RS587777854 PNPLA6
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Ataxia-hypogonadism-choroidal dystrophy syndrome
Hereditary spastic paraplegia 39
Ataxia-hypogonadism-choroidal dystrophy syndrome
Hereditary spastic paraplegia 39
Other Variants in PNPLA6