List of variants reported as benign for hereditary spastic paraplegia by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_024306.5(FA2H):c.879C>T (p.Pro293=)	rs2301865	0.77852
NM_007347.5(AP4E1):c.222+18G>A	rs1147129	0.56600
NM_003119.4(SPG7):c.618+12T>C	rs3803679	0.45572
NM_007347.5(AP4E1):c.487T>C (p.Cys163Arg)	rs2306331	0.43394
NM_024306.5(FA2H):c.229C>T (p.Leu77=)	rs929881	0.33281
NM_007347.5(AP4E1):c.3387G>A (p.Gln1129=)	rs3825798	0.19899
NM_024306.5(FA2H):c.888A>G (p.Val296=)	rs11554621	0.15840
NM_015346.4(ZFYVE26):c.3118T>A (p.Ser1040Thr)	rs112787369	0.03993
NM_001166114.2(PNPLA6):c.3954C>T (p.Ala1318=)	rs34030828	0.00408
NM_003119.4(SPG7):c.987+5A>G	rs4785691

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