RS387906881 GOSR2

Health Risk Chr 17:46935122
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What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive myoclonic epilepsy type 6
Muscular dystrophy
Progressive myoclonic epilepsy
congenital
with or without seizures
Inborn genetic diseases
Progressive myoclonic epilepsy type 6
Muscular dystrophy
Progressive myoclonic epilepsy
congenital
with or without seizures
Inborn genetic diseases
Other Variants in GOSR2
rs573306680 rs777442803 rs138510884 rs137975476 rs863223401 rs141554661 rs886039603 rs200210055 rs747791818 rs201423456
Ask Dr. Hemsworth about this variant