SNP Detail For rs1858111
1.Mapping Information
Human SNP ID rs1858111
Human chromosome chr1
Human SNP position 95624175
Pig chromosome chr4
Pig SNP position 133665161
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
Region1p21.3
Chromosome idchr1
Chromosome position95624175
Reported geneRWDD3
Mapped geneLOC100996635 - LOC101928219
Upstream gene id100996635
Downstream gene id101928219
SNP gene ids
Upstream gene distance108711
Downstream gene distance1275
SNP risk allelers1858111-G
SNPsrs1858111
Merged0
SNP id current1858111
Contextintron_variant
Intergenic1
Allele frequency0.567
P value0.00000000000004
Pvalue mlog13.397940008672
P value text
Or beta0.039
%95 Ci[0.029-0.05] unit decrease
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759