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rs2779249

From SNPedia

Orientationplus
Stabilizedplus
Make rs2779249(A;A)
Make rs2779249(A;C)
Make rs2779249(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position27801555
GeneNOS2
is asnp
is mentioned by
dbSNPrs2779249
ebirs2779249
HLIrs2779249
Exacrs2779249
Varsomers2779249
Maprs2779249
PheGenIrs2779249
hapmaprs2779249
1000 genomesrs2779249
hgdprs2779249
ensemblrs2779249
gopubmedrs2779249
geneviewrs2779249
scholarrs2779249
googlers2779249
pharmgkbrs2779249
gwascentralrs2779249
openSNPrs2779249
23andMers2779249
23andMe allrs2779249
SNP Nexus

SNPshotrs2779249
SNPdbers2779249
MSV3drs2779249
GWAS Ctlgrs2779249
GMAF0.2626
Max Magnitude

[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 26579803OA-icon.png] Functional Inducible Nitric Oxide Synthase Gene Variants Associate With Hypertension: A Case-Control Study in a Finnish Population-The TAMRISK Study