List of variants in gene DYRK1A reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001347721.2(DYRK1A):c.234C>T (p.Asp78=)	rs1049764	0.00041
NM_001347721.2(DYRK1A):c.1014C>T (p.Leu338=)	rs143646885	0.00021
NM_001347721.2(DYRK1A):c.1818T>C (p.His606=)	rs372827991	0.00009
NM_001347721.2(DYRK1A):c.1762G>A (p.Ala588Thr)	rs200808105	0.00006
NM_001347721.2(DYRK1A):c.1509G>A (p.Ser503=)	rs763907769	0.00004
NM_001347721.2(DYRK1A):c.450C>T (p.Tyr150=)	rs1049773	0.00004
NM_001347721.2(DYRK1A):c.1644+9G>A	rs750741834	0.00003
NM_001347721.2(DYRK1A):c.1178C>G (p.Thr393Ser)	rs777270510	0.00002
NM_001347721.2(DYRK1A):c.1971G>A (p.Ser657=)	rs755724183	0.00002
NM_001347721.2(DYRK1A):c.2083G>A (p.Val695Ile)	rs200597760	0.00002
NM_001347721.2(DYRK1A):c.1461C>T (p.Ser487=)	rs1333054024	0.00001
NM_001347721.2(DYRK1A):c.1464C>T (p.Pro488=)	rs541193560	0.00001
NM_001347721.2(DYRK1A):c.1644+18T>C	rs755097100	0.00001
NM_001347721.2(DYRK1A):c.11-16394C>T
NM_001347721.2(DYRK1A):c.1665T>C (p.Ala555=)	rs1569404928
NM_001347721.2(DYRK1A):c.511G>A (p.Val171Met)

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