List of variants in gene DMD reported as uncertain significance by Klaassen Lab, Charite University Medicine Berlin

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_004006.3(DMD):c.5723A>T (p.Asp1908Val)	rs145266970	0.00014
NM_004006.3(DMD):c.8996C>T (p.Ala2999Val)	rs762577093	0.00001
NM_004006.3(DMD):c.2273A>C (p.Asp758Ala)	rs750526692

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