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

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005619.4(RTN2):c.818_828del	rs1568624823
NM_005619.5(RTN2):c.148G>T (p.Glu50Ter)	rs1162797495
NM_005619.5(RTN2):c.170del (p.Gly57fs)	rs1968241252
NM_005619.5(RTN2):c.198C>A (p.Tyr66Ter)
NM_005619.5(RTN2):c.926del (p.Gly309fs)
NM_005619.5(RTN2):c.938dup (p.Thr314fs)	rs748397131

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