RS119103243 SYNE1

Health Risk Chr 6:152381320
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive ataxia
Beauce type
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Arthrogryposis multiplex congenita 3
myogenic type
Autosomal recessive ataxia
Beauce type
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Arthrogryposis multiplex congenita 3
myogenic type
Other Variants in SYNE1
rs606231134 rs119103244 rs119103245 rs606231135 rs119103248 rs1586285494 rs267600861 rs267600862 rs180727534 rs376511242
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