List of variants in gene SCP2 reported as uncertain significance for peroxisomal disease

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002979.5(SCP2):c.230A>G (p.Tyr77Cys)	rs138573524	0.00008
NM_002979.5(SCP2):c.572A>G (p.His191Arg)	rs372168791	0.00001
NM_002979.5(SCP2):c.886C>T (p.Pro296Ser)	rs1342599570

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