{{Rsnum
|rsid=11689432
|Gene=TARDBP
|Chromosome=2
|position=238232864
|Orientation=plus
|GMAF=0.4679
|Gene_s=TARDBP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 27.7 | 49.2 | 23.1
| HCB | 37.8 | 55.6 | 6.7
| JPT | 36.4 | 50.0 | 13.6
| YRI | 11.1 | 38.1 | 50.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 37.8 | 55.6 | 6.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{ClinVar
|rsid=11689432
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=11082610
|CHROM=1
|dbSNPBuildID=120
|SSR=0
|SAO=0
|VP=050168000a0507051f110100
|GENEINFO=TARDBP:23435
|GENE_NAME=TARDBP
|GENE_ID=23435
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.10:g.11082610G>A; NC_000001.10:g.11082610G>C
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK5942
|CLNSIG=5
|CLNCUI=C2677565
|CLNDBN=Amyotrophic lateral sclerosis type 10
|Disease=Amyotrophic lateral sclerosis type 10
|CLNACC=SCV000041201.1; SCV000041202.1
|Tags=PM;PMC;SLO;NSM;REF;ASP;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
}}{{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.
}}
{{omim
|id=612069
|rsnum=11689432
}}