rs224278
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs224278(C;C) |
Make rs224278(C;T) |
Make rs224278(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 62820815 |
Gene | EGR2 |
is a | snp |
is | mentioned by |
dbSNP | rs224278 |
dbSNP (classic) | rs224278 |
ClinGen | rs224278 |
ebi | rs224278 |
HLI | rs224278 |
Exac | rs224278 |
Gnomad | rs224278 |
Varsome | rs224278 |
LitVar | rs224278 |
Map | rs224278 |
PheGenI | rs224278 |
Biobank | rs224278 |
1000 genomes | rs224278 |
hgdp | rs224278 |
ensembl | rs224278 |
geneview | rs224278 |
scholar | rs224278 |
rs224278 | |
pharmgkb | rs224278 |
gwascentral | rs224278 |
openSNP | rs224278 |
23andMe | rs224278 |
SNPshot | rs224278 |
SNPdbe | rs224278 |
MSV3d | rs224278 |
GWAS Ctlg | rs224278 |
GMAF | 0.449 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22327514] Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma