List of variants in gene KLC2 reported as benign for complex 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_001318734.2(KLC2):c.942+27T>C	rs525698	0.97319
NM_001318734.2(KLC2):c.1086C>T (p.Asp362=)	rs1151539	0.40491
NM_001318734.2(KLC2):c.1444-24C>T	rs474005	0.40488

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