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rs11790994

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11790994(C;G)
Make rs11790994(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position95666984
is asnp
is mentioned by
dbSNPrs11790994
ebirs11790994
HLIrs11790994
Exacrs11790994
Varsomers11790994
Maprs11790994
PheGenIrs11790994
hapmaprs11790994
1000 genomesrs11790994
hgdprs11790994
ensemblrs11790994
gopubmedrs11790994
geneviewrs11790994
scholarrs11790994
googlers11790994
pharmgkbrs11790994
gwascentralrs11790994
openSNPrs11790994
23andMers11790994
23andMe allrs11790994
SNP Nexus

SNPshotrs11790994
SNPdbers11790994
MSV3drs11790994
GWAS Ctlgrs11790994
GMAF0.1015
Max Magnitude0
? (C;C) (C;G) (G;G) 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 2E-7
Odds Ratio NR NR


GET Evidence
rs11790994
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary