{{Rsnum
|rsid=80356727
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TARDBP
|position=11022400
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TARDBP
}}{{omim
|id=605078
|rsnum=80356727
|variant=0002
}}{{ClinVar
|rsid=80356727
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=11022400
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050160000a05000002110100
|GENEINFO=TARDBP:23435
|GENE_NAME=TARDBP
|GENE_ID=23435
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.11022400C>A
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_007375.3:c.991C>A; NBK5942; 605078.0002
|CLNSIG=5
|CLNCUI=C2677565; C2677565
|CLNDBN=Amyotrophic lateral sclerosis type 10
|Disease=Amyotrophic lateral sclerosis type 10
|CLNACC=RCV000005540.1
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK5942:C2677565:612069:ORPHA275872:ORPHA803
}}