SNP Detail For rs17766408
1.Mapping Information
Human SNP ID rs17766408
Human chromosome chr12
Human SNP position 65791310
Pig chromosome JH118649-1
Pig SNP position 264899
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
Region12q14.3
Chromosome idchr12
Chromosome position65791310
Reported geneNR
Mapped geneRPSAP52
Upstream gene id
Downstream gene id
SNP gene ids204010
Upstream gene distance
Downstream gene distance
SNP risk allelers17766408-T
SNPsrs17766408
Merged
SNP id current17766408
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000004
Pvalue mlog5.39794000867203
P value text
Or beta1.08
%95 Ci[NR]
PlatformIllumina [7158791] (imputed)
CNVN
Mapped traitschizophrenia
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000692
Study accessionGCST003048