SNP Detail For rs7065696
1.Mapping Information
Human SNP ID rs7065696
Human chromosome chrX
Human SNP position 53947621
Pig chromosome chrX
Pig SNP position 52140673
2.Annotation Information
PubMed ID21057379
JournalPsychiatr Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/21057379
StudyCase-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.
Disease/TraitBipolar disorder and schizophrenia
Initial sample506 European ancestry bipolar 1 disorder cases, 523 European ancestry schizophrenia cases, 505 European ancestry controls
Replication sampleNA
RegionXp11.22
Chromosome idchrX
Chromosome position53947621
Reported genePHF8
Mapped genePHF8
Upstream gene id
Downstream gene id
SNP gene ids23133
Upstream gene distance
Downstream gene distance
SNP risk allelers7065696-?
SNPsrs7065696
Merged0
SNP id current7065696
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.0000004
Pvalue mlog6.39794000867203
P value text
Or beta
%95 Ci
PlatformAffymetrix [302482]
CNVN
Mapped traitmental or behavioural disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000677
Study accessionGCST000862