List of variants in gene DMD reported as uncertain significance by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.2117C>A (p.Pro706Gln)	rs781015830	0.00004
NM_004006.3(DMD):c.221T>C (p.Leu74Pro)
NM_004006.3(DMD):c.3488A>C (p.Gln1163Pro)
NM_004006.3(DMD):c.6865G>A (p.Asp2289Asn)

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