RS147484110 CSTB

Health Risk Chr 21:43774760
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What This Variant Does
"CLNSIG=5
Associated Conditions
Unverricht-Lundborg syndrome
Inborn genetic diseases
Progressive myoclonic epilepsy
Chorea
Dyskinesia
Encephalopathy
Microcephaly
Cerebral dysmyelination
Hepatocellular carcinoma
Unverricht-Lundborg syndrome
Inborn genetic diseases
Progressive myoclonic epilepsy
Chorea
Dyskinesia
Encephalopathy
Other Variants in CSTB
rs11553836 rs1057521317 rs1044894207 rs1555888363 rs779920568 rs1569006250 rs1601855887 rs1257171692 rs2517171405 rs763450239
Ask Dr. Hemsworth about this variant