rs1604897
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1604897(C;C) |
Make rs1604897(C;T) |
Make rs1604897(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 121170070 |
is a | snp |
is | mentioned by |
dbSNP | rs1604897 |
dbSNP (classic) | rs1604897 |
ClinGen | rs1604897 |
ebi | rs1604897 |
HLI | rs1604897 |
Exac | rs1604897 |
Gnomad | rs1604897 |
Varsome | rs1604897 |
LitVar | rs1604897 |
Map | rs1604897 |
PheGenI | rs1604897 |
Biobank | rs1604897 |
1000 genomes | rs1604897 |
hgdp | rs1604897 |
ensembl | rs1604897 |
geneview | rs1604897 |
scholar | rs1604897 |
rs1604897 | |
pharmgkb | rs1604897 |
gwascentral | rs1604897 |
openSNP | rs1604897 |
23andMe | rs1604897 |
SNPshot | rs1604897 |
SNPdbe | rs1604897 |
MSV3d | rs1604897 |
GWAS Ctlg | rs1604897 |
GMAF | 0.3338 |
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 | .19 [0.1-0.27] unit decrease |