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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001243177.4(ALDOA):c.1201G>A (p.Gly401Ser)	rs138824667	0.00256
NM_001243177.4(ALDOA):c.648C>G (p.Leu216=)	rs112110009	0.00124
NM_001243177.4(ALDOA):c.684T>C (p.Tyr228=)	rs1596813728
NM_001243177.4(ALDOA):c.966C>T (p.Ile322=)
NM_001365304.2(LOC112694756):c.*1509-16C>T

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