List of variants reported as likely benign for spinal muscular atrophy by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_017411.4(SMN2):c.859G>C (p.Gly287Arg)	rs121909192	0.00208
NM_001003800.2(BICD2):c.1126A>G (p.Thr376Ala)	rs757885234	0.00002
NM_000052.7(ATP7A):c.2096T>A (p.Met699Lys)	rs2149095258

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