RS773955314 PNPLA6

Health Risk Chr 19:7557242
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary spastic paraplegia 39
Ataxia-hypogonadism-choroidal dystrophy syndrome
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
Laurence-Moon syndrome
Hereditary spastic paraplegia 39
Hereditary spastic paraplegia 39
Ataxia-hypogonadism-choroidal dystrophy syndrome
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
Laurence-Moon syndrome
Hereditary spastic paraplegia 39
Other Variants in PNPLA6
rs121434415 rs121434416 rs606231167 rs587777181 rs606231249 rs587777182 rs587777183 rs587777185 rs587777615 rs587777853
Ask Dr. Hemsworth about this variant