rs200916654, DYSF

N. diseases: 4
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 GeneticVariation CLINVAR
Muscular Dystrophy
CUI: C0026850
Disease: Muscular Dystrophy
0.700 GeneticVariation CLINVAR
Difficulty standing
CUI: C0241237
Disease: Difficulty standing
0.700 GeneticVariation CLINVAR
Creatine phosphokinase serum increased
CUI: C0241005
Disease: Creatine phosphokinase serum increased
0.700 GeneticVariation CLINVAR