{{Rsnum
|rsid=228406
|Gene=DMD
|Chromosome=X
|position=32485077
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.2703
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DMD
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 54.0 | 21.2 | 24.8
| HCB | 84.7 | 10.9 | 4.4
| JPT | 72.3 | 14.3 | 13.4
| YRI | 57.8 | 22.4 | 19.7
| ASW | 52.6 | 26.3 | 21.1
| CHB | 84.7 | 10.9 | 4.4
| CHD | 86.2 | 6.4 | 7.3
| GIH | 75.2 | 9.9 | 14.9
| LWK | 48.6 | 25.7 | 25.7
| MEX | 75.9 | 19.0 | 5.2
| MKK | 54.5 | 20.5 | 25.0
| TSI | 52.0 | 22.5 | 25.5
| HapMapRevision=28
}}{{Venter SNP
|rsid=228406
|allele=C
|frequency=0.633
|uid=1103673020336
|type=homozygous_SNP
|hugo=DMD
|ensembl gene=ENSG00000198947
|ensembl transcript=ENST00000357033
|sift=TOLERATED
|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.
}}

{{PMID Auto
|PMID=18339804
|Title=X-inactivation in female human embryonic stem cells is in a nonrandom pattern and prone to epigenetic alterations.
|OA=1
}}

{{GET Evidence
|gene=DMD
|aa_change=Asp882Gly
|aa_change_short=D882G
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs228406
|overall_frequency_n=5693
|overall_frequency_d=8759
|overall_frequency=0.64996
|n_genomes=39
|n_genomes_annotated=0
|n_haplomes=71
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=4
|autoscore=3
|n_web_uneval=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}