rs121912633, TRPV4

N. diseases: 10
Disease: Channelopathies ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Channelopathies
CUI: C1720983
Disease: Channelopathies
0.010 GeneticVariation BEFREE The human TRPV4(V620I) channelopathy mutation was transfected into primary porcine chondrocytes and caused significant (2.6-fold) up-regulation of follistatin (FST) expression levels. 24577120 2014