Variants in gene KMT2C 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_170606.3(KMT2C):c.1690A>T (p.Lys564Ter)	rs1554580083
NM_170606.3(KMT2C):c.4441C>T (p.Arg1481Ter)	rs587777073
NM_170606.3(KMT2C):c.7550C>G (p.Ser2517Ter)	rs779659766
NM_170606.3(KMT2C):c.8390dup (p.Glu2798fs)	rs747256476

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