{{Rsnum
|rsid=267606929
|Chromosome=10
|position=13132098
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OPTN
|Gene_s=OPTN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=G
|CHROM=10
|CLNACC=RCV000007520.1
|CLNALLE=1
|CLNDBN=Amyotrophic lateral sclerosis type 12
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1450:C3150692:613435:803
|CLNHGVS=NC_000010.10:g.13174098A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602432.0007
|Disease=Amyotrophic lateral sclerosis type 12
|FwdALT=G
|FwdREF=A
|GENEINFO=OPTN:10133
|GENE_ID=10133
|GENE_NAME=OPTN
|REF=A
|RSPOS=13174098
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606929
}}