rs435066
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs435066(A;A) |
Make rs435066(A;G) |
Make rs435066(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 68461830 |
is a | snp |
is | mentioned by |
dbSNP | rs435066 |
dbSNP (classic) | rs435066 |
ClinGen | rs435066 |
ebi | rs435066 |
HLI | rs435066 |
Exac | rs435066 |
Gnomad | rs435066 |
Varsome | rs435066 |
LitVar | rs435066 |
Map | rs435066 |
PheGenI | rs435066 |
Biobank | rs435066 |
1000 genomes | rs435066 |
hgdp | rs435066 |
ensembl | rs435066 |
geneview | rs435066 |
scholar | rs435066 |
rs435066 | |
pharmgkb | rs435066 |
gwascentral | rs435066 |
openSNP | rs435066 |
23andMe | rs435066 |
SNPshot | rs435066 |
SNPdbe | rs435066 |
MSV3d | rs435066 |
GWAS Ctlg | rs435066 |
GMAF | 0.3163 |
Max Magnitude | 0 |
? | (A;A) (A;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 | 8E-6 |
Odds Ratio | .18 [0.099-0.254] unit increase |