{{Rsnum
|rsid=41305353
|Gene=DMD
|Chromosome=X
|position=31478314
|Orientation=plus
|GMAF=0.03869
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=DMD
}}{{omim
|id=300377
|rsnum=41305353
|variant=0061
}}

{{ClinVar
|rsid=41305353
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=31496431
|CHROM=X
|GMAF=0.0391802
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050060000000140516110100
|GENEINFO=DMD:1756
|GENE_NAME=DMD
|GENE_ID=1756
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.31496431T>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=431; 300377.0061
|CLNSIG=5
|CLNCUI=C0013264
|CLNDBN=Duchenne muscular dystrophy; AllHighlyPenetrant
|Disease=Duchenne muscular dystrophy; AllHighlyPenetrant
|CLNACC=RCV000012018.4; RCV000080810.1
|Tags=PM;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9613; 0.03869
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1119:C0013264:310200:98896:76670001; CN169374
|COMMON=1
}}

{{GET Evidence
|gene=DMD
|aa_change=Glu2910Val
|aa_change_short=E2910V
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs41305353
|overall_frequency_n=260
|overall_frequency_d=8759
|overall_frequency=0.0296838
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=5
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|in_omim=Y
|pph2_score=0.77
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=5
|autoscore=5
|webscore=N
|n_web_uneval=5
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}