List of variants in gene DMD reported as uncertain significance by AiLife Diagnostics, AiLife Diagnostics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.9716A>G (p.His3239Arg)	rs765865134	0.00005
NM_004006.3(DMD):c.1062G>C (p.Trp354Cys)	rs1569376447
NM_004006.3(DMD):c.1813-3C>T	rs181399181
NM_004006.3(DMD):c.4345-3C>G	rs2097987224
NM_004006.3(DMD):c.5279T>C (p.Leu1760Pro)	rs2097841814

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