rs387906905, TRPV4

N. diseases: 10
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Gait abnormality
CUI: C0575081
Disease: Gait abnormality
0.700 GeneticVariation CLINVAR TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies. 21288981 2011