List of variants in gene DYRK1A reported as likely pathogenic by GenomeConnect - Simons Searchlight

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001347721.2(DYRK1A):c.1373G>A (p.Arg458Gln)	rs797045041
NM_001347721.2(DYRK1A):c.1378del (p.Gln460fs)	rs1555990958
NM_001347721.2(DYRK1A):c.924+4_924+7del	rs1555984461

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