rs2779248
From SNPedia
Orientation | plus |
Make rs2779248(C;C) |
Make rs2779248(C;T) |
Make rs2779248(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 17 |
Position | 27800806 |
Gene | NOS2 |
is a | snp |
is | mentioned by |
dbSNP | rs2779248 |
dbSNP (classic) | rs2779248 |
ClinGen | rs2779248 |
ebi | rs2779248 |
HLI | rs2779248 |
Exac | rs2779248 |
Gnomad | rs2779248 |
Varsome | rs2779248 |
LitVar | rs2779248 |
Map | rs2779248 |
PheGenI | rs2779248 |
Biobank | rs2779248 |
1000 genomes | rs2779248 |
hgdp | rs2779248 |
ensembl | rs2779248 |
geneview | rs2779248 |
scholar | rs2779248 |
rs2779248 | |
pharmgkb | rs2779248 |
gwascentral | rs2779248 |
openSNP | rs2779248 |
23andMe | rs2779248 |
SNPshot | rs2779248 |
SNPdbe | rs2779248 |
MSV3d | rs2779248 |
GWAS Ctlg | rs2779248 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 30581791] Nitric Oxide Synthase 2 Polymorphisms (rs2779248T/C and rs1137933C/T) and the Risk of Type 2 Diabetes in Zahedan, Southeastern Iran.