Human SNP ID | rs997295 |
---|---|
Human chromosome | chr15 |
Human SNP position | 67724005 |
Pig chromosome | chr1 |
Pig SNP position | 183472937 |
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 | 15q23 |
Chromosome id | chr15 |
Chromosome position | 67724005 |
Reported gene | MAP2K5 |
Mapped gene | MAP2K5 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 5607 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs997295-T |
SNPs | rs997295 |
Merged | 0 |
SNP id current | 997295 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.588 |
P value | 0.000000003 |
Pvalue mlog | 8.52287874528033 |
P value text | |
Or beta | 0.033 |
%95 Ci | [0.022-0.044] unit decrease |
Platform | Illumina [7428049] (imputed) |
CNV | N |
Mapped trait | motion sickness |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006928 |
Study accession | GCST002759 |