List of variants in gene DMD reported as benign by Fulgent Genetics, Fulgent Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.7476T>C (p.Val2492=)	rs142153424	0.00626
NM_004006.3(DMD):c.5984A>T (p.Tyr1995Phe)	rs147927593	0.00113
NM_004006.3(DMD):c.2261G>T (p.Gly754Val)	rs151242451	0.00098
NM_004006.3(DMD):c.5203C>T (p.Arg1735Cys)	rs147904018	0.00054
NM_004006.3(DMD):c.2381-3T>C	rs147931243	0.00048
NM_004006.3(DMD):c.8945G>A (p.Arg2982Gln)	rs750579766	0.00001

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