SNP Detail For rs17600642
1.Mapping Information
Human SNP ID rs17600642
Human chromosome chr10
Human SNP position 70703238
Pig chromosome chr14
Pig SNP position 79440707
2.Annotation Information
PubMed ID21254220
JournalGenet Epidemiol
Linkwww.ncbi.nlm.nih.gov/pubmed/21254220
StudyPropensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Disease/TraitBipolar disorder
Initial sample1,868 European ancestry cases, 2,938 European ancestry controls
Replication sampleNA
Region10q22.1
Chromosome idchr10
Chromosome position70703238
Reported geneNR
Mapped geneADAMTS14
Upstream gene id
Downstream gene id
SNP gene ids140766
Upstream gene distance
Downstream gene distance
SNP risk allelers17600642-?
SNPsrs17600642
Merged0
SNP id current17600642
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000005
Pvalue mlog5.30102999566398
P value text(addtive)
Or beta
%95 Ci
PlatformAffymetrix [NR]
CNVN
Mapped traitbipolar disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000289
Study accessionGCST000961