SNP Detail For rs61759167
1.Mapping Information
Human SNP ID rs61759167
Human chromosome chr1
Human SNP position 3175023
Pig chromosome chr6
Pig SNP position 59494991
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
Region1p36.32
Chromosome idchr1
Chromosome position3175023
Reported genePRDM16
Mapped genePRDM16
Upstream gene id
Downstream gene id
SNP gene ids63976
Upstream gene distance
Downstream gene distance
SNP risk allelers61759167-T
SNPsrs61759167
Merged0
SNP id current61759167
Contextintron_variant
Intergenic0
Allele frequency0.231
P value0.0000000000004
Pvalue mlog12.397940008672
P value text
Or beta0.047
%95 Ci[0.034-0.059] unit increase
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759