Variants in gene GATA2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 7

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HGVS	dbSNP	gnomAD frequency
NM_032638.5(GATA2):c.1081C>T (p.Arg361Cys)	rs1426175410	0.00001
NM_032638.5(GATA2):c.1017+572C>T	rs1559985787
NM_032638.5(GATA2):c.1045T>C (p.Cys349Arg)	rs1576745260
NM_032638.5(GATA2):c.1084C>T (p.Arg362Ter)	rs1553770510
NM_032638.5(GATA2):c.1113C>A (p.Asn371Lys)	rs376003468
NM_032638.5(GATA2):c.1117T>C (p.Cys373Arg)	rs387906633
NM_032638.5(GATA2):c.1186C>T (p.Arg396Trp)	rs1576744529

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