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rs478597

From SNPedia

Orientationminus
Stabilizedminus
Make rs478597(C;C)
Make rs478597(C;T)
Make rs478597(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position117313620
GeneNOS1
is asnp
is mentioned by
dbSNPrs478597
ebirs478597
HLIrs478597
Exacrs478597
Varsomers478597
Maprs478597
PheGenIrs478597
hapmaprs478597
1000 genomesrs478597
hgdprs478597
ensemblrs478597
gopubmedrs478597
geneviewrs478597
scholarrs478597
googlers478597
pharmgkbrs478597
gwascentralrs478597
openSNPrs478597
23andMers478597
23andMe allrs478597
SNP Nexus

SNPshotrs478597
SNPdbers478597
MSV3drs478597
GWAS Ctlgrs478597
GMAF0.3104
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18821565]
Trait Inattentive symptoms
Title Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations
Risk Allele
P-val 0.000008
Odds Ratio NR NR

[PMID 18663495OA-icon.png] Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.

GET Evidence
rs478597
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary