List of variants in gene DMD studied for Primary dilated cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.2391T>G (p.Asn797Lys)	rs72468681	0.00714
NM_004006.3(DMD):c.3406A>T (p.Thr1136Ser)	rs3827462	0.00356
NM_004006.3(DMD):c.9682T>C (p.Phe3228Leu)	rs141392048	0.00180
NM_004006.3(DMD):c.7571G>A (p.Arg2524His)	rs151244052	0.00109
NM_004006.3(DMD):c.1337A>G (p.His446Arg)	rs72468699	0.00023
NM_004006.3(DMD):c.5701G>A (p.Ala1901Thr)	rs201302282	0.00016
NM_004006.3(DMD):c.7919C>G (p.Ala2640Gly)	rs146020545	0.00008
NM_004006.3(DMD):c.10228G>A (p.Val3410Ile)	rs751030250	0.00005
NM_004006.3(DMD):c.2245A>G (p.Ile749Val)	rs771803281	0.00005
NM_004006.3(DMD):c.2251C>T (p.Arg751Trp)	rs373475448	0.00004
NM_004006.3(DMD):c.*39A>T	rs371730838	0.00001
NM_004006.3(DMD):c.2972A>G (p.Glu991Gly)	rs747374618	0.00001
NM_004006.3(DMD):c.4449G>A (p.Met1483Ile)	rs765355046	0.00001
NM_004006.3(DMD):c.10034G>A (p.Arg3345Gln)
NM_004006.3(DMD):c.6118-3C>A	rs730880074

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