ClinVar Miner

List of variants reported as likely benign for Peroxisome biogenesis disorder 9B

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Total variants: 14
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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.216T>C (p.Asp72=) rs1582732837
NM_000288.4(PEX7):c.315A>G (p.Gln105=) rs767901695
NM_000288.4(PEX7):c.330C>T (p.His110=) rs199648976
NM_000288.4(PEX7):c.340-8G>A rs528317074
NM_000288.4(PEX7):c.377A>C (p.Gln126Pro) rs113268723
NM_000288.4(PEX7):c.640C>T (p.Leu214=) rs1582759870
NM_000288.4(PEX7):c.695G>A (p.Arg232Gln) rs191969418
NM_000288.4(PEX7):c.867T>C (p.Thr289=) rs936175997
NM_000288.4(PEX7):c.903+7G>T rs1227993935
NM_000288.4(PEX7):c.903+8A>G rs779919482

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