SNP Detail For rs2360806
1.Mapping Information
Human SNP ID rs2360806
Human chromosome chr8
Human SNP position 52213174
Pig chromosome chr4
Pig SNP position 85090194
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
Region8q11.23
Chromosome idchr8
Chromosome position52213174
Reported geneST18
Mapped geneST18
Upstream gene id
Downstream gene id
SNP gene ids9705
Upstream gene distance
Downstream gene distance
SNP risk allelers2360806-C
SNPsrs2360806
Merged0
SNP id current2360806
Contextintron_variant
Intergenic0
Allele frequency0.162
P value0.00000000007
Pvalue mlog10.1549019599857
P value text
Or beta0.047
%95 Ci[0.033-0.061] unit increase
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759