rs11785599
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11785599(C;C) |
Make rs11785599(C;T) |
Make rs11785599(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 23034761 |
Gene | TNFRSF10B |
is a | snp |
is | mentioned by |
dbSNP | rs11785599 |
dbSNP (classic) | rs11785599 |
ClinGen | rs11785599 |
ebi | rs11785599 |
HLI | rs11785599 |
Exac | rs11785599 |
Gnomad | rs11785599 |
Varsome | rs11785599 |
LitVar | rs11785599 |
Map | rs11785599 |
PheGenI | rs11785599 |
Biobank | rs11785599 |
1000 genomes | rs11785599 |
hgdp | rs11785599 |
ensembl | rs11785599 |
geneview | rs11785599 |
scholar | rs11785599 |
rs11785599 | |
pharmgkb | rs11785599 |
gwascentral | rs11785599 |
openSNP | rs11785599 |
23andMe | rs11785599 |
SNPshot | rs11785599 |
SNPdbe | rs11785599 |
MSV3d | rs11785599 |
GWAS Ctlg | rs11785599 |
GMAF | 0.3825 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23839018] TNFRSF10B polymorphisms and haplotypes associated with increased risk of death in non-small cell lung cancer