Human SNP ID | rs1858111 |
---|---|
Human chromosome | chr1 |
Human SNP position | 95624175 |
Pig chromosome | chr4 |
Pig SNP position | 133665161 |
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 | 1p21.3 |
Chromosome id | chr1 |
Chromosome position | 95624175 |
Reported gene | RWDD3 |
Mapped gene | LOC100996635 - LOC101928219 |
Upstream gene id | 100996635 |
Downstream gene id | 101928219 |
SNP gene ids | |
Upstream gene distance | 108711 |
Downstream gene distance | 1275 |
SNP risk allele | rs1858111-G |
SNPs | rs1858111 |
Merged | 0 |
SNP id current | 1858111 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.567 |
P value | 0.00000000000004 |
Pvalue mlog | 13.397940008672 |
P value text | |
Or beta | 0.039 |
%95 Ci | [0.029-0.05] 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 |