SNP Detail For rs2556378
1.Mapping Information
Human SNP ID rs2556378
Human chromosome chr2
Human SNP position 60535367
Pig chromosome chr3
Pig SNP position 85302328
2.Annotation Information
PubMed ID22012869
JournalAm J Med Genet B Neuropsychiatr Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/22012869
StudyGenome-wide association study in German patients with attention deficit/hyperactivity disorder.
Disease/TraitAttention deficit hyperactivity disorder
Initial sample495 European ancestry child and adolescent cases, 1,300 European ancestry adult controls
Replication sample1,023 European ancestry individuals from 320 families, 2455 European ancestry cases and 896 European ancestry controls from 2,064 trios
Region2p16.1
Chromosome idchr2
Chromosome position60535367
Reported geneBCL11A
Mapped geneBCL11A
Upstream gene id
Downstream gene id
SNP gene ids53335
Upstream gene distance
Downstream gene distance
SNP risk allelers2556378-T
SNPsrs2556378
Merged0
SNP id current2556378
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000007
Pvalue mlog5.15490195998574
P value text
Or beta
%95 Ci
PlatformIllumina [487484]
CNVN
Mapped traitattention deficit hyperactivity disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003888
Study accessionGCST001287