SNP Detail For rs1042992
1.Mapping Information
Human SNP ID rs1042992
Human chromosome chr8
Human SNP position 26411675
Pig chromosome chr14
Pig SNP position 11509316
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
Region8p21.2
Chromosome idchr8
Chromosome position26411675
Reported geneNR
Mapped geneBNIP3L
Upstream gene id
Downstream gene id
SNP gene ids665
Upstream gene distance
Downstream gene distance
SNP risk allelers1042992-T
SNPsrs1042992
Merged
SNP id current1042992
Context3_prime_UTR_variant
Intergenic0
Allele frequencyNR
P value0.0000002
Pvalue mlog6.69897000433601
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