rs137853306, TPM2

N. diseases: 6
Disease: Paresis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Paresis
CUI: C0030552
Disease: Paresis
0.010 GeneticVariation BEFREE It remains unknown, however, whether the E41K beta-Tm mutation directly affects regulation of muscle contraction, contributing to the muscle weakness. 18420702 2008