List of variants reported as likely benign for Hereditary spastic paraplegia 61

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_015161.3(ARL6IP1):c.494-9T>A	rs187822079	0.00110
NM_015161.3(ARL6IP1):c.494-18G>T	rs372011897	0.00058
NM_015161.3(ARL6IP1):c.430T>C (p.Ser144Pro)	rs201216108	0.00011
NM_015161.3(ARL6IP1):c.494-17T>G	rs540627798	0.00008
NM_015161.3(ARL6IP1):c.291-18G>A	rs558160589	0.00007
NM_015161.3(ARL6IP1):c.177C>T (p.Ile59=)	rs367581150	0.00005
NM_015161.3(ARL6IP1):c.36+19T>A	rs760294585	0.00004
NM_015161.3(ARL6IP1):c.489G>C (p.Leu163=)	rs543346989	0.00004
NM_015161.3(ARL6IP1):c.170+15A>G	rs748667940	0.00001
NM_015161.3(ARL6IP1):c.207C>T (p.Gly69=)	rs748647898	0.00001
NM_015161.3(ARL6IP1):c.36+20C>T	rs752378535	0.00001
NM_015161.3(ARL6IP1):c.42A>G (p.Ala14=)	rs755549983	0.00001
NM_015161.3(ARL6IP1):c.435T>G (p.Leu145=)	rs2030175530	0.00001
NM_015161.3(ARL6IP1):c.555A>G (p.Gly185=)	rs1320854180	0.00001
NM_015161.3(ARL6IP1):c.6G>A (p.Ala2=)	rs1341666694	0.00001
NM_015161.3(ARL6IP1):c.168T>C (p.Phe56=)
NM_015161.3(ARL6IP1):c.171-9T>A	rs372076598
NM_015161.3(ARL6IP1):c.306G>A (p.Gln102=)	rs201647214
NM_015161.3(ARL6IP1):c.345T>C (p.Thr115=)	rs758452451
NM_015161.3(ARL6IP1):c.36+11G>C	rs754374703
NM_015161.3(ARL6IP1):c.36+13dup	rs2141875992
NM_015161.3(ARL6IP1):c.37-20T>G	rs1219663998
NM_015161.3(ARL6IP1):c.390G>A (p.Lys130=)	rs2506661239
NM_015161.3(ARL6IP1):c.408+12G>A	rs1264921923
NM_015161.3(ARL6IP1):c.494-14T>C	rs2506652056
NM_015161.3(ARL6IP1):c.494-17dup	rs748985230
NM_015161.3(ARL6IP1):c.505C>T (p.Leu169=)	rs776403014
NM_015161.3(ARL6IP1):c.510G>A (p.Leu170=)	rs866131390

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