Human SNP ID | rs11713169 |
---|---|
Human chromosome | chr3 |
Human SNP position | 173666799 |
Pig chromosome | chr13 |
Pig SNP position | 120871308 |
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 | 3q26.31 |
Chromosome id | chr3 |
Chromosome position | 173666799 |
Reported gene | NLGN1 |
Mapped gene | NLGN1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 22871 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11713169-C |
SNPs | rs11713169 |
Merged | 0 |
SNP id current | 11713169 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.16 |
P value | 0.0000000000006 |
Pvalue mlog | 12.2218487496163 |
P value text | |
Or beta | 0.052 |
%95 Ci | [0.038-0.067] 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 |