List of variants in gene DMD reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.5016T>A (p.Asn1672Lys)	rs16990264	0.02084
NM_004006.3(DMD):c.832-17C>A	rs72470514	0.01678
NM_004006.3(DMD):c.5724T>C (p.Asp1908=)	rs143159113	0.01630
NM_004006.3(DMD):c.1554T>A (p.Asp518Glu)	rs61733587	0.01098
NM_004006.3(DMD):c.6322C>T (p.Arg2108Cys)	rs16990169	0.00981
NM_004006.3(DMD):c.3603+8A>G	rs193249735	0.00743
NM_004006.3(DMD):c.10789C>T (p.Leu3597=)	rs1800281	0.00486
NM_004006.3(DMD):c.7542+13A>G	rs72466585	0.00407
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.1028G>A (p.Arg343His)	rs61733589	0.00062
NM_004006.3(DMD):c.3163-18T>C	rs72468662	0.00036
NM_004006.3(DMD):c.3379C>G (p.Leu1127Val)	rs141887693	0.00019
NM_004006.3(DMD):c.5048C>G (p.Thr1683Ser)	rs146420425	0.00010
NM_004006.3(DMD):c.6117+15C>T	rs754718247	0.00006
NM_004006.3(DMD):c.1713T>A (p.Phe571Leu)	rs587782936	0.00005
NM_004006.3(DMD):c.1742C>T (p.Ala581Val)	rs763155705	0.00004
NM_004006.3(DMD):c.1462C>T (p.Arg488Cys)	rs758932385	0.00003
NM_004006.3(DMD):c.6726A>G (p.Lys2242=)	rs145993057	0.00003
NM_004006.3(DMD):c.2842A>G (p.Met948Val)	rs186628781	0.00002
NM_004006.3(DMD):c.2381-7T>G	rs1201559737	0.00001
NM_004006.3(DMD):c.10554-29_10554-20del	rs200138464
NM_004006.3(DMD):c.11031A>G (p.Gly3677=)	rs2147665754
NM_004006.3(DMD):c.2328A>G (p.Lys776=)	rs1603634973
NM_004006.3(DMD):c.94-9dup	rs3834997

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