List of variants reported as benign for Peroxisome biogenesis disorder, complementation group 7 by Invitae

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002617.4(PEX10):c.291A>G (p.Thr97=)	rs2494598	0.74152
NM_002617.4(PEX10):c.913-4G>A	rs11586985	0.08566
NM_002617.4(PEX10):c.279C>T (p.Gly93=)	rs1143016	0.05120
NM_002617.4(PEX10):c.820A>G (p.Thr274Ala)	rs34154371	0.01899
NM_002617.4(PEX10):c.843G>A (p.Arg281=)	rs35082957	0.00846
NM_002617.4(PEX10):c.685G>C (p.Val229Leu)	rs139345520	0.00686
NM_002617.4(PEX10):c.318G>A (p.Leu106=)	rs146452560	0.00649
NM_002617.4(PEX10):c.332T>C (p.Leu111Pro)	rs35426403	0.00554
NM_002617.4(PEX10):c.6C>G (p.Ala2=)	rs112471479	0.00523
NM_002617.4(PEX10):c.621C>G (p.Pro207=)	rs140107510	0.00350
NM_002617.4(PEX10):c.495C>T (p.Phe165=)	rs150344828	0.00145
NM_002617.4(PEX10):c.627G>A (p.Glu209=)	rs141430704	0.00043
NM_002617.4(PEX10):c.435G>A (p.Met145Ile)	rs368273118	0.00003
NM_002617.4(PEX10):c.864C>T (p.Cys288=)	rs762621687	0.00001
NM_002617.4(PEX10):c.777-12del
NM_002617.4(PEX10):c.913-17del

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