RS878853282 FRRS1L

Health Risk Chr 9:109141466
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
37
Progressive encephalopathy
Chorea
Seizure
Inborn genetic diseases
FRRS1L-related disorder
Developmental and epileptic encephalopathy
37
Progressive encephalopathy
Chorea
Seizure
Inborn genetic diseases
FRRS1L-related disorder
Other Variants in FRRS1L
rs878853280 rs878853281 rs878853283 rs148986846 rs933379958 rs1054228594 rs149005559 rs530413587 rs779716535 rs1564232243
Ask Dr. Hemsworth about this variant