Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908457
rs121908457
MYOT ; LOC101928005
0.010 GeneticVariation BEFREE Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype. 17698502

2008