List of variants in gene DMD reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.2472C>G (p.Asn824Lys)	rs778811645	0.00001
NM_004006.3(DMD):c.2366A>G (p.Glu789Gly)
NM_004006.3(DMD):c.464A>G (p.Asn155Ser)	rs2148806581
NM_004006.3(DMD):c.5260G>A (p.Glu1754Lys)
NM_004006.3(DMD):c.607G>C (p.Ala203Pro)
NM_004006.3(DMD):c.6696C>G (p.Asn2232Lys)	rs886043675
NM_004006.3(DMD):c.917A>C (p.Tyr306Ser)	rs2147581077

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