{{Rsnum
|rsid=80356717
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TARDBP
|position=11018836
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TARDBP
}}{{omim
|id=605078
|rsnum=80356717
|variant=0006
}}{{ClinVar
|rsid=80356717
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=11018836
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000a05000002110100
|GENEINFO=TARDBP:23435
|GENE_NAME=TARDBP
|GENE_ID=23435
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.11018836A>G
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_007375.3:c.506A>G; NBK5942; 605078.0006
|CLNSIG=5
|CLNCUI=C2677565; C2677565
|CLNDBN=Amyotrophic lateral sclerosis type 10
|Disease=Amyotrophic lateral sclerosis type 10
|CLNACC=RCV000005544.3
|Tags=PM;PMC;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK5942:C2677565:612069:ORPHA275872:ORPHA803
}}{{PMID|18372902}} TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.