List of variants in gene RUNX1 reported as pathogenic for Thrombocytopenia

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: 4

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HGVS	dbSNP	gnomAD frequency
NC_000021.8:g.36284364_37074805del
NC_000021.9:g.34791392_34804065del
NM_001754.5(RUNX1):c.165dup (p.Leu56fs)	rs2058004321
NM_001754.5(RUNX1):c.351+1G>A	rs1060502579

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