ClinVar Miner

List of variants reported as likely benign for X-linked cerebral adrenoleukodystrophy by Invitae

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_000033.4(ABCD1):c.1092C>T (p.Ala364=) rs782250326
NM_000033.4(ABCD1):c.1142G>A (p.Arg381His) rs782755297
NM_000033.4(ABCD1):c.1228A>T (p.Thr410Ser) rs782161850
NM_000033.4(ABCD1):c.1404G>A (p.Val468=) rs782072629
NM_000033.4(ABCD1):c.1455A>C (p.Ser485=) rs150878397
NM_000033.4(ABCD1):c.1467G>A (p.Val489=) rs782516659
NM_000033.4(ABCD1):c.1629G>A (p.Pro543=) rs782278443
NM_000033.4(ABCD1):c.1683C>T (p.Asp561=) rs199997983
NM_000033.4(ABCD1):c.1743C>T (p.Asp581=) rs782026057
NM_000033.4(ABCD1):c.1781-7C>T rs79915675
NM_000033.4(ABCD1):c.1960C>T (p.Leu654=) rs782809410
NM_000033.4(ABCD1):c.2043C>G (p.Phe681Leu) rs782327280
NM_000033.4(ABCD1):c.2076G>A (p.Leu692=) rs1557055415
NM_000033.4(ABCD1):c.2079G>A (p.Thr693=) rs781935761
NM_000033.4(ABCD1):c.2190G>A (p.Pro730=) rs193922096
NM_000033.4(ABCD1):c.38A>C (p.Asn13Thr) rs183021839
NM_000033.4(ABCD1):c.414C>T (p.Leu138=) rs782197275
NM_000033.4(ABCD1):c.54G>A (p.Thr18=) rs781855598
NM_000033.4(ABCD1):c.564G>C (p.Gly188=) rs1603232017
NM_000033.4(ABCD1):c.795C>T (p.Phe265=) rs782336092
NM_000033.4(ABCD1):c.819G>A (p.Ala273=) rs782165410

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