List of variants in gene DMD reported as uncertain significance for Primary familial dilated cardiomyopathy

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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.23_35del	rs752332058
NM_004006.3(DMD):c.4082G>A (p.Arg1361Lys)	rs753639717
NM_004006.3(DMD):c.4428G>T (p.Met1476Ile)	rs745757372
NM_004006.3(DMD):c.7712G>A (p.Arg2571Gln)	rs371588290
NM_004006.3(DMD):c.9352G>T (p.Ala3118Ser)	rs200928985

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