{{Rsnum
|rsid=80356733
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=TARDBP
|position=11022451
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TARDBP
}}{{omim
|id=605078
|rsnum=80356733
|variant=0007
}}{{ClinVar
|rsid=80356733
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=11022451
|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
|CLNHGVS=NC_000001.11:g.11022451G>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_007375.3:c.1042G>T; NBK5942; 605078.0007
|CLNSIG=5
|CLNCUI=C2677565; C2677565
|CLNDBN=Amyotrophic lateral sclerosis type 10
|Disease=Amyotrophic lateral sclerosis type 10
|CLNACC=RCV000005545.3
|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=18372902
|Title=TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
}}

{{PMID Auto
|PMID=18779421
|Title=Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations.
|OA=1
}}