Human SNP ID | rs2360806 |
---|---|
Human chromosome | chr8 |
Human SNP position | 52213174 |
Pig chromosome | chr4 |
Pig SNP position | 85090194 |
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 | 8q11.23 |
Chromosome id | chr8 |
Chromosome position | 52213174 |
Reported gene | ST18 |
Mapped gene | ST18 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9705 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2360806-C |
SNPs | rs2360806 |
Merged | 0 |
SNP id current | 2360806 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.162 |
P value | 0.00000000007 |
Pvalue mlog | 10.1549019599857 |
P value text | |
Or beta | 0.047 |
%95 Ci | [0.033-0.061] 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 |