List of variants reported as benign for Peroxisome biogenesis disorder 11A (Zellweger) by Illumina Laboratory Services, Illumina

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_002618.4(PEX13):c.*358G>A	rs1177230	0.98833
NM_002618.4(PEX13):c.*2147A>G	rs2564097	0.66023
NM_002618.4(PEX13):c.*952C>T	rs56739127	0.29127
NM_002618.4(PEX13):c.*1194G>A	rs75205376	0.13689
NM_002618.4(PEX13):c.1078C>G (p.Leu360Val)	rs74350038	0.02423
NM_002618.4(PEX13):c.*775G>A	rs143032208	0.02272
NM_002618.4(PEX13):c.*1652G>A	rs72877535	0.01126
NM_002618.4(PEX13):c.*1943G>A	rs183689971	0.00973
NM_002618.4(PEX13):c.674A>G (p.Asp225Gly)	rs116059308	0.00690

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