ClinVar Miner

List of variants in gene RTN2 reported as likely benign for Spastic paraplegia, autosomal dominant

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Total variants: 4
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HGVS dbSNP
NM_005619.5(RTN2):c.1143G>A (p.Ala381=) rs45532933
NM_005619.5(RTN2):c.1168G>A (p.Gly390Ser) rs143937661
NM_005619.5(RTN2):c.1593C>T (p.Ala531=) rs148630935
NM_206900.2(RTN2):c.1162-12delC rs537146226

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