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rs7448069

From SNPedia

Orientationplus
Stabilizedplus
Make rs7448069(C;C)
Make rs7448069(C;T)
Make rs7448069(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position175817031
GeneCPLX2
is asnp
is mentioned by
dbSNPrs7448069
ebirs7448069
HLIrs7448069
Exacrs7448069
Varsomers7448069
Maprs7448069
PheGenIrs7448069
hapmaprs7448069
1000 genomesrs7448069
hgdprs7448069
ensemblrs7448069
gopubmedrs7448069
geneviewrs7448069
scholarrs7448069
googlers7448069
pharmgkbrs7448069
gwascentralrs7448069
openSNPrs7448069
23andMers7448069
23andMe allrs7448069
SNP Nexus

SNPshotrs7448069
SNPdbers7448069
MSV3drs7448069
GWAS Ctlgrs7448069
GMAF0.02663
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 1E-6
Odds Ratio NR NR