RS879328855 GOSR2

Health Risk Chr 17:46923193
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Associated Conditions
Progressive myoclonic epilepsy
Inborn genetic diseases
Hearing loss
autosomal recessive
Progressive myoclonic epilepsy
Inborn genetic diseases
Hearing loss
autosomal recessive
Other Variants in GOSR2
rs387906881 rs573306680 rs777442803 rs138510884 rs137975476 rs863223401 rs141554661 rs886039603 rs200210055 rs747791818
Ask Dr. Hemsworth about this variant