rs16949
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16949(C;C) |
Make rs16949(C;T) |
Make rs16949(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 27797673 |
Gene | NOS2 |
is a | snp |
is | mentioned by |
dbSNP | rs16949 |
dbSNP (classic) | rs16949 |
ClinGen | rs16949 |
ebi | rs16949 |
HLI | rs16949 |
Exac | rs16949 |
Gnomad | rs16949 |
Varsome | rs16949 |
LitVar | rs16949 |
Map | rs16949 |
PheGenI | rs16949 |
Biobank | rs16949 |
1000 genomes | rs16949 |
hgdp | rs16949 |
ensembl | rs16949 |
geneview | rs16949 |
scholar | rs16949 |
rs16949 | |
pharmgkb | rs16949 |
gwascentral | rs16949 |
openSNP | rs16949 |
23andMe | rs16949 |
SNPshot | rs16949 |
SNPdbe | rs16949 |
MSV3d | rs16949 |
GWAS Ctlg | rs16949 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24746566] Genetic variants in inducible nitric oxide synthase gene are associated with the risk of radiation-induced lung injury in lung cancer patients receiving definitive thoracic radiation