rs9557635
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9557635(A;A) |
Make rs9557635(A;G) |
Make rs9557635(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 101398739 |
Gene | NALCN |
is a | snp |
is | mentioned by |
dbSNP | rs9557635 |
dbSNP (classic) | rs9557635 |
ClinGen | rs9557635 |
ebi | rs9557635 |
HLI | rs9557635 |
Exac | rs9557635 |
Gnomad | rs9557635 |
Varsome | rs9557635 |
LitVar | rs9557635 |
Map | rs9557635 |
PheGenI | rs9557635 |
Biobank | rs9557635 |
1000 genomes | rs9557635 |
hgdp | rs9557635 |
ensembl | rs9557635 |
geneview | rs9557635 |
scholar | rs9557635 |
rs9557635 | |
pharmgkb | rs9557635 |
gwascentral | rs9557635 |
openSNP | rs9557635 |
23andMe | rs9557635 |
SNPshot | rs9557635 |
SNPdbe | rs9557635 |
MSV3d | rs9557635 |
GWAS Ctlg | rs9557635 |
GMAF | 0.2309 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23144319] |
Trait | Non-small cell lung cancer |
Title | Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study. |
Risk Allele | A |
P-val | 9E-6 |
Odds Ratio | NR NR |