ClinVar Miner

List of variants in gene DMD reported as uncertain significance by Pars Genome Lab

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.-75G>A	rs778938887	0.00009
NM_004006.3(DMD):c.9352G>T (p.Ala3118Ser)	rs200928985

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