RS878853280 FRRS1L
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
37
Seizure
Chorea
Progressive encephalopathy
Developmental and epileptic encephalopathy
37
Seizure
Chorea
Progressive encephalopathy
Other Variants in FRRS1L