Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606771
rs267606771
DMD
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		A 0.710 CausalMutation CLINVAR

dbSNP: rs886044916
rs886044916
DMD
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs886044455
rs886044455
DMD
CUI: C3668940
Disease: Dmd-Associated Dilated Cardiomyopathy
Dmd-Associated Dilated Cardiomyopathy 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886043989
rs886043989
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886043676
rs886043676
DMD
CUI: C1854301
Disease: Motor delay
Motor delay 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886043676
rs886043676
DMD
CUI: C1866010
Disease: Proximal muscle weakness in lower limbs
Proximal muscle weakness in lower limbs 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886043676
rs886043676
DMD
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886043375
rs886043375
DMD
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		AG 0.700 CausalMutation CLINVAR

dbSNP: rs886043375
rs886043375
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		AG 0.700 CausalMutation CLINVAR

dbSNP: rs886043041
rs886043041
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886042840
rs886042840
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886042840
rs886042840
DMD
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886042747
rs886042747
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886042604
rs886042604
DMD
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		G 0.700 CausalMutation CLINVAR

dbSNP: rs886042604
rs886042604
DMD
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		G 0.700 CausalMutation CLINVAR

dbSNP: rs886042604
rs886042604
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886041344
rs886041344
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886039785
rs886039785
DMD
CUI: C0850703
Disease: Frequent falls
Frequent falls 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs886039785
rs886039785
DMD
CUI: C0234182
Disease: Gowers sign
Gowers sign 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs886039785
rs886039785
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs886039785
rs886039785
DMD
CUI: C1836296
Disease: Muscle Weakness Lower Limb
Muscle Weakness Lower Limb 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs886039785
rs886039785
DMD
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs886039785
rs886039785
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs886039785
rs886039785
DMD
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs878854621
rs878854621
DMD
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		C 0.700 CausalMutation CLINVAR