CELF2, CUGBP Elav-like family member 2, 10659

N. diseases: 58; N. variants: 22
Disease: Motion Sickness ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10752212
rs10752212
Entrez Id: 10659
Gene Symbol: CELF2
CELF2
CUI: C0026603
Disease:
Motion Sickness 		G 0.700 GeneticVariation GWASCAT Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. 25628336 2015