Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518834
rs1057518834
DMD
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1568523935
rs1568523935
SLC25A42
G 0.700 GeneticVariation CLINVAR

dbSNP: rs398123383
rs398123383
LAMA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs267606640
rs267606640
AGL
0.010 GeneticVariation BEFREE Even heterozygous p.W1327X mutation carriers may present with mild non-progressive neuromuscular symptoms, such as exercise-induced myalgia and fatigue. 18924225

2008