Variant: rs1554967681 

    present in Gene: SCYL1
    present in Chromosome: 11
    Position on Chromosome: 65525631
    Alleles of this Variant: C/T

rs1554967681 in SCYL1 gene and Liver Failure, Acute PMID 29419818 2018 SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN).

rs1554967681 in SCYL1 gene and Nerve Degeneration PMID 29419818 2018 SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN).