Variants in gene KCND3 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001378969.1(KCND3):c.1348C>T (p.Leu450Phe)	rs150401343	0.00006
NM_001378969.1(KCND3):c.1111G>A (p.Gly371Arg)	rs1057521793
NM_001378969.1(KCND3):c.1150G>A (p.Gly384Ser)	rs1664632655
NM_001378969.1(KCND3):c.1174G>A (p.Val392Ile)	rs786205867

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