SNP Detail For rs6946969
1.Mapping Information
Human SNP ID rs6946969
Human chromosome chr7
Human SNP position 70746041
Pig chromosome chr3
Pig SNP position 14900376
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
Region7q11.22
Chromosome idchr7
Chromosome position70746041
Reported geneAUTS2
Mapped geneLOC105375347, AUTS2
Upstream gene id
Downstream gene id
SNP gene ids105375347, 26053
Upstream gene distance
Downstream gene distance
SNP risk allelers6946969-G
SNPsrs6946969
Merged0
SNP id current6946969
Contextintron_variant
Intergenic0
Allele frequency0.658
P value0.000000002
Pvalue mlog8.69897000433601
P value text
Or beta0.033
%95 Ci[0.022-0.043] unit increase
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759