{{Rsnum
|rsid=146245480
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NEXN
|position=77926863
|Gene_s=NEXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000023985.1; RCV000041184.1
|CLNALLE=1
|CLNDBN=Familial hypertrophic cardiomyopathy 20; AllHighlyPenetrant
|CLNDSDB=MedGen:OMIM; MedGen
|CLNDSDBID=C3151267:613876; CN169374
|CLNHGVS=NC_000001.11:g.77926863C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_144573.3:c.835C>T; 613121.0005
|Disease=Familial hypertrophic cardiomyopathy 20; AllHighlyPenetrant
|FwdALT=T
|FwdREF=C
|GENEINFO=NEXN:91624
|GENE_ID=91624
|GENE_NAME=NEXN
|REF=C
|RSPOS=77926863
|Reversed=0
|SAO=0
|SSR=0
|Tags=NSM;REF;INT;ASP;KGPhase1;KGPROD;OTHERKG
|VC=SNV
|VP=0x050000080a05000016000100
|WGT=1
|dbSNPBuildID=134
|rsid=146245480
}}