SNP Detail For rs10514168
1.Mapping Information
Human SNP ID rs10514168
Human chromosome chr18
Human SNP position 75386994
Pig chromosome chr1
Pig SNP position 164720442
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
Region18q22.3
Chromosome idchr18
Chromosome position75386994
Reported geneTSHZ1
Mapped geneTSHZ1 - LOC105372200
Upstream gene id10194
Downstream gene id105372200
SNP gene ids
Upstream gene distance97044
Downstream gene distance19953
SNP risk allelers10514168-C
SNPsrs10514168
Merged0
SNP id current10514168
Contextupstream_gene_variant
Intergenic1
Allele frequency0.854
P value0.000000003
Pvalue mlog8.52287874528033
P value text
Or beta0.047
%95 Ci[0.031-0.062] unit decrease
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759