ClinVar Miner

List of variants reported as uncertain significance for Peroxisome biogenesis disorder 4B by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000287.4(PEX6):c.1183G>A (p.Gly395Arg)	rs755139673	0.00001
NM_000287.4(PEX6):c.2125G>A (p.Gly709Arg)	rs1254717257
NM_000287.4(PEX6):c.2273C>A (p.Ala758Asp)	rs2481207729

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