Variants with conflicting interpretations "pathogenic" from ClinGen Myeloid Malignancy Variant Curation Expert Panel and "likely pathogenic" from any submitter

Minimum review status of the submission from ClinGen Myeloid Malignancy Variant Curation Expert Panel:		Collection method of the submission from ClinGen Myeloid Malignancy Variant Curation Expert Panel:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.497G>A (p.Arg166Gln)	rs1060499616
NM_001754.5(RUNX1):c.679G>T (p.Glu227Ter)	rs1555889984

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