{{Rsnum
|rsid=80356744
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TARDBP
|position=11022737
|Gene_s=TARDBP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356744
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=11022737
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168800005000002110100
|GENEINFO=TARDBP:23435
|GENE_NAME=TARDBP
|GENE_ID=23435
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.11022737T>C
|CLNSRC=ClinVar; GeneReviews
|CLNORIGIN=0
|CLNSRCID=NM_007375.3:c.*83T>C; NBK5942
|CLNSIG=5
|CLNCUI=C2677565
|CLNDBN=Amyotrophic lateral sclerosis type 10
|Disease=Amyotrophic lateral sclerosis type 10
|CLNACC=RCV000020654.1
|Tags=PM;PMC;SLO;U3;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK5942:C2677565:612069:ORPHA275872:ORPHA803
}}{{PMID Auto
|PMID=18931000
|Title=Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.
}}