ClinVar Miner

List of variants reported as uncertain significance for Hereditary spastic paraplegia 7 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003119.4(SPG7):c.1238T>A (p.Val413Glu)	rs1244749062
NM_003119.4(SPG7):c.1249C>T (p.Arg417Cys)
NM_003119.4(SPG7):c.164C>A (p.Ala55Asp)	rs2057963306

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