{{Rsnum
|rsid=80356721
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TARDBP
|position=11022290
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TARDBP
}}{{omim
|id=605078
|rsnum=80356721
|variant=0003
}}{{ClinVar
|rsid=80356721
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=11022290
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000a05000002110100
|GENEINFO=TARDBP:23435
|GENE_NAME=TARDBP
|GENE_ID=23435
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.11022290G>C; NC_000001.11:g.11022290G>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1; 0
|CLNSRCID=NM_007375.3:c.881G>C; NBK5942; 605078.0003; NM_007375.3:c.881G>T
|CLNSIG=5
|CLNCUI=C2677565; C2677565,C2677565
|CLNDBN=Amyotrophic lateral sclerosis type 10
|Disease=Amyotrophic lateral sclerosis type 10
|CLNACC=RCV000005541.1; RCV000020673.1
|Tags=PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK5942:C2677565:612069:ORPHA275872:ORPHA803
}}{{PMID Auto
|PMID=18309045
|Title=TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.
}}

{{PMID Auto
|PMID=19236453
|Title=TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
}}