rs3918188

Orientation

plus

Stabilized

plus

Make rs3918188(A;A)

Make rs3918188(A;C)

Make rs3918188(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

151005693

Gene

NOS3

is a	snp
is	mentioned by
dbSNP	rs3918188
dbSNP (classic)	rs3918188
ClinGen	rs3918188
ebi	rs3918188
HLI	rs3918188
Exac	rs3918188
Gnomad	rs3918188
Varsome	rs3918188
LitVar	rs3918188
Map	rs3918188
PheGenI	rs3918188
Biobank	rs3918188
1000 genomes	rs3918188
hgdp	rs3918188
ensembl	rs3918188
geneview	rs3918188
scholar	rs3918188
google	rs3918188
pharmgkb	rs3918188
gwascentral	rs3918188
openSNP	rs3918188
23andMe	rs3918188
SNPshot	rs3918188
SNPdbe	rs3918188
MSV3d	rs3918188
GWAS Ctlg	rs3918188

GMAF

0.2998

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 22025889 ] Reproductive factors and NOS3 variant interactions in primary open-angle glaucoma

[PMID 17980690 ] Polymorphisms in the endothelial nitric oxide synthase gene and bone density/ultrasound and geometry in humans.

[PMID 18246059 ] Habitual energy expenditure modifies the association between NOS3 gene polymorphisms and blood pressure.

[PMID 21245953 ] Association of genetic polymorphisms of eNOS with glaucoma.

[PMID 21674837 ] Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.

[PMID 23069892] Effects of endothelial nitric oxide synthase tagSNPs haplotypes on nitrite levels in black subjects.

[PMID 24047197] Endothelial nitric oxide synthase gene variants and haplotypes associated with an increased risk of idiopathic recurrent miscarriage

[PMID 24085449] Polymorphisms in the endothelial nitric oxide synthase gene associated with recurrent miscarriage

[PMID 27706723] Association between functional polymorphisms in the nitric oxide synthase 3 gene and pediatric acute respiratory distress syndrome.