List of variants in gene DMD reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.10249C>G (p.Pro3417Ala)	rs373898385	0.00008
NM_004006.3(DMD):c.5489G>T (p.Arg1830Ile)	rs369055628	0.00008
NM_004006.3(DMD):c.863G>C (p.Arg288Thr)	rs767304770	0.00007
NM_004006.3(DMD):c.4049G>A (p.Arg1350His)	rs750981128	0.00003
NM_004006.3(DMD):c.8890G>T (p.Gly2964Cys)	rs368114420	0.00002
NM_004006.3(DMD):c.1523A>G (p.Asn508Ser)	rs886044658	0.00001
NM_004006.3(DMD):c.2038A>G (p.Thr680Ala)	rs200504614	0.00001
NM_004006.3(DMD):c.3361C>T (p.Pro1121Ser)	rs150653420	0.00001
NM_004006.3(DMD):c.5419C>G (p.Leu1807Val)	rs1368648645	0.00001
NM_004006.3(DMD):c.6464G>A (p.Arg2155Gln)	rs892121336	0.00001
NM_004006.3(DMD):c.7016A>G (p.His2339Arg)	rs398124041	0.00001
NM_004006.3(DMD):c.31+4A>G	rs1557300092
NM_004006.3(DMD):c.3424T>C (p.Cys1142Arg)	rs772957337
NM_004006.3(DMD):c.881C>A (p.Pro294His)
NM_004006.3(DMD):c.9362-3C>T	rs752816247

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