{{Rsnum
|rsid=57965306
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=DES
|position=219421365
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DES
}}{{omim
|id=125660
|rsnum=57965306
|variant=0016
}}

{{ClinVar
|rsid=57965306
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=220286087
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=DES:1674
|GENE_NAME=DES
|GENE_ID=1674
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.220286087G>C
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=DES:c.1049G>C; 125660.0016
|CLNSIG=5
|CLNCUI=C1867005
|CLNDBN=Scapuloperoneal syndrome, neurogenic, Kaeser type; not provided
|Disease=Scapuloperoneal syndrome; not provided
|CLNACC=RCV000018329.22; RCV000056767.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1867005:181400
}}

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