List of variants reported as uncertain significance for spinal muscular atrophy by Molecular Genetics, Royal Melbourne Hospital

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001122955.4(BSCL2):c.1033C>T (p.Arg345Trp)	rs767820877	0.00001
NM_001376.5(DYNC1H1):c.10970G>C (p.Gly3657Ala)	rs761427653	0.00001
NM_001003800.2(BICD2):c.2234C>T (p.Ser745Leu)

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