rs1554967761, SCYL1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Liver Failure, Acute
CUI: C0162557
Disease: Liver Failure, Acute
0.700 CausalMutation CLINVAR SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN). 29419818 2018
Nerve Degeneration
CUI: C0027746
Disease: Nerve Degeneration
0.700 CausalMutation CLINVAR SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN). 29419818 2018