List of variants reported as uncertain significance for peroxisomal disease by MGZ Medical Genetics Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000318.3(PEX2):c.869T>G (p.Leu290Arg)	rs756496949	0.00001
NM_000033.4(ABCD1):c.664G>A (p.Val222Met)
NM_000033.4(ABCD1):c.700C>T (p.Arg234Cys)	rs1557052478
NM_014324.6(AMACR):c.149A>G (p.Lys50Arg)

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