RS535912271 SCYL1

Health Risk Chr 11:65526274
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Associated Conditions
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
SCYL1-related disorder
Inborn genetic diseases
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
SCYL1-related disorder
Inborn genetic diseases
Other Variants in SCYL1
rs141670485 rs143168314 rs201043872 rs201581270 rs1855366408 rs773812714 rs1320473430 rs2496024369 rs2495967037 rs1481969607
Ask Dr. Hemsworth about this variant