rs78993751[Variant ID] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1385113	NM_000033.4(ABCD1):c.1823G>C (p.Gly608Ala)	ABCD1 (G608A)	Single nucleotide variant (missense variant)	Adrenoleukodystrophy	GLikely pathogenic
Select item 218423	NM_000033.4(ABCD1):c.1823G>A (p.Gly608Asp)	ABCD1 (G608D)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity