ClinVar Miner

List of variants in gene ABCD1 reported as likely pathogenic for not provided

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Total variants: 19
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NM_000033.3(ABCD1):c.1082-1G>A rs1557054153
NM_000033.3(ABCD1):c.1166G>A (p.Arg389His) rs886044777
NM_000033.3(ABCD1):c.1201C>G (p.Arg401Gly) rs727503786
NM_000033.3(ABCD1):c.1252C>T (p.Arg418Trp) rs128624220
NM_000033.3(ABCD1):c.1586G>A (p.Gly529Asp) rs398123103
NM_000033.3(ABCD1):c.1660C>A (p.Arg554Ser) rs398123104
NM_000033.3(ABCD1):c.1771C>T (p.Arg591Trp) rs398123106
NM_000033.3(ABCD1):c.1900G>A (p.Ala634Thr) rs782041940
NM_000033.3(ABCD1):c.2037G>A (p.Trp679Ter) rs1557055406
NM_000033.3(ABCD1):c.488G>A (p.Arg163His) rs1057517954
NM_000033.3(ABCD1):c.565C>T (p.Arg189Trp) rs1131691916
NM_000033.3(ABCD1):c.614C>A (p.Ala205Glu) rs398123113
NM_000033.3(ABCD1):c.761C>T (p.Thr254Met) rs1131691743
NM_000033.3(ABCD1):c.823C>T (p.Arg275Trp) rs782083931
NM_000033.3(ABCD1):c.874_876delGAG (p.Glu292del) rs387906496
NM_000033.3(ABCD1):c.880G>A (p.Ala294Thr) rs1131691954
NM_000033.3(ABCD1):c.886T>C (p.Tyr296His) rs797044611
NM_000033.3(ABCD1):c.887A>C (p.Tyr296Ser) rs797044610
NM_000033.4(ABCD1):c.662A>C (p.Asp221Ala)

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