"Fulgent Genetics, Fulgent Genetics"[submitter] AND "ABCB7"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 368658	NM_001271696.3(ABCB7):c.1032+12A>G	ABCB7	Single nucleotide variant (intron variant)	X-linked sideroblastic anemia with ataxia +3 more	GBenign/Likely benign
Select item 136242	NM_001271696.3(ABCB7):c.312C>T (p.Leu104=)	ABCB7	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign