List of variants in gene RUNX1 reported as uncertain significance for Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1; Acute myeloid leukemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.-59-10C>T	rs578080277	0.00018
NM_001754.5(RUNX1):c.649G>A (p.Gly217Arg)	rs749004431	0.00006
NM_001754.5(RUNX1):c.1265A>C (p.Glu422Ala)	rs2056451758	0.00004
NM_001754.5(RUNX1):c.787C>T (p.Pro263Ser)	rs370315332	0.00003
NM_001754.5(RUNX1):c.421T>G (p.Ser141Ala)	rs1182543054	0.00001
NM_001754.5(RUNX1):c.764A>G (p.His255Arg)	rs746977462	0.00001
NM_001754.5(RUNX1):c.739C>T (p.Pro247Ser)	rs2057112093

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