SNP Detail For rs12355831
1.Mapping Information
Human SNP ID rs12355831
Human chromosome chr10
Human SNP position 112442768
Pig chromosome chr14
Pig SNP position 133768486
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
Region10q25.2
Chromosome idchr10
Chromosome position112442768
Reported geneintergenic
Mapped geneZDHHC6
Upstream gene id
Downstream gene id
SNP gene ids64429
Upstream gene distance
Downstream gene distance
SNP risk allelers12355831-G
SNPsrs12355831
Merged0
SNP id current12355831
Contextintron_variant
Intergenic0
Allele frequency0.11
P value0.000002
Pvalue mlog5.69897000433601
P value text
Or beta1.09
%95 Ci[1.05-1.14]
PlatformAffymetrix, Illumina [~ 2300000] (imputed)
CNVN
Mapped traitmigraine disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003821
Study accessionGCST002081