SNP Detail For rs9906289
1.Mapping Information
Human SNP ID rs9906289
Human chromosome chr17
Human SNP position 48567315
Pig chromosome chr12
Pig SNP position 24778739
2.Annotation Information
PubMed ID25628336
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25628336
StudyGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.
Disease/TraitMotion sickness
Initial sample80,494 European ancestry individuals
Replication sampleNA
Region17q21.32
Chromosome idchr17
Chromosome position48567315
Reported geneHOXB
Mapped geneHOXB3
Upstream gene id
Downstream gene id
SNP gene ids3213
Upstream gene distance
Downstream gene distance
SNP risk allelers9906289-T
SNPsrs9906289
Merged0
SNP id current9906289
Contextintron_variant
Intergenic0
Allele frequency0.046
P value0.00000000006
Pvalue mlog10.2218487496163
P value text
Or beta0.083
%95 Ci[0.058-0.108] unit increase
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759