List of variants in gene SCYL1 reported as uncertain significance for Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_020680.4(SCYL1):c.804G>A (p.Met268Ile)	rs141670485	0.00076
NM_020680.4(SCYL1):c.1507T>C (p.Cys503Arg)	rs374754187	0.00016
NM_020680.4(SCYL1):c.2267G>C (p.Gly756Ala)	rs767319743

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