rs7830
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs7830(A;A) |
Make rs7830(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 151012483 |
Gene | ATG9B, NOS3 |
is a | snp |
is | mentioned by |
dbSNP | rs7830 |
dbSNP (classic) | rs7830 |
ClinGen | rs7830 |
ebi | rs7830 |
HLI | rs7830 |
Exac | rs7830 |
Gnomad | rs7830 |
Varsome | rs7830 |
LitVar | rs7830 |
Map | rs7830 |
PheGenI | rs7830 |
Biobank | rs7830 |
1000 genomes | rs7830 |
hgdp | rs7830 |
ensembl | rs7830 |
geneview | rs7830 |
scholar | rs7830 |
rs7830 | |
pharmgkb | rs7830 |
gwascentral | rs7830 |
openSNP | rs7830 |
23andMe | rs7830 |
SNPshot | rs7830 |
SNPdbe | rs7830 |
MSV3d | rs7830 |
GWAS Ctlg | rs7830 |
GMAF | 0.3632 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19815736] The Relation between Endothelial Nitric Oxide Synthase Gene Variants and Primary Open-Angle Glaucoma: Interactions with Gender and Postmenopausal Hormone Use
[PMID 21968727] Association of eNOS gene polymorphisms with essential hypertension in the Han population in southwestern China
[PMID 22025889] Reproductive factors and NOS3 variant interactions in primary open-angle glaucoma
[PMID 17367796] Association of polymorphisms in NOS3 with the ankle-brachial index in hypertensive adults.
[PMID 17980690] Polymorphisms in the endothelial nitric oxide synthase gene and bone density/ultrasound and geometry in humans.
[PMID 21245953] Association of genetic polymorphisms of eNOS with glaucoma.
[PMID 22368302] Single nucleotide polymorphisms in the NOS2 and NOS3 genes are associated with exhaled nitric oxide.
[PMID 22982457] eNOS gene polymorphisms modify the association of PM(10) with oxidative stress.
[PMID 23062210] eNOS tag SNP haplotypes in hypertensive disorders of pregnancy.
[PMID 23069892] Effects of endothelial nitric oxide synthase tagSNPs haplotypes on nitrite levels in black subjects.
[PMID 24085449] Polymorphisms in the endothelial nitric oxide synthase gene associated with recurrent miscarriage
[PMID 24938467] Genetic variants of the endothelial NO synthase gene (eNOS) may confer increased risk of sporadic congenital heart disease
[PMID 27706723] Association between functional polymorphisms in the nitric oxide synthase 3 gene and pediatric acute respiratory distress syndrome.
ClinVar | |
---|---|
Risk | rs7830(A;A) |
Alt | rs7830(A;A) |
Reference | Rs7830(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | NOS3 ATG9B |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000007.13:g.150709571G>T |
CLNSRC | |
CLNACC | RCV000455864.1, |