List of variants in gene DMD reported as benign by Athena Diagnostics Inc

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: 46

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.2645= (p.Asp882=)	rs228406	0.99999
NM_004006.3(DMD):c.7096= (p.Lys2366=)	rs1800275	0.78847
NM_004006.3(DMD):c.5234G>A (p.Arg1745His)	rs1801187	0.36912
NM_004006.3(DMD):c.7728T>C (p.Asn2576=)	rs1801188	0.15883
NM_004006.3(DMD):c.837G>A (p.Thr279=)	rs1800265	0.12849
NM_004006.3(DMD):c.1635A>G (p.Arg545=)	rs5927083	0.12751
NM_004006.3(DMD):c.8810= (p.Arg2937=)	rs1800280	0.04757
NM_004006.3(DMD):c.8734A>G (p.Asn2912Asp)	rs1800278	0.02976
NM_004006.3(DMD):c.8729A>T (p.Glu2910Val)	rs41305353	0.02876
NM_004006.3(DMD):c.6463C>T (p.Arg2155Trp)	rs1800273	0.02767
NM_004006.3(DMD):c.4162T>G (p.Phe1388Val)	rs28715870	0.02748
NM_004006.3(DMD):c.-8T>A	rs113726961	0.02450
NM_004006.3(DMD):c.4878G>T (p.Val1626=)	rs61733574	0.02120
NM_004006.3(DMD):c.5016T>A (p.Asn1672Lys)	rs16990264	0.02084
NM_004006.3(DMD):c.5724T>C (p.Asp1908=)	rs143159113	0.01630
NM_004006.3(DMD):c.3705C>T (p.Ala1235=)	rs143628111	0.01510
NM_004006.3(DMD):c.1554T>A (p.Asp518Glu)	rs61733587	0.01098
NM_004006.3(DMD):c.1225A>T (p.Thr409Ser)	rs34155804	0.01079
NM_004006.3(DMD):c.1997C>T (p.Ser666Leu)	rs34563188	0.00460
NM_004006.3(DMD):c.1718C>T (p.Ala573Val)	rs5972599	0.00436
NM_004006.3(DMD):c.3406A>T (p.Thr1136Ser)	rs3827462	0.00356
NM_004006.3(DMD):c.5182C>T (p.Arg1728Cys)	rs34102501	0.00327
NM_004006.3(DMD):c.802T>C (p.Leu268=)	rs1800264	0.00307
NM_004006.3(DMD):c.3970C>T (p.Arg1324Cys)	rs143184877	0.00208
NM_004006.3(DMD):c.2971G>C (p.Glu991Gln)	rs72468667	0.00146
NM_004006.3(DMD):c.7472A>G (p.Gln2491Arg)	rs147694734	0.00143
NM_004006.3(DMD):c.7183G>A (p.Ala2395Thr)	rs72466590	0.00126
NM_004006.3(DMD):c.5265C>T (p.Pro1755=)	rs145515413	0.00124
NM_004006.3(DMD):c.5984A>T (p.Tyr1995Phe)	rs147927593	0.00113
NM_004006.3(DMD):c.10262+1G>A	rs145603325	0.00069
NM_004006.3(DMD):c.4233+2C>T	rs147474070	0.00066
NM_004006.3(DMD):c.2199C>T (p.Ser733=)	rs149882431	0.00064
NM_004006.3(DMD):c.1028G>A (p.Arg343His)	rs61733589	0.00062
NM_004006.3(DMD):c.9165G>A (p.Thr3055=)	rs137905486	0.00024
NM_004006.3(DMD):c.1666G>A (p.Asp556Asn)	rs182708940	0.00020
NM_004006.3(DMD):c.1809G>A (p.Leu603=)	rs192176661	0.00020
NM_004006.3(DMD):c.6571C>T (p.Arg2191Trp)	rs149322279	0.00020
NM_004006.3(DMD):c.4072-3T>C	rs751657094	0.00019
NM_004006.3(DMD):c.2096C>G (p.Ala699Gly)	rs202008454	0.00018
NM_004006.3(DMD):c.5485C>G (p.Gln1829Glu)	rs754765424	0.00018
NM_004006.3(DMD):c.1503A>G (p.Glu501=)	rs770464589	0.00004
NM_004006.3(DMD):c.7397T>C (p.Met2466Thr)	rs764330616	0.00001
NM_004006.3(DMD):c.832-3C>T	rs777492476	0.00001
NM_004006.3(DMD):c.1869C>T (p.Leu623=)	rs1800267
NM_004006.3(DMD):c.932A>G (p.Asp311Gly)	rs760932600
NM_004006.3(DMD):c.94-9dup	rs3834997

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