Variants in gene RUNX1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

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HGVS	dbSNP	gnomAD frequency
NC_000021.9:g.(?_34787801)_(34799462_?)del
NM_001754.5(RUNX1):c.351+1G>C	rs1060502579
NM_001754.5(RUNX1):c.467C>A (p.Ala156Glu)	rs267607026
NM_001754.5(RUNX1):c.497G>A (p.Arg166Gln)	rs1060499616
NM_001754.5(RUNX1):c.679G>T (p.Glu227Ter)	rs1555889984

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