Gnomad | rs1001579 |
Varsome | rs1001579 |
LitVar | rs1001579 |
Map | rs1001579 |
PheGenI | rs1001579 |
Biobank | rs1001579 |
1000 genomes | rs1001579 |
hgdp | rs1001579 |
ensembl | rs1001579 |
geneview | rs1001579 |
scholar | rs1001579 |
rs1001579 | |
pharmgkb | rs1001579 |
gwascentral | rs1001579 |
openSNP | rs1001579 |
23andMe | rs1001579 |
SNPshot | rs1001579 |
SNPdbe | rs1001579 |
MSV3d | rs1001579 |
GWAS Ctlg | rs1001579 |
GMAF | 0.1074 |
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 | .18 [0.1-0.26] unit increase |