rs1553521119, DYSF

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
CUI: C1850889
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
0.700 CausalMutation CLINVAR
Difficulty standing
CUI: C0241237
Disease: Difficulty standing
0.700 CausalMutation CLINVAR
Creatine phosphokinase serum increased
CUI: C0241005
Disease: Creatine phosphokinase serum increased
0.700 CausalMutation CLINVAR
Difficulty walking
CUI: C0311394
Disease: Difficulty walking
0.700 CausalMutation CLINVAR
Muscular Dystrophy
CUI: C0026850
Disease: Muscular Dystrophy
0.700 CausalMutation CLINVAR