rs2677247
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2677247(G;G) |
Make rs2677247(G;T) |
Make rs2677247(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 103731747 |
is a | snp |
is | mentioned by |
dbSNP | rs2677247 |
dbSNP (classic) | rs2677247 |
ClinGen | rs2677247 |
ebi | rs2677247 |
HLI | rs2677247 |
Exac | rs2677247 |
Gnomad | rs2677247 |
Varsome | rs2677247 |
LitVar | rs2677247 |
Map | rs2677247 |
PheGenI | rs2677247 |
Biobank | rs2677247 |
1000 genomes | rs2677247 |
hgdp | rs2677247 |
ensembl | rs2677247 |
geneview | rs2677247 |
scholar | rs2677247 |
rs2677247 | |
pharmgkb | rs2677247 |
gwascentral | rs2677247 |
openSNP | rs2677247 |
23andMe | rs2677247 |
SNPshot | rs2677247 |
SNPdbe | rs2677247 |
MSV3d | rs2677247 |
GWAS Ctlg | rs2677247 |
GMAF | 0.3678 |
Max Magnitude | 0 |
? | (G;G) (G;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 | 9E-6 |
Odds Ratio | .14 [0.079-0.204] unit decrease |