Variants in gene ABCD1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_000033.4(ABCD1):c.707G>A (p.Arg236His)	rs201455322	0.00114
NM_000033.4(ABCD1):c.895C>T (p.His299Tyr)	rs202195978	0.00088
NM_000033.4(ABCD1):c.41C>G (p.Thr14Arg)	rs782161942	0.00047
NM_000033.4(ABCD1):c.1810G>A (p.Val604Ile)	rs151201945	0.00034
NM_000033.4(ABCD1):c.1780+4G>A	rs193922095	0.00014
NM_000033.4(ABCD1):c.1914C>T (p.Asp638=)	rs199723613	0.00007
NM_000033.4(ABCD1):c.392G>T (p.Gly131Val)	rs367799134	0.00005
NM_000033.4(ABCD1):c.1327G>A (p.Ala443Thr)	rs782647014	0.00002
NM_000033.4(ABCD1):c.1452C>G (p.Pro484=)	rs782546330	0.00001
NM_000033.4(ABCD1):c.1744G>A (p.Val582Ile)	rs76180859	0.00001
NM_000033.4(ABCD1):c.1092C>G (p.Ala364=)	rs782250326
NM_000033.4(ABCD1):c.1816T>C (p.Ser606Pro)	rs201774661
NM_000033.4(ABCD1):c.1823G>A (p.Gly608Asp)	rs78993751

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