RS186547381 FUS

Health Risk Chr 16:31190398
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What This Variant Does
"CLNSIG=5
Associated Conditions
Tremor
hereditary essential
4
Amyotrophic lateral sclerosis type 6
Frontotemporal dementia
Inborn genetic diseases
FUS-related disorder
Amyotrophic lateral sclerosis
Tremor
hereditary essential
4
Amyotrophic lateral sclerosis type 6
Frontotemporal dementia
Inborn genetic diseases
FUS-related disorder
Other Variants in FUS
rs121909667 rs121909668 rs121909669 rs121909671 rs267606832 rs387906627 rs387906628 rs387907274 rs886041776 rs886041389
Ask Dr. Hemsworth about this variant