RS794727986 SYNE1

Health Risk Chr 6:152293990
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Autosomal recessive ataxia
Beauce type
SYNE1-related disorder
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Inborn genetic diseases
Autosomal recessive ataxia
Beauce type
SYNE1-related disorder
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Other Variants in SYNE1
rs606231134 rs119103243 rs119103244 rs119103245 rs606231135 rs119103248 rs1586285494 rs267600861 rs267600862 rs180727534
Ask Dr. Hemsworth about this variant