{{Rsnum
|rsid=386134173
|Chromosome=2
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=ALS2
|position=201767266
|Gene_s=ALS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=2
|CLNACC=RCV000004655.3
|CLNALLE=1
|CLNDBN=Amyotrophic lateral sclerosis type 2
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1243:NBK1450:C1859807:205100:300605
|CLNHGVS=NC_000002.11:g.202631989delT
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1243; 606352.0001
|Disease=Amyotrophic lateral sclerosis type 2
|FwdREF=A
|REF=CT
|RSPOS=202631988
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386134173
|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.
}}

{{PMID Auto
|PMID=11586298
|Title=A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
}}