Variants with conflicting interpretations "likely pathogenic" from ClinGen Myeloid Malignancy Variant Curation Expert Panel and "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: 3

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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

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