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rs6057652

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common genotype
Make rs6057652(A;C)
Make rs6057652(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position32832003
GeneMAPRE1
is asnp
is mentioned by
dbSNPrs6057652
dbSNP (classic)rs6057652
ClinGenrs6057652
ebirs6057652
HLIrs6057652
Exacrs6057652
Gnomadrs6057652
Varsomers6057652
LitVarrs6057652
Maprs6057652
PheGenIrs6057652
Biobankrs6057652
1000 genomesrs6057652
hgdprs6057652
ensemblrs6057652
geneviewrs6057652
scholarrs6057652
googlers6057652
pharmgkbrs6057652
gwascentralrs6057652
openSNPrs6057652
23andMers6057652
SNPshotrs6057652
SNPdbers6057652
MSV3drs6057652
GWAS Ctlgrs6057652
GMAF0.01148
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 23527680]
Trait Attention deficit hyperactivity disorder (combined symptoms)
Title Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele A
P-val 4E-6
Odds Ratio NR NR