List of variants in gene RTN2 reported as pathogenic for hereditary spastic paraplegia 12

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005619.5(RTN2):c.939del (p.Thr314fs)	rs768449676	0.00005
NM_005619.5(RTN2):c.1100C>T (p.Ser367Phe)	rs140494585	0.00001
NC_000019.10:g.(?_45485294_45497047_?)del
NM_005619.5(RTN2):c.103C>T (p.Arg35Ter)
NM_005619.5(RTN2):c.178dup (p.Arg60fs)	rs763387041

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