Variants in gene DYRK1A 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001347721.2(DYRK1A):c.1213-2A>G	rs1601315812
NM_001347721.2(DYRK1A):c.545_548del (p.Lys182fs)	rs1064796367
NM_001347721.2(DYRK1A):c.638-9_638-5del
NM_001347721.2(DYRK1A):c.664C>T (p.Arg222Ter)	rs780441716
NM_001347721.2(DYRK1A):c.827A>G (p.His276Arg)	rs2148612918
NM_001347721.2(DYRK1A):c.924+4_924+7del	rs1555984461

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