{{Rsnum
|rsid=367543041
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TARDBP
|position=11022553
|Gene_s=TARDBP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,C
|CHROM=1
|CLNACC=RCV000020663.4; RCV000106321.1; RCV000020664.1
|CLNALLE=1; 2
|CLNDBN=Amyotrophic lateral sclerosis type 10; FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK5942:C2677565:612069:ORPHA275872:ORPHA803
|CLNHGVS=NC_000001.11:g.11022553G>A; NC_000001.11:g.11022553G>C
|CLNORIGIN=1; 0
|CLNSIG=5
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNSRCID=NM_007375.3:c.1144G>A; NBK5942; 605078.0013; NM_007375.3:c.1144G>C
|Disease=Amyotrophic lateral sclerosis type 10; FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS
|FwdALT=A,C
|FwdREF=G
|REF=G
|RSPOS=11022553
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=367543041
|GENEINFO=TARDBP:23435
|GENE_ID=23435
|GENE_NAME=TARDBP
}}{{PMID Auto
|PMID=18372902
|Title=TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
}}

{{PMID Auto
|PMID=19224587
|Title=High frequency of TARDBP gene mutations in Italian patients with 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.
}}