RS143900928 SYNE1
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Associated Conditions
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Autosomal recessive ataxia
Beauce type
Arthrogryposis multiplex congenita 3
myogenic type
Inborn genetic diseases
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Autosomal recessive ataxia
Beauce type
Arthrogryposis multiplex congenita 3
myogenic type
Inborn genetic diseases
Other Variants in SYNE1