RS606231134 SYNE1

Health Risk Chr 6:152321898
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive ataxia
Beauce type
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
SYNE1-related disorder
Arthrogryposis multiplex congenita 3
myogenic type
Autosomal recessive ataxia
Beauce type
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
SYNE1-related disorder
Arthrogryposis multiplex congenita 3
myogenic type
Other Variants in SYNE1
rs119103243 rs119103244 rs119103245 rs606231135 rs119103248 rs1586285494 rs267600861 rs267600862 rs180727534 rs376511242
Ask Dr. Hemsworth about this variant