List of variants in gene DMD reported as not provided

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.7310-36C>T	rs72466586	0.01045
NM_004006.3(DMD):c.7183G>A (p.Ala2395Thr)	rs72466590	0.00126
NM_004006.3(DMD):c.9580A>C (p.Ile3194Leu)	rs181517869	0.00007
NM_004006.3(DMD):c.3889G>T (p.Gly1297Cys)	rs941573844	0.00003
NM_004006.3(DMD):c.4376G>A (p.Arg1459Gln)	rs755835144	0.00001
GRCh37/hg19 Xp21.1(chrX:32173956-32431534)x0
GRCh37/hg19 Xp21.1(chrX:32232129-32536506)x1
GRCh37/hg19 Xp21.1(chrX:33183494-33640512)x2
NM_004006.3(DMD):c.2273A>C (p.Asp758Ala)	rs750526692
NM_004006.3(DMD):c.5082G>A (p.Trp1694Ter)	rs1295394996
NM_004006.3(DMD):c.93+1G>T	rs886042604
NM_004006.3(DMD):c.93+5G>T
NM_004006.3(DMD):c.9749A>C (p.Glu3250Ala)	rs2148540881

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