List of variants reported as uncertain significance for spinal muscular atrophy by Institute of Human Genetics, Cologne University

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001365951.3(KIF1B):c.1771G>A (p.Gly591Arg)	rs145266399	0.00024
NM_003119.4(SPG7):c.233T>A (p.Leu78Ter)	rs121918358	0.00014
NM_006329.4(FBLN5):c.605G>T (p.Gly202Val)	rs137901671	0.00001
NM_015046.7(SETX):c.7711C>T (p.Pro2571Ser)	rs1554801479
NM_016955.4(SEPSECS):c.812G>T (p.Arg271Leu)	rs573577287

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