{{Rsnum
|rsid=1801187
|Gene=DMD
|Chromosome=X
|position=32362879
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.448
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=DMD
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 33.8 | 21.5 | 44.6
| HCB | 62.2 | 20.0 | 17.8
| JPT | 38.6 | 29.5 | 31.8
| YRI | 0.0 | 0.7 | 99.3
| ASW | 5.5 | 5.5 | 89.1
| CHB | 62.2 | 20.0 | 17.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.9 | 0.9 | 98.1
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1801187
|allele=T
|frequency=0.433
|uid=1103673020208
|type=homozygous_SNP
|hugo=DMD
|ensembl gene=ENSG00000198947
|ensembl transcript=ENST00000357033
|sift=AFFECT FUNCTION
|disease=Defects in DMD are a cause of dilated cardiomyopathy (MIM:302045); also known as X-linked dilated cardiomyopathy (XLCM). Dystrophin mutations may predispose to common sporadic cardiomyopathy cases.
}}

{{GET Evidence
|gene=DMD
|aa_change=Arg1745His
|aa_change_short=R1745H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1801187
|overall_frequency_n=2947
|overall_frequency_d=8759
|overall_frequency=0.336454
|n_genomes=15
|n_genomes_annotated=0
|n_haplomes=27
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.999
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=1
|autoscore=3
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}