RS746633090 FUS

Health Risk Chr 16:31185076
Upload your DNA to see your genotype for this variant.
Associated Conditions
Amyotrophic lateral sclerosis type 6
Tremor
hereditary essential
4
Inborn genetic diseases
FUS-related disorder
Amyotrophic lateral sclerosis type 6
Tremor
hereditary essential
4
Inborn genetic diseases
FUS-related disorder
Other Variants in FUS
rs121909667 rs121909668 rs121909669 rs121909671 rs267606832 rs387906627 rs387906628 rs186547381 rs387907274 rs886041776
Ask Dr. Hemsworth about this variant