{{Rsnum
|rsid=34417028
|Gene=DSG2
|Chromosome=18
|position=31546033
|Orientation=plus
|GMAF=0.004132
|Gene_s=AGPAT6,DSG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=34417028
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=29125996
|CHROM=18
|GMAF=0.0041
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050160000000000116100100
|GENEINFO=RP11-75N4.2:100652770; DSG2:1829
|GENE_NAME=RP11-75N4.2; DSG2
|GENE_ID=100652770; 1829
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.29125996T>C
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Cardiomyopathy; AllHighlyPenetrant
|Disease=Cardiomyopathy; AllHighlyPenetrant
|Tags=PM;SLO;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9959; 0.004132
|CLNACC=RCV000029669.1; RCV000037291.1
|CLNDSDB=MedGen:SNOMED_CT; MedGen
|CLNDSDBID=C0878544:85898001; CN169374
|COMMON=1
}}{{GET Evidence
|gene=DSG2
|aa_change=Ser883Pro
|aa_change_short=S883P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs34417028
|overall_frequency_n=57
|overall_frequency_d=9652
|overall_frequency=0.00590551
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.239
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=3
|autoscore=3
|webscore=N
}}