{{Rsnum
|rsid=121908137
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALS2
|position=201726854
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALS2
}}{{omim
|id=606352
|rsnum=121908137
|variant=0010
}}{{ClinVar
|rsid=121908137
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=202591577
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=ALS2:57679
|GENE_NAME=ALS2
|GENE_ID=57679
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.202591577G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1243; 606352.0010
|CLNSIG=5
|CLNCUI=C1846588
|CLNDBN=Infantile-onset ascending hereditary spastic paralysis
|Disease=Infantile-onset ascending hereditary spastic paralysis
|CLNACC=RCV000004663.3
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1243:C1846588:607225:293168
}}{{PMID Auto
|PMID=12919135
|Title=The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings.
}}