List of variants in gene DMD reported as uncertain significance by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.10889G>A (p.Arg3630Gln)	rs1057522606	0.00002
NM_004006.3(DMD):c.2303G>A (p.Arg768Gln)	rs769377296	0.00001
NM_004006.3(DMD):c.8509G>A (p.Asp2837Asn)	rs965718917	0.00001
NM_004006.3(DMD):c.3607G>A (p.Ala1203Thr)	rs1569562950
NM_004006.3(DMD):c.4180G>T (p.Ala1394Ser)
NM_004006.3(DMD):c.4832T>A (p.Val1611Asp)	rs2147469937
NM_004006.3(DMD):c.5386C>A (p.Pro1796Thr)
NM_004006.3(DMD):c.5582T>C (p.Leu1861Pro)	rs2147030312
NM_004006.3(DMD):c.9338G>A (p.Arg3113Gln)	rs1556320083

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