rs284924
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs284924(G;G) |
Make rs284924(G;T) |
Make rs284924(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 77009729 |
is a | snp |
is | mentioned by |
dbSNP | rs284924 |
dbSNP (classic) | rs284924 |
ClinGen | rs284924 |
ebi | rs284924 |
HLI | rs284924 |
Exac | rs284924 |
Gnomad | rs284924 |
Varsome | rs284924 |
LitVar | rs284924 |
Map | rs284924 |
PheGenI | rs284924 |
Biobank | rs284924 |
1000 genomes | rs284924 |
hgdp | rs284924 |
ensembl | rs284924 |
geneview | rs284924 |
scholar | rs284924 |
rs284924 | |
pharmgkb | rs284924 |
gwascentral | rs284924 |
openSNP | rs284924 |
23andMe | rs284924 |
SNPshot | rs284924 |
SNPdbe | rs284924 |
MSV3d | rs284924 |
GWAS Ctlg | rs284924 |
GMAF | 0.1873 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 23920401] Genetic variants in nuclear factor-kappa B binding sites are associated with clinical outcomes in prostate cancer patients