{{Rsnum
|rsid=137853197
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NEXN
|position=77942756
|Gene_s=NEXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=613121
|variant=0002
|rsnum=137853197
}}{{ClinVar
|rsid=137853197
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=77942756
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=NEXN:91624
|GENE_NAME=NEXN
|GENE_ID=91624
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.77942756A>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_144573.3:c.1955A>G; 613121.0002
|CLNSIG=5
|CLNCUI=C2751084
|CLNDBN=Dilated cardiomyopathy 1CC; AllHighlyPenetrant
|Disease=Dilated cardiomyopathy 1CC; AllHighlyPenetrant
|CLNACC=RCV000000354.1; RCV000041170.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1309:C2751084:613122:ORPHA154; CN169374
}}