SNP Detail For rs11750092
1.Mapping Information
Human SNP ID rs11750092
Human chromosome chr5
Human SNP position 159940964
Pig chromosome chr16
Pig SNP position 69068362
2.Annotation Information
PubMed ID23793025
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23793025
StudyGenome-wide meta-analysis identifies new susceptibility loci for migraine.
Disease/TraitMigraine
Initial sample23,285 European ancestry cases, 95,425 European ancestry controls
Replication sampleNA
Region5q33.3
Chromosome idchr5
Chromosome position159940964
Reported geneintergenic
Mapped geneADRA1B
Upstream gene id
Downstream gene id
SNP gene ids147
Upstream gene distance
Downstream gene distance
SNP risk allelers11750092-T
SNPsrs11750092
Merged0
SNP id current11750092
Contextintron_variant
Intergenic0
Allele frequency0.16
P value0.000007
Pvalue mlog5.15490195998574
P value text
Or beta1.07
%95 Ci[1.04-1.11]
PlatformAffymetrix, Illumina [~ 2300000] (imputed)
CNVN
Mapped traitmigraine disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003821
Study accessionGCST002081