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rs13006237

From SNPedia

Orientationplus
Stabilizedplus
Make rs13006237(A;A)
Make rs13006237(A;G)
Make rs13006237(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position123757465
is asnp
is mentioned by
dbSNPrs13006237
dbSNP (classic)rs13006237
ClinGenrs13006237
ebirs13006237
HLIrs13006237
Exacrs13006237
Gnomadrs13006237
Varsomers13006237
LitVarrs13006237
Maprs13006237
PheGenIrs13006237
Biobankrs13006237
1000 genomesrs13006237
hgdprs13006237
ensemblrs13006237
geneviewrs13006237
scholarrs13006237
googlers13006237
pharmgkbrs13006237
gwascentralrs13006237
openSNPrs13006237
23andMers13006237
SNPshotrs13006237
SNPdbers13006237
MSV3drs13006237
GWAS Ctlgrs13006237
GMAF0.1318
Max Magnitude0
? (A;A) (A;G) (G;G) 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 9E-6
Odds Ratio NR NR