List of variants in gene DMD reported as likely pathogenic by Eurofins NTD LLC (GA)

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.6614+3310G>T	rs797045526
NM_004006.3(DMD):c.8217+18052A>G	rs886042109
NM_004006.3(DMD):c.8548-2_8549dup	rs1556656895

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