List of variants in gene PEX7 reported as likely benign for Peroxisome biogenesis disorder 9B

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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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.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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