List of variants in gene DMD reported as uncertain significance by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.434G>A (p.Arg145Gln)	rs398123952	0.00005
NM_004006.3(DMD):c.10223C>T (p.Thr3408Ile)	rs777510517	0.00004
NM_004006.3(DMD):c.6068T>G (p.Leu2023Arg)	rs1060502662	0.00002
NM_004006.3(DMD):c.3937A>G (p.Met1313Val)	rs794729003	0.00001
NM_004006.3(DMD):c.5233C>T (p.Arg1745Cys)	rs1326450715	0.00001

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