List of variants in gene RUNX1 reported as not provided for blood coagulation disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.155T>A (p.Met52Lys)	rs200431130	0.00028
NM_001754.5(RUNX1):c.70G>A (p.Gly24Arg)	rs1399187182
NM_001754.5(RUNX1):c.844G>A (p.Asp282Asn)	rs762953695

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