RS747547178 FUS

Health Risk Chr 16:31190965
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Associated Conditions
Inborn genetic diseases
Tremor
hereditary essential
4
Amyotrophic lateral sclerosis type 6
Inborn genetic diseases
Tremor
hereditary essential
4
Amyotrophic lateral sclerosis type 6
Other Variants in FUS
rs121909667 rs121909668 rs121909669 rs121909671 rs267606832 rs387906627 rs387906628 rs186547381 rs387907274 rs886041776
Ask Dr. Hemsworth about this variant