{{Rsnum
|rsid=121434591
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MATR3
|position=139307669
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MATR3
}}{{omim
|id=164015
|rsnum=121434591
|variant=0001
}}{{ClinVar
|rsid=121434591
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=138643358
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=MATR3:9782
|GENE_NAME=MATR3
|GENE_ID=9782
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.138643358C>G
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=164015.0001; VAR_063421
|CLNSIG=255
|CLNCUI=C1853723
|CLNDBN=Myopathy, distal, 2
|Disease=Myopathy
|CLNACC=RCV000015039.26
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853723:606070:600
}}{{PMID Auto
|PMID=19344878
|Title=Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.
|OA=1
}}