rs7101378
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7101378(A;A) |
Make rs7101378(A;G) |
Make rs7101378(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 109022640 |
is a | snp |
is | mentioned by |
dbSNP | rs7101378 |
dbSNP (classic) | rs7101378 |
ClinGen | rs7101378 |
ebi | rs7101378 |
HLI | rs7101378 |
Exac | rs7101378 |
Gnomad | rs7101378 |
Varsome | rs7101378 |
LitVar | rs7101378 |
Map | rs7101378 |
PheGenI | rs7101378 |
Biobank | rs7101378 |
1000 genomes | rs7101378 |
hgdp | rs7101378 |
ensembl | rs7101378 |
geneview | rs7101378 |
scholar | rs7101378 |
rs7101378 | |
pharmgkb | rs7101378 |
gwascentral | rs7101378 |
openSNP | rs7101378 |
23andMe | rs7101378 |
SNPshot | rs7101378 |
SNPdbe | rs7101378 |
MSV3d | rs7101378 |
GWAS Ctlg | rs7101378 |
GMAF | 0.3388 |
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 | G |
P-val | 7E-6 |
Odds Ratio | .14 [0.079-0.201] unit increase |