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rs41279104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41279104(C;T)
Make rs41279104(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position117439680
GeneNOS1
is asnp
is mentioned by
dbSNPrs41279104
ebirs41279104
HLIrs41279104
Exacrs41279104
Varsomers41279104
Maprs41279104
PheGenIrs41279104
hapmaprs41279104
1000 genomesrs41279104
hgdprs41279104
ensemblrs41279104
gopubmedrs41279104
geneviewrs41279104
scholarrs41279104
googlers41279104
pharmgkbrs41279104
gwascentralrs41279104
openSNPrs41279104
23andMers41279104
23andMe allrs41279104
SNP Nexus

SNPshotrs41279104
SNPdbers41279104
MSV3drs41279104
GWAS Ctlgrs41279104
GMAF0.124
Max Magnitude0

[PMID 19513863] No association between polymorphisms of neuronal oxide synthase 1 gene (NOS1) and schizophrenia in a Japanese population

[PMID 19851341] No association between a promoter NOS1 polymorphism (rs41279104) and Infantile Hypertrophic Pyloric Stenosis

[PMID 20470850] A common polymorphism in the 3'-UTR of the NOS1 gene was associated with completed suicides in Japanese male population

[PMID 20605417] A putative cis-acting polymorphism in the NOS1 gene is associated with schizophrenia and NOS1 immunoreactivity in the postmortem brain

OMIM163731
DescNITRIC OXIDE SYNTHASE 1; NOS1
Variant
Relatedalso

[PMID 21281558] A functional promoter polymorphism of neuronal nitric oxide synthase moderates prefrontal functioning in schizophrenia

OMIM163731
Desc
Variant0001
Relatedalso
OMIM179010
Desc
Variant
Relatedalso
[PMID 20016223] Genetic association analysis of functional polymorphisms in neuronal nitric oxide synthase 1 gene (NOS1) and mood disorders and fluvoxamine response in major depressive disorder in the Japanese population.

[PMID 24220657] The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia: Further evidence and meta-analysis [PMID 23826716] Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis.

ClinVar
Risk rs41279104(T;T)
Alt rs41279104(T;T)
Reference rs41279104(C;C)
Significance Unknown
Disease Pyloric stenosis
Variation info
Gene NOS1
CLNDBN Pyloric stenosis, infantile hypertrophic 1
Reversed 0
HGVS NC_000012.11:g.117877485C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015050.2,