rs3097645
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3097645(C;C) |
Make rs3097645(C;G) |
Make rs3097645(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32985503 |
is a | snp |
is | mentioned by |
dbSNP | rs3097645 |
dbSNP (classic) | rs3097645 |
ClinGen | rs3097645 |
ebi | rs3097645 |
HLI | rs3097645 |
Exac | rs3097645 |
Gnomad | rs3097645 |
Varsome | rs3097645 |
LitVar | rs3097645 |
Map | rs3097645 |
PheGenI | rs3097645 |
Biobank | rs3097645 |
1000 genomes | rs3097645 |
hgdp | rs3097645 |
ensembl | rs3097645 |
geneview | rs3097645 |
scholar | rs3097645 |
rs3097645 | |
pharmgkb | rs3097645 |
gwascentral | rs3097645 |
openSNP | rs3097645 |
23andMe | rs3097645 |
SNPshot | rs3097645 |
SNPdbe | rs3097645 |
MSV3d | rs3097645 |
GWAS Ctlg | rs3097645 |
GMAF | 0.1125 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 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 | 7E-6 |
Odds Ratio | .21 [0.12-0.3] unit increase |