ClinVar Miner

List of variants reported as uncertain significance for Peroxisome biogenesis disorder type 3B by Neuberg Centre For Genomic Medicine, NCGM

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_000286.3(PEX12):c.106_107delinsAT (p.Ala36Ile)

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