Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894127
rs104894127
TPM2
0.010 GeneticVariation BEFREE This may be the reason for both high Ca<sup>2+</sup>-sensitivity and contractures associated with the Arg91Gly mutation. 29097206

2017