"ClinGen Myeloid Malignancy Variant Curation Expert Panel"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 996306	NC_000021.9:g.(?_35048832)_(35049298_?)del	LOC130066607, RUNX1	Deletion	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely pathogenic FDA Recognized database
Select item 1292686	NM_001754.5(RUNX1):c.-59-76A>G	LOC130066607, RUNX1	Single nucleotide variant (intron variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database