rs9295740
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9295740(A;A) |
Make rs9295740(A;G) |
Make rs9295740(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 27721723 |
Gene | TRNAL16 |
is a | snp |
is | mentioned by |
dbSNP | rs9295740 |
dbSNP (classic) | rs9295740 |
ClinGen | rs9295740 |
ebi | rs9295740 |
HLI | rs9295740 |
Exac | rs9295740 |
Gnomad | rs9295740 |
Varsome | rs9295740 |
LitVar | rs9295740 |
Map | rs9295740 |
PheGenI | rs9295740 |
Biobank | rs9295740 |
1000 genomes | rs9295740 |
hgdp | rs9295740 |
ensembl | rs9295740 |
geneview | rs9295740 |
scholar | rs9295740 |
rs9295740 | |
pharmgkb | rs9295740 |
gwascentral | rs9295740 |
openSNP | rs9295740 |
23andMe | rs9295740 |
SNPshot | rs9295740 |
SNPdbe | rs9295740 |
MSV3d | rs9295740 |
GWAS Ctlg | rs9295740 |
GMAF | 0.2691 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 22404340] Replication of results of genome-wide association studies on lung cancer susceptibility loci in a Korean population
[PMID 17903294] Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.
[PMID 18978787] Common 5p15.33 and 6p21.33 variants influence lung cancer risk.
[PMID 24039754] The impact of polymorphic variations in the 5p15, 6p12, 6p21 and 15q25 Loci on the risk and prognosis of portuguese patients with non-small cell lung cancer