SNP Detail For rs4909945
1.Mapping Information
Human SNP ID rs4909945
Human chromosome chr11
Human SNP position 10652192
Pig chromosome chr2
Pig SNP position 52181840
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
Region11p15.4
Chromosome idchr11
Chromosome position10652192
Reported geneintergenic
Mapped geneMRVI1
Upstream gene id
Downstream gene id
SNP gene ids10335
Upstream gene distance
Downstream gene distance
SNP risk allelers4909945-?
SNPsrs4909945
Merged0
SNP id current4909945
Contextmissense_variant
Intergenic0
Allele frequency0.67
P value0.0000002
Pvalue mlog6.69897000433601
P value text
Or beta1.06
%95 Ci[1.04-1.09]
PlatformAffymetrix, Illumina [~ 2300000] (imputed)
CNVN
Mapped traitmigraine disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003821
Study accessionGCST002081