SNP Detail For rs11168351
1.Mapping Information
Human SNP ID rs11168351
Human chromosome chr12
Human SNP position 48009982
Pig chromosome chr5
Pig SNP position 81560153
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
Region12q13.11
Chromosome idchr12
Chromosome position48009982
Reported geneNR
Mapped geneCOL2A1
Upstream gene id
Downstream gene id
SNP gene ids1280
Upstream gene distance
Downstream gene distance
SNP risk allelers11168351-?
SNPsrs11168351
Merged0
SNP id current11168351
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000009
Pvalue mlog5.04575749056067
P value text
Or beta1.2231
%95 Ci[NR]
PlatformAffymetrix [722112]
CNVN
Mapped traitmental or behavioural disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000677
Study accessionGCST000821