SNP Detail For rs11713169
1.Mapping Information
Human SNP ID rs11713169
Human chromosome chr3
Human SNP position 173666799
Pig chromosome chr13
Pig SNP position 120871308
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
Region3q26.31
Chromosome idchr3
Chromosome position173666799
Reported geneNLGN1
Mapped geneNLGN1
Upstream gene id
Downstream gene id
SNP gene ids22871
Upstream gene distance
Downstream gene distance
SNP risk allelers11713169-C
SNPsrs11713169
Merged0
SNP id current11713169
Contextintron_variant
Intergenic0
Allele frequency0.16
P value0.0000000000006
Pvalue mlog12.2218487496163
P value text
Or beta0.052
%95 Ci[0.038-0.067] unit decrease
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759