C1832388[trait identifier] AND "GenomeConnect - Invitae Patient Insigh - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 858173	NM_001754.5(RUNX1):c.844G>A (p.Asp282Asn)	RUNX1 (D282N +1 more)	Single nucleotide variant (missense variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 464003	NM_001754.5(RUNX1):c.70G>A (p.Gly24Arg)	RUNX1 (G24R)	Single nucleotide variant (missense variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance FDA Recognized database

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