List of variants in gene SCYL1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_020680.4(SCYL1):c.2200G>A (p.Asp734Asn)	rs202171988	0.00021
NM_020680.4(SCYL1):c.560C>T (p.Pro187Leu)	rs367912230	0.00005
NM_020680.4(SCYL1):c.1043AGA[1] (p.Lys349del)	rs562945480
NM_020680.4(SCYL1):c.767G>A (p.Arg256His)

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