{{Rsnum
|rsid=121913013
|Gene=DSG2
|Chromosome=18
|position=31519887
|Orientation=plus
|GMAF=0.0004591
|Gene_s=DSG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|id=125671
|rsnum=121913013
|variant=0009
}}{{ClinVar
|rsid=121913013
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=29099850
|CHROM=18
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=DSG2:1829
|GENE_NAME=DSG2
|GENE_ID=1829
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.29099850G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=125671.0009
|CLNSIG=255
|CLNCUI=C1857777
|CLNDBN=Arrhythmogenic right ventricular cardiomyopathy, type 10; Cardiomyopathy, dilated, 1bb, susceptibility to; AllHighlyPenetrant
|Disease=Arrhythmogenic right ventricular cardiomyopathy; Cardiomyopathy; AllHighlyPenetrant
|CLNACC=RCV000018311.22; RCV000018312.1; RCV000037270.1
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=NBK1131:C1857777:610193; CN169374
|COMMON=0
}}