SNP Detail For rs997295
1.Mapping Information
Human SNP ID rs997295
Human chromosome chr15
Human SNP position 67724005
Pig chromosome chr1
Pig SNP position 183472937
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
Region15q23
Chromosome idchr15
Chromosome position67724005
Reported geneMAP2K5
Mapped geneMAP2K5
Upstream gene id
Downstream gene id
SNP gene ids5607
Upstream gene distance
Downstream gene distance
SNP risk allelers997295-T
SNPsrs997295
Merged0
SNP id current997295
Contextintron_variant
Intergenic0
Allele frequency0.588
P value0.000000003
Pvalue mlog8.52287874528033
P value text
Or beta0.033
%95 Ci[0.022-0.044] unit decrease
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759