List of variants reported as uncertain significance for neuronopathy, distal hereditary motor, type 2C by Illumina Laboratory Services, Illumina

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006308.3(HSPB3):c.-89T>C	rs186550955	0.00064
NM_006308.3(HSPB3):c.-67C>T	rs913988211	0.00009
NM_006308.3(HSPB3):c.*10G>A	rs200960902	0.00007
NM_006308.3(HSPB3):c.*16T>G	rs201783790	0.00004
NM_006308.3(HSPB3):c.67C>T (p.Arg23Ter)	rs755999042	0.00003
NM_006308.3(HSPB3):c.*11G>T	rs1761047037
NM_006308.3(HSPB3):c.*79C>T	rs898535055
NM_006308.3(HSPB3):c.158C>A (p.Ser53Tyr)	rs756831768

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