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rs12926729

From SNPedia

Orientationplus
Stabilizedplus
Make rs12926729(A;A)
Make rs12926729(A;G)
Make rs12926729(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position20089048
is asnp
is mentioned by
dbSNPrs12926729
ebirs12926729
HLIrs12926729
Exacrs12926729
Varsomers12926729
Maprs12926729
PheGenIrs12926729
hapmaprs12926729
1000 genomesrs12926729
hgdprs12926729
ensemblrs12926729
gopubmedrs12926729
geneviewrs12926729
scholarrs12926729
googlers12926729
pharmgkbrs12926729
gwascentralrs12926729
openSNPrs12926729
23andMers12926729
23andMe allrs12926729
SNP Nexus

SNPshotrs12926729
SNPdbers12926729
MSV3drs12926729
GWAS Ctlgrs12926729
GMAF0.1892
Max Magnitude
? (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 7E-6
Odds Ratio NR NR