"Fulgent Genetics, Fulgent Genetics"[submitter] AND "RUNX1-AS1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 642956	NM_001754.5(RUNX1):c.508+2T>C	RUNX1, RUNX1-AS1	Single nucleotide variant (splice donor variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GPathogenic FDA Recognized database
Select item 566052	NM_001754.5(RUNX1):c.421T>G (p.Ser141Ala)	RUNX1, RUNX1-AS1 (S141A +1 more)	Single nucleotide variant (missense variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database