List of variants reported as uncertain significance for glycogen storage disease VI by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002863.5(PYGL):c.1145C>T (p.Pro382Leu)	rs143759519	0.00440
NM_002863.5(PYGL):c.*78G>A	rs190588867	0.00133
NM_002863.5(PYGL):c.1582G>A (p.Asp528Asn)	rs138461745	0.00027
NM_002863.5(PYGL):c.1828-9T>A	rs372338710	0.00027
NM_002863.5(PYGL):c.2540A>T (p.Asn847Ile)	rs147863207	0.00011
NM_002863.5(PYGL):c.1454A>G (p.Asn485Ser)	rs138888959	0.00001

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