RS545986367 CSTB

Health Risk Chr 21:43774690
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What This Variant Does
"CLNSIG=5
Associated Conditions
Unverricht-Lundborg syndrome
Inborn genetic diseases
Progressive myoclonic epilepsy
Unverricht-Lundborg syndrome
Inborn genetic diseases
Progressive myoclonic epilepsy
Other Variants in CSTB
rs11553836 rs1057521317 rs1044894207 rs1555888363 rs779920568 rs1569006250 rs1601855887 rs1257171692 rs2517171405 rs763450239
Ask Dr. Hemsworth about this variant