List of variants reported as uncertain significance for peroxisomal disease by Mendelics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_014324.6(AMACR):c.857del (p.Ile286fs)	rs772921347	0.00004
NM_000033.4(ABCD1):c.199A>G (p.Met67Val)	rs1057114018	0.00002
NM_012062.5(DNM1L):c.1822A>C (p.Lys608Gln)	rs1592688400
NM_012062.5(DNM1L):c.1915C>T (p.Arg639Trp)	rs1011225865
NM_014324.6(AMACR):c.206T>C (p.Leu69Pro)	rs915168123

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