"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 1180228	NM_001754.5(RUNX1):c.58+265G>A	LOC130066606, RUNX1	Single nucleotide variant (intron variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 1250489	NM_001754.5(RUNX1):c.58+264C>T	LOC130066606, RUNX1	Single nucleotide variant (intron variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database