ClinVar Miner

List of variants in gene RTN2 reported as uncertain significance for Spastic paraplegia, autosomal dominant

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Total variants: 7
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HGVS dbSNP
NM_005619.5(RTN2):c.*148G>A rs886054503
NM_005619.5(RTN2):c.*217G>A rs886054502
NM_005619.5(RTN2):c.*270C>T rs527298509
NM_005619.5(RTN2):c.*300G>C rs532093070
NM_005619.5(RTN2):c.*344C>T rs375889892
NM_005619.5(RTN2):c.*51T>C rs569611116
NM_005619.5(RTN2):c.986G>A (p.Ser329Asn) rs145653668

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