RS1554967681 SCYL1

Health Risk Chr 11:65525631
Upload your DNA to see your genotype for this variant.
Associated Conditions
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
Other Variants in SCYL1
rs141670485 rs143168314 rs201043872 rs201581270 rs1855366408 rs773812714 rs1320473430 rs2496024369 rs2495967037 rs1481969607
Ask Dr. Hemsworth about this variant