List of variants in gene DMD reported as uncertain significance by MGZ Medical Genetics Center

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.10033C>G (p.Arg3345Gly)	rs398123827
NM_004006.3(DMD):c.1687C>A (p.Arg563Ser)	rs145739725
NM_004006.3(DMD):c.266T>C (p.Val89Ala)	rs1557058441
NM_004006.3(DMD):c.3327T>A (p.Asn1109Lys)
NM_004006.3(DMD):c.336_337delinsTT (p.Trp112_Asn113delinsCysTyr)
NM_004006.3(DMD):c.8028-12G>A

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