Human SNP ID | rs6946969 |
---|---|
Human chromosome | chr7 |
Human SNP position | 70746041 |
Pig chromosome | chr3 |
Pig SNP position | 14900376 |
PubMed ID | 25628336 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25628336 |
Study | Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. |
Disease/Trait | Motion sickness |
Initial sample | 80,494 European ancestry individuals |
Replication sample | NA |
Region | 7q11.22 |
Chromosome id | chr7 |
Chromosome position | 70746041 |
Reported gene | AUTS2 |
Mapped gene | LOC105375347, AUTS2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105375347, 26053 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6946969-G |
SNPs | rs6946969 |
Merged | 0 |
SNP id current | 6946969 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.658 |
P value | 0.000000002 |
Pvalue mlog | 8.69897000433601 |
P value text | |
Or beta | 0.033 |
%95 Ci | [0.022-0.043] unit increase |
Platform | Illumina [7428049] (imputed) |
CNV | N |
Mapped trait | motion sickness |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006928 |
Study accession | GCST002759 |