{{Rsnum
|rsid=80356715
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TARDBP
|position=11016874
|Gene_s=TARDBP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356715
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=11016874
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000a05040002100100
|GENEINFO=TARDBP:23435
|GENE_NAME=TARDBP
|GENE_ID=23435
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.11016874C>T
|CLNSRC=ClinVar; GeneReviews
|CLNORIGIN=0
|CLNSRCID=NM_007375.3:c.269C>T; NBK5942
|CLNSIG=2
|CLNCUI=C2677565
|CLNDBN=Amyotrophic lateral sclerosis type 10
|Disease=Amyotrophic lateral sclerosis type 10
|CLNACC=RCV000020670.1
|Tags=PM;PMC;S3D;SLO;NSM;REF;ASP;VLD;OTHERKG;LSD
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK5942:C2677565:612069:ORPHA275872:ORPHA803
}}{{PMID|18309045}} TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.

{{PMID|18372902}} TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.

{{PMID|18505686|OA=1
}} A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro.

{{PMID|18545701|OA=1
}} TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis.