rs7902627
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7902627(A;A) |
Make rs7902627(A;C) |
Make rs7902627(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 33116159 |
Gene | LOC101929447 |
is a | snp |
is | mentioned by |
dbSNP | rs7902627 |
dbSNP (classic) | rs7902627 |
ClinGen | rs7902627 |
ebi | rs7902627 |
HLI | rs7902627 |
Exac | rs7902627 |
Gnomad | rs7902627 |
Varsome | rs7902627 |
LitVar | rs7902627 |
Map | rs7902627 |
PheGenI | rs7902627 |
Biobank | rs7902627 |
1000 genomes | rs7902627 |
hgdp | rs7902627 |
ensembl | rs7902627 |
geneview | rs7902627 |
scholar | rs7902627 |
rs7902627 | |
pharmgkb | rs7902627 |
gwascentral | rs7902627 |
openSNP | rs7902627 |
23andMe | rs7902627 |
SNPshot | rs7902627 |
SNPdbe | rs7902627 |
MSV3d | rs7902627 |
GWAS Ctlg | rs7902627 |
GMAF | 0.2052 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | .20 [0.11-0.29] unit decrease |