{{Rsnum
|rsid=387907079
|Chromosome=1
|position=77918217
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NEXN
|Gene_s=NEXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=1
|CLNACC=RCV000023984.1
|CLNALLE=1
|CLNDBN=Familial hypertrophic cardiomyopathy 20
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151267:613876
|CLNHGVS=NC_000001.11:g.77918217C>G
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_144573.3:c.391C>G; 613121.0004
|Disease=Familial hypertrophic cardiomyopathy 20
|FwdALT=G
|FwdREF=C
|REF=C
|RSPOS=77918217
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387907079
|GENEINFO=NEXN:91624
|GENE_ID=91624
|GENE_NAME=NEXN
|CLNORIGIN=1
}}