List of variants in gene DMD reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.10789C>T (p.Leu3597=)	rs1800281	0.00486
NM_004006.3(DMD):c.1483-7C>G	rs112463388	0.00162
NM_004006.3(DMD):c.8571T>C (p.Thr2857=)	rs72466570	0.00153
NM_004006.3(DMD):c.7183G>A (p.Ala2395Thr)	rs72466590	0.00126
NM_004006.3(DMD):c.1513G>C (p.Val505Leu)	rs140340626	0.00113
NM_004006.3(DMD):c.7571G>A (p.Arg2524His)	rs151244052	0.00109
NM_004006.3(DMD):c.4233+2C>T	rs147474070	0.00066
NM_004006.3(DMD):c.2457A>C (p.Leu819=)	rs72468680	0.00046
NM_004006.3(DMD):c.2490C>T (p.Asn830=)	rs72468679	0.00040
NM_004006.3(DMD):c.1095A>C (p.Gln365His)	rs1800266	0.00035
NM_004006.3(DMD):c.5010G>T (p.Trp1670Cys)	rs727503828	0.00032
NM_004006.3(DMD):c.1252A>T (p.Thr418Ser)	rs201341211	0.00026
NM_004006.3(DMD):c.9225-5795G>A	rs138287985	0.00025
NM_004006.3(DMD):c.2386G>A (p.Val796Ile)	rs139726281	0.00023
NM_004006.3(DMD):c.7310-7A>G	rs373230021	0.00023
NM_004006.3(DMD):c.6571C>T (p.Arg2191Trp)	rs149322279	0.00020
NM_004006.3(DMD):c.9486G>A (p.Glu3162=)	rs370724251	0.00015
NM_004006.3(DMD):c.3816G>C (p.Leu1272Phe)	rs760733415	0.00014
NM_004006.3(DMD):c.7151C>A (p.Ser2384Tyr)	rs185706283	0.00014
NM_004006.3(DMD):c.8027+7A>T	rs72466580	0.00013
NM_004006.3(DMD):c.3432+10A>G	rs746260475	0.00010
NM_004006.3(DMD):c.3794G>C (p.Trp1265Ser)	rs200213555	0.00010
NM_004006.3(DMD):c.4877T>A (p.Val1626Glu)	rs72468634	0.00010
NM_004006.3(DMD):c.9093C>T (p.Val3031=)	rs72466563	0.00007
NM_004006.3(DMD):c.2163G>A (p.Arg721=)	rs2048850262	0.00001
NM_004006.3(DMD):c.23_35del	rs752332058
NM_004006.3(DMD):c.923C>T (p.Thr308Ile)	rs145064612

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