SNP Detail For rs183823891
1.Mapping Information
Human SNP ID rs183823891
Human chromosome chr2
Human SNP position 25129331
Pig chromosome chr3
Pig SNP position 120798800
2.Annotation Information
PubMed ID26198764
JournalAm J Med Genet B Neuropsychiatr Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/26198764
StudyGenome-wide association study of schizophrenia in Ashkenazi Jews.
Disease/TraitSchizophrenia
Initial sample592 Ashkenazi Jewish ancestry cases, 505 Ashkenazi Jewish ancestry controls, 36,989 cases, 113,075 controls
Replication sampleNA
Region2p23.3
Chromosome idchr2
Chromosome position25129331
Reported geneNR
Mapped geneEFR3B
Upstream gene id
Downstream gene id
SNP gene ids22979
Upstream gene distance
Downstream gene distance
SNP risk allelers183823891-T
SNPsrs183823891
Merged
SNP id current183823891
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.0000001
Pvalue mlog7
P value text
Or beta1.07
%95 Ci[NR]
PlatformIllumina [7158791] (imputed)
CNVN
Mapped traitschizophrenia
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000692
Study accessionGCST003048