RS387907098 TGM6

Health Risk Chr 20:2400435
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Spinocerebellar ataxia type 35
Spinocerebellar ataxia type 35
Other Variants in TGM6
rs387907097 rs372250159 rs793888526 rs144201778 rs375595045 rs368599004 rs202184911 rs202245813 rs201338900 rs762242728
Ask Dr. Hemsworth about this variant