{{Rsnum
|rsid=80356737
|Chromosome=1
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=TARDBP
|position=11022530
|Gene_s=TARDBP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356737
|Reversed=0
|FwdREF=TAT
|FwdALT=A
|REF=T
|ALT=TA
|RSPOS=11022529
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168001205000002110200
|GENEINFO=TARDBP:23435
|GENE_NAME=TARDBP
|GENE_ID=23435
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.11022530dupA
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=612069
|CLNDBN=Amyotrophic lateral sclerosis type 10
|Tags=PM;PMC;SLO;NSF;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000020660.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK5942:C2677565:612069:ORPHA275872:ORPHA803
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_007375.3:c.1121_1122insA; NBK5942
|Disease=Amyotrophic lateral sclerosis type 10
}}{{PMID Auto
|PMID=18931000
|Title=Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.
}}