List of variants in gene DMD reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.-188C>T	rs886043394	0.00018
NM_004006.3(DMD):c.10594G>A (p.Glu3532Lys)	rs766716563	0.00005
NM_004006.3(DMD):c.6464G>A (p.Arg2155Gln)	rs892121336	0.00001
NM_004006.3(DMD):c.*1033TGAT[4]	rs71860126
NM_004006.3(DMD):c.*1033TGAT[6]	rs71860126
NM_004006.3(DMD):c.10843_10845del (p.Ser3615del)	rs751391426
NM_004006.3(DMD):c.5801A>T (p.Glu1934Val)	rs878854620
NM_004006.3(DMD):c.6505A>G (p.Ile2169Val)	rs2095370242

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