List of variants reported as pathogenic for Amyotrophic lateral sclerosis type 5; Hereditary spastic paraplegia 11; Charcot-Marie-Tooth disease axonal type 2X by Fulgent Genetics, Fulgent Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_025137.4(SPG11):c.1085G>A (p.Trp362Ter)	rs140385286	0.00005
NM_025137.4(SPG11):c.733_734del (p.Met245fs)	rs312262720	0.00005
NM_025137.4(SPG11):c.1348dup (p.Ile450fs)	rs312262725	0.00004
NM_025137.4(SPG11):c.5623C>T (p.Gln1875Ter)	rs141848292	0.00002
NM_025137.4(SPG11):c.5986dup (p.Cys1996fs)	rs312262775	0.00001
NM_025137.4(SPG11):c.4462_4463del (p.Val1488fs)	rs587777921
NM_025137.4(SPG11):c.6737_6740del (p.Ile2246fs)	rs312262781
NM_025137.4(SPG11):c.6739_6742del (p.Glu2247fs)	rs312262782

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