rs2779249
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2779249(A;A) |
Make rs2779249(A;C) |
Make rs2779249(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 27801555 |
Gene | NOS2 |
is a | snp |
is | mentioned by |
dbSNP | rs2779249 |
dbSNP (classic) | rs2779249 |
ClinGen | rs2779249 |
ebi | rs2779249 |
HLI | rs2779249 |
Exac | rs2779249 |
Gnomad | rs2779249 |
Varsome | rs2779249 |
LitVar | rs2779249 |
Map | rs2779249 |
PheGenI | rs2779249 |
Biobank | rs2779249 |
1000 genomes | rs2779249 |
hgdp | rs2779249 |
ensembl | rs2779249 |
geneview | rs2779249 |
scholar | rs2779249 |
rs2779249 | |
pharmgkb | rs2779249 |
gwascentral | rs2779249 |
openSNP | rs2779249 |
23andMe | rs2779249 |
SNPshot | rs2779249 |
SNPdbe | rs2779249 |
MSV3d | rs2779249 |
GWAS Ctlg | rs2779249 |
GMAF | 0.2626 |
Max Magnitude | 0 |
[PMID 21716319] Maternal iNOS genetic polymorphisms and hypertensive disorders of pregnancy
[PMID 22234503] Inducible nitric oxide synthase haplotype associated with migraine and aura
[PMID 19147409] Investigation of chromosome 17 candidate genes in susceptibility to TB in a South African population.
[PMID 22588838] The apoptosis pathway and the genetic predisposition to Achilles tendinopathy.
[PMID 22865486] Interaction among nitric oxide (NO)-related genes in migraine susceptibility.
[PMID 26579803] Functional Inducible Nitric Oxide Synthase Gene Variants Associate With Hypertension: A Case-Control Study in a Finnish Population-The TAMRISK Study