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rs11590090

From SNPedia

Orientationplus
Stabilizedplus
Make rs11590090(A;A)
Make rs11590090(A;C)
Make rs11590090(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position112770941
is asnp
is mentioned by
dbSNPrs11590090
ebirs11590090
HLIrs11590090
Exacrs11590090
Varsomers11590090
Maprs11590090
PheGenIrs11590090
hapmaprs11590090
1000 genomesrs11590090
hgdprs11590090
ensemblrs11590090
gopubmedrs11590090
geneviewrs11590090
scholarrs11590090
googlers11590090
pharmgkbrs11590090
gwascentralrs11590090
openSNPrs11590090
23andMers11590090
23andMe allrs11590090
SNP Nexus

SNPshotrs11590090
SNPdbers11590090
MSV3drs11590090
GWAS Ctlgrs11590090
GMAF0.2043
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 18821565]
Trait Hyperactive-impulsive 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 0.000003
Odds Ratio NR NR


GET Evidence
rs11590090
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.242188
summary