SNP Detail For rs134882
1.Mapping Information
Human SNP ID rs134882
Human chromosome chr22
Human SNP position 42274959
Pig chromosome chr5
Pig SNP position 4081571
2.Annotation Information
PubMed ID20889312
JournalSchizophr Res
Linkwww.ncbi.nlm.nih.gov/pubmed/20889312
StudyA genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
Disease/TraitBipolar disorder and schizophrenia
Initial sample651 European ancestry bipolar cases, 1,171 European ancestry schizophrenia cases, 2,412 European ancestry controls
Replication sampleNA
Region22q13.2
Chromosome idchr22
Chromosome position42274959
Reported geneNR
Mapped geneTCF20
Upstream gene id
Downstream gene id
SNP gene ids6942
Upstream gene distance
Downstream gene distance
SNP risk allelers134882-?
SNPsrs134882
Merged0
SNP id current134882
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000007
Pvalue mlog5.15490195998574
P value text
Or beta1.2196
%95 Ci[NR]
PlatformAffymetrix [722112]
CNVN
Mapped traitmental or behavioural disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000677
Study accessionGCST000821