Disease: Motion Sickness ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs997295
rs997295
Entrez Id: 5607;107984718
Gene Symbol: MAP2K5;LOC107984718
MAP2K5;LOC107984718
CUI: C0026603
Disease:
Motion Sickness 		T 0.700 GeneticVariation GWASCAT Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. 25628336 2015