SNP Detail For rs6057652
1.Mapping Information
Human SNP ID rs6057652
Human chromosome chr20
Human SNP position 32832003
Pig chromosome chr17
Pig SNP position 41341431
2.Annotation Information
PubMed ID23527680
JournalTwin Res Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23527680
StudyGenome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Disease/TraitAttention deficit hyperactivity disorder (combined symptoms)
Initial sample1,851 individuals
Replication sample155 individuals
Region20q11.21
Chromosome idchr20
Chromosome position32832003
Reported geneNR
Mapped geneMAPRE1
Upstream gene id
Downstream gene id
SNP gene ids22919
Upstream gene distance
Downstream gene distance
SNP risk allelers6057652-A
SNPsrs6057652
Merged0
SNP id current6057652
Contextintron_variant
Intergenic0
Allele frequency
P value0.000004
Pvalue mlog5.39794000867203
P value text
Or beta
%95 Ci
PlatformIllumina [2373249] (imputed)
CNVN
Mapped traitattention deficit hyperactivity disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003888
Study accessionGCST001931
PubMed ID23527680
JournalTwin Res Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23527680
StudyGenome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Disease/TraitAttention deficit hyperactivity disorder (hyperactivity-impulsivity symptoms)
Initial sample1,851 individuals
Replication sample155 individuals
Region20q11.21
Chromosome idchr20
Chromosome position32832003
Reported geneNR
Mapped geneMAPRE1
Upstream gene id
Downstream gene id
SNP gene ids22919
Upstream gene distance
Downstream gene distance
SNP risk allelers6057652-A
SNPsrs6057652
Merged0
SNP id current6057652
Contextintron_variant
Intergenic0
Allele frequency
P value0.000007
Pvalue mlog5.15490195998574
P value text
Or beta
%95 Ci
PlatformIllumina [2373249] (imputed)
CNVN
Mapped traitattention deficit hyperactivity disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003888
Study accessionGCST001944