ClinVar Miner

List of variants reported as uncertain significance for Peroxisome biogenesis disorder 4A (Zellweger) by Myelin Disorders Clinic-Children's Medical Center/Medical Genetics Lab-Tarbiat Modares University, Children's Medical Center, Pediatrics Center of Excellence,

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000287.4(PEX6):c.231C>A (p.Ser77Arg) rs1770437263

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