List of variants reported as likely benign for peroxisome biogenesis disorder 2A (Zellweger) by Illumina Laboratory Services, Illumina

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001351132.2(PEX5):c.-17+188T>C	rs186539500	0.01324
NM_001351132.2(PEX5):c.1718+13A>G	rs116873137	0.01093
NM_001351132.2(PEX5):c.*20G>C	rs145760932	0.00512
NM_001351132.2(PEX5):c.*1097T>C	rs116107198	0.00489
NM_001351132.2(PEX5):c.*114C>T	rs187571620	0.00329
NM_001351132.2(PEX5):c.1053G>A (p.Leu351=)	rs61740909	0.00290
NM_001351132.2(PEX5):c.*462G>C	rs75145323	0.00089
NM_001351132.2(PEX5):c.-17+273G>T	rs117442311	0.00027
NM_001351132.2(PEX5):c.-17+151G>A	rs146875386

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