{{Rsnum
|rsid=386134181
|Chromosome=2
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CT)
|geno3=(CT;CT)
|Gene=ALS2
|position=201746696
|Gene_s=ALS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=2
|CLNACC=RCV000004656.3
|CLNALLE=1
|CLNDBN=Juvenile primary lateral sclerosis
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1243:C1853396:606353:247604
|CLNHGVS=NC_000002.11:g.202611419_202611420delAG
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1243; 606352.0002
|Disease=Juvenile primary lateral sclerosis
|FwdREF=CT
|REF=CAG
|RSPOS=202611418
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386134181
|GENEINFO=ALS2:57679
|GENE_ID=57679
|GENE_NAME=ALS2
}}{{PMID Auto
|PMID=11586297
|Title=The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
}}