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rs11647507

From SNPedia

Orientationplus
Stabilizedplus
Make rs11647507(A;A)
Make rs11647507(A;C)
Make rs11647507(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position20084306
is asnp
is mentioned by
dbSNPrs11647507
ebirs11647507
HLIrs11647507
Exacrs11647507
Varsomers11647507
Maprs11647507
PheGenIrs11647507
hapmaprs11647507
1000 genomesrs11647507
hgdprs11647507
ensemblrs11647507
gopubmedrs11647507
geneviewrs11647507
scholarrs11647507
googlers11647507
pharmgkbrs11647507
gwascentralrs11647507
openSNPrs11647507
23andMers11647507
23andMe allrs11647507
SNP Nexus

SNPshotrs11647507
SNPdbers11647507
MSV3drs11647507
GWAS Ctlgrs11647507
GMAF0.2039
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23527680]
Trait Attention deficit hyperactivity disorder (inattention symptoms)
Title Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele A
P-val 7E-6
Odds Ratio NR NR