List of variants reported as uncertain significance for spinal muscular atrophy by Care4Rare-SOLVE, CHEO

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_177924.5(ASAH1):c.456A>C (p.Lys152Asn)	rs200455852	0.00004
NM_177924.5(ASAH1):c.410A>G (p.Tyr137Cys)	rs371666412	0.00001

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