List of variants reported as likely benign for hereditary spastic paraplegia 31 by Illumina Laboratory Services, Illumina

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001371279.1(REEP1):c.*2457G>C	rs77055865	0.03118
NM_001371279.1(REEP1):c.*1415G>T	rs116705276	0.02275
NM_001371279.1(REEP1):c.*94T>C	rs141976852	0.02270
NM_001371279.1(REEP1):c.*2513G>A	rs115098584	0.02268
NM_001371279.1(REEP1):c.*2579T>C	rs11902617	0.02248
NM_001371279.1(REEP1):c.*954G>A	rs17510310	0.01856
NM_001371279.1(REEP1):c.*2995T>C	rs17438464	0.01493
NM_001371279.1(REEP1):c.*737T>C	rs150465452	0.01271
NM_001371279.1(REEP1):c.*2131G>A	rs58401741	0.01166
NM_001371279.1(REEP1):c.*965G>A	rs76860896	0.01007
NM_001371279.1(REEP1):c.*1325T>C	rs3731816	0.00394
NM_001371279.1(REEP1):c.*1614G>A	rs3731817	0.00389
NM_001371279.1(REEP1):c.*1217A>G	rs190070319	0.00083
NM_001371279.1(REEP1):c.844G>A (p.Glu282Lys)	rs189652973	0.00041

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