rs10764775
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10764775(C;C) |
Make rs10764775(C;T) |
Make rs10764775(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 128435544 |
is a | snp |
is | mentioned by |
dbSNP | rs10764775 |
dbSNP (classic) | rs10764775 |
ClinGen | rs10764775 |
ebi | rs10764775 |
HLI | rs10764775 |
Exac | rs10764775 |
Gnomad | rs10764775 |
Varsome | rs10764775 |
LitVar | rs10764775 |
Map | rs10764775 |
PheGenI | rs10764775 |
Biobank | rs10764775 |
1000 genomes | rs10764775 |
hgdp | rs10764775 |
ensembl | rs10764775 |
geneview | rs10764775 |
scholar | rs10764775 |
rs10764775 | |
pharmgkb | rs10764775 |
gwascentral | rs10764775 |
openSNP | rs10764775 |
23andMe | rs10764775 |
SNPshot | rs10764775 |
SNPdbe | rs10764775 |
MSV3d | rs10764775 |
GWAS Ctlg | rs10764775 |
GMAF | 0.4853 |
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 | 6E-6 |
Odds Ratio | .14 [0.081-0.206] unit increase |