List of variants reported as benign for Glycogen storage disease, type VI by Illumina Laboratory Services, Illumina

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_002863.5(PYGL):c.2016C>T (p.Thr672=)	rs15669	0.21064
NM_002863.4(PYGL):c.-127A>G	rs67490748	0.20002
NM_002863.5(PYGL):c.*7G>C	rs1042266	0.17763
NM_002863.5(PYGL):c.1020C>T (p.Asp340=)	rs2075643	0.16448
NM_002863.5(PYGL):c.664G>A (p.Val222Ile)	rs946616	0.09756
NM_002863.5(PYGL):c.153C>T (p.Asp51=)	rs77316189	0.07133
NM_002863.5(PYGL):c.93T>C (p.Ser31=)	rs17123244	0.04608
NM_002863.5(PYGL):c.1621-6T>C	rs74539788	0.01217
NM_002863.5(PYGL):c.2416A>T (p.Ile806Leu)	rs34313873	0.01205
NM_002863.5(PYGL):c.962G>A (p.Arg321His)	rs116465563	0.00878
NM_002863.5(PYGL):c.928C>T (p.Arg310Cys)	rs35501326	0.00753
NM_002863.5(PYGL):c.1093-6C>A	rs147211684	0.00613
NM_002863.5(PYGL):c.2112T>C (p.Ala704=)	rs35110875	0.00531
NM_002863.5(PYGL):c.176C>T (p.Thr59Met)	rs150483902	0.00507
NM_002863.5(PYGL):c.-29A>C	rs538311514	0.00001
NM_002863.5(PYGL):c.*11del	rs3216001
NM_002863.5(PYGL):c.1828-2del	rs11356035

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