rs9430161
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9430161(G;G) |
Make rs9430161(G;T) |
Make rs9430161(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 10986798 |
Gene | LOC390996 |
is a | snp |
is | mentioned by |
dbSNP | rs9430161 |
dbSNP (classic) | rs9430161 |
ClinGen | rs9430161 |
ebi | rs9430161 |
HLI | rs9430161 |
Exac | rs9430161 |
Gnomad | rs9430161 |
Varsome | rs9430161 |
LitVar | rs9430161 |
Map | rs9430161 |
PheGenI | rs9430161 |
Biobank | rs9430161 |
1000 genomes | rs9430161 |
hgdp | rs9430161 |
ensembl | rs9430161 |
geneview | rs9430161 |
scholar | rs9430161 |
rs9430161 | |
pharmgkb | rs9430161 |
gwascentral | rs9430161 |
openSNP | rs9430161 |
23andMe | rs9430161 |
SNPshot | rs9430161 |
SNPdbe | rs9430161 |
MSV3d | rs9430161 |
GWAS Ctlg | rs9430161 |
GMAF | 0.2351 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 22327514] Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma