List of variants reported as uncertain significance for HNSHA due to aldolase A deficiency by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001365304.2(LOC112694756):c.*621+4C>T	rs200278984	0.00204
NM_001243177.4(ALDOA):c.322G>A (p.Glu108Lys)	rs199852002	0.00001
NM_001243177.4(ALDOA):c.1141G>A (p.Glu381Lys)
NM_001243177.4(ALDOA):c.925A>G (p.Thr309Ala)

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