RS141554661 GOSR2

Health Risk Chr 17:46932200
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What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive myoclonic epilepsy type 6
Progressive myoclonic epilepsy
Inborn genetic diseases
Muscular dystrophy
congenital
with or without seizures
GOSR2-related disorder
Colon adenocarcinoma
Progressive myoclonic epilepsy type 6
Progressive myoclonic epilepsy
Inborn genetic diseases
Muscular dystrophy
congenital
with or without seizures
GOSR2-related disorder
Other Variants in GOSR2
rs387906881 rs573306680 rs777442803 rs138510884 rs137975476 rs863223401 rs886039603 rs200210055 rs747791818 rs201423456
Ask Dr. Hemsworth about this variant