Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863225005
rs863225005
DMD
A 0.700 CausalMutation CLINVAR Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort. 19937601

2009
dbSNP: rs863225005
rs863225005
DMD
A 0.700 CausalMutation CLINVAR Mutation rates in the dystrophin gene: a hotspot of mutation at a CpG dinucleotide. 15643612

2005