rs11160707
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11160707(A;A) |
Make rs11160707(A;G) |
Make rs11160707(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 14 |
Position | 102908373 |
Gene | TRAF3 |
is a | snp |
is | mentioned by |
dbSNP | rs11160707 |
dbSNP (classic) | rs11160707 |
ClinGen | rs11160707 |
ebi | rs11160707 |
HLI | rs11160707 |
Exac | rs11160707 |
Gnomad | rs11160707 |
Varsome | rs11160707 |
LitVar | rs11160707 |
Map | rs11160707 |
PheGenI | rs11160707 |
Biobank | rs11160707 |
1000 genomes | rs11160707 |
hgdp | rs11160707 |
ensembl | rs11160707 |
geneview | rs11160707 |
scholar | rs11160707 |
rs11160707 | |
pharmgkb | rs11160707 |
gwascentral | rs11160707 |
openSNP | rs11160707 |
23andMe | rs11160707 |
SNPshot | rs11160707 |
SNPdbe | rs11160707 |
MSV3d | rs11160707 |
GWAS Ctlg | rs11160707 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26919710] Variations in genes involved in regulation of the nuclear factor - κB pathway and the risk of acute myeloid leukaemia.