Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1557303544
rs1557303544
DMD
A 0.700 CausalMutation CLINVAR Diagnostic strategy for the detection of dystrophin gene mutations in asian patients and carriers using immortalized cell lines. 16566881

2006
dbSNP: rs1557303544
rs1557303544
DMD
A 0.700 CausalMutation CLINVAR Experience and strategy for the molecular testing of Duchenne muscular dystrophy. 16049303

2005