List of variants reported as uncertain significance for amyotrophic lateral sclerosis type 11 by Illumina Laboratory Services, Illumina

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		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_014845.6(FIG4):c.-132A>G	rs548471516	0.00150
NM_014845.6(FIG4):c.-138T>C	rs550585093	0.00016
NM_014845.6(FIG4):c.-84A>G	rs764845399	0.00013
NM_014845.6(FIG4):c.205C>T (p.Arg69Cys)	rs540674198	0.00013
NM_014845.6(FIG4):c.1271+5A>G	rs374583399	0.00012
NM_014845.6(FIG4):c.-112G>A	rs757848529	0.00008
NM_014845.6(FIG4):c.1940A>G (p.Tyr647Cys)	rs150301327	0.00008
NM_014845.6(FIG4):c.2096G>A (p.Arg699His)	rs750091928	0.00007
NM_014845.6(FIG4):c.109C>T (p.Arg37Cys)	rs368625871	0.00005
NM_014845.6(FIG4):c.2096+3A>G	rs374223402	0.00005
NM_014845.6(FIG4):c.2200G>A (p.Glu734Lys)	rs372846619	0.00005
NM_014845.5(FIG4):c.-152C>A	rs1408966015	0.00003
NM_014845.6(FIG4):c.243A>G (p.Lys81=)	rs200257799	0.00003
NM_014845.6(FIG4):c.2547-11A>G	rs745613994	0.00003
NM_014845.6(FIG4):c.2567C>T (p.Ser856Leu)	rs200970494	0.00003
NM_014845.6(FIG4):c.1482C>T (p.Asn494=)	rs776928002	0.00002
NM_014845.6(FIG4):c.2547-4A>G	rs886060985	0.00002
NM_014845.6(FIG4):c.2690T>C (p.Met897Thr)	rs764958115	0.00002
NM_014845.6(FIG4):c.-124A>G	rs544958043	0.00001
NM_014845.6(FIG4):c.-134C>G	rs560811735	0.00001
NM_014845.6(FIG4):c.1793T>A (p.Phe598Tyr)	rs751399063	0.00001
NM_014845.6(FIG4):c.2222C>T (p.Thr741Met)	rs1274229885	0.00001
NM_014845.6(FIG4):c.2552C>T (p.Pro851Leu)	rs201375273	0.00001
NM_014845.6(FIG4):c.1272-10C>G	rs201293291
NM_014845.6(FIG4):c.1889+9C>T	rs1777643262
NM_014845.6(FIG4):c.235G>A (p.Gly79Arg)	rs886060982
NM_014845.6(FIG4):c.2460A>C (p.Arg820Ser)	rs886060984
NM_014845.6(FIG4):c.2546+5G>C	rs1060501401

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