List of variants in gene ABCD1 reported as likely pathogenic by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000033.4(ABCD1):c.854G>A (p.Arg285His)	rs782635828	0.00002
NM_000033.4(ABCD1):c.102del (p.Leu35fs)	rs2148388645
NM_000033.4(ABCD1):c.1508del (p.Leu503fs)	rs2522296982
NM_000033.4(ABCD1):c.22dup (p.Arg8fs)	rs2148388526
NM_000033.4(ABCD1):c.900+1G>C
NM_000033.4(ABCD1):c.931C>T (p.Gln311Ter)	rs941503814

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