Human SNP ID | rs10514168 |
---|---|
Human chromosome | chr18 |
Human SNP position | 75386994 |
Pig chromosome | chr1 |
Pig SNP position | 164720442 |
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 | 18q22.3 |
Chromosome id | chr18 |
Chromosome position | 75386994 |
Reported gene | TSHZ1 |
Mapped gene | TSHZ1 - LOC105372200 |
Upstream gene id | 10194 |
Downstream gene id | 105372200 |
SNP gene ids | |
Upstream gene distance | 97044 |
Downstream gene distance | 19953 |
SNP risk allele | rs10514168-C |
SNPs | rs10514168 |
Merged | 0 |
SNP id current | 10514168 |
Context | upstream_gene_variant |
Intergenic | 1 |
Allele frequency | 0.854 |
P value | 0.000000003 |
Pvalue mlog | 8.52287874528033 |
P value text | |
Or beta | 0.047 |
%95 Ci | [0.031-0.062] 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 |