ClinVar Miner

List of variants reported as likely benign for Peroxisome biogenesis disorder 9B by Illumina Clinical Services Laboratory,Illumina

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP
NM_000288.4(PEX7):c.*115A>G	rs0
NM_000288.4(PEX7):c.*272A>G	rs186705952
NM_000288.4(PEX7):c.*38G>A	rs41288965
NM_000288.4(PEX7):c.-31G>A	rs115866467
NM_000288.4(PEX7):c.377A>C (p.Gln126Pro)	rs113268723

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