DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606771
rs267606771
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0917713
Disease:
Becker Muscular Dystrophy
A 0.710 CausalMutation CLINVAR
dbSNP: rs104894787
rs104894787
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0917713
Disease:
Becker Muscular Dystrophy
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894787
rs104894787
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0013264
Disease:
Muscular Dystrophy, Duchenne
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894788
rs104894788
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C4016476
Disease:
DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE
T 0.700 CausalMutation CLINVAR
dbSNP: rs104894789
rs104894789
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0013264
Disease:
Muscular Dystrophy, Duchenne
A 0.700 CausalMutation CLINVAR
dbSNP: rs1057516028
rs1057516028
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0241005
Disease:
Creatine phosphokinase serum increased
A 0.700 CausalMutation CLINVAR
dbSNP: rs1057518207
rs1057518207
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0013264
Disease:
Muscular Dystrophy, Duchenne
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518692
rs1057518692
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0013264
Disease:
Muscular Dystrophy, Duchenne
G 0.700 CausalMutation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1855580
Disease:
Exercise-induced muscle fatigue
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1855578
Disease:
Exercise-induced muscle cramps
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1855579
Disease:
Exercise-induced muscle stiffness
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0349588
Disease:
Short stature
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1844806
Disease:
Weight less than 3rd percentile
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C4021526
Disease:
Exercise-induced rhabdomyolysis
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1850830
Disease:
Exercise-induced myalgia
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026848
Disease:
Myopathy
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518834
rs1057518834
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C4021726
Disease:
EMG: myopathic abnormalities
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518866
rs1057518866
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026848
Disease:
Myopathy
C 0.700 CausalMutation CLINVAR
dbSNP: rs1057518962
rs1057518962
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C4021726
Disease:
EMG: myopathic abnormalities
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518962
rs1057518962
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1854301
Disease:
Motor delay
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518962
rs1057518962
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0476403
Disease:
Electromyogram abnormal
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518962
rs1057518962
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1843057
Disease:
Calf muscle hypertrophy
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518962
rs1057518962
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0037763
Disease:
Spasm
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518962
rs1057518962
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0151786
Disease:
Muscle Weakness
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057524037
rs1057524037
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0013264
Disease:
Muscular Dystrophy, Duchenne
T 0.700 CausalMutation CLINVAR