List of variants in gene MAG reported as uncertain significance for Hereditary spastic paraplegia

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_002361.4(MAG):c.452C>T (p.Ala151Val)	rs144553163	0.00387
NM_002361.4(MAG):c.1117A>C (p.Ser373Arg)	rs142375870	0.00022
NM_002361.4(MAG):c.1646C>T (p.Ser549Leu)	rs767886169	0.00001

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