{{Rsnum
|rsid=121908138
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALS2
|position=201761524
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALS2
}}{{omim
|id=606352
|rsnum=121908138
|variant=0012
}}{{ClinVar
|rsid=121908138
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=202626247
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=ALS2:57679
|GENE_NAME=ALS2
|GENE_ID=57679
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.202626247C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1243; 606352.0012
|CLNSIG=5
|CLNCUI=C1846588
|CLNDBN=Infantile-onset ascending hereditary spastic paralysis
|Disease=Infantile-onset ascending hereditary spastic paralysis
|CLNACC=RCV000004665.3
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1243:C1846588:607225:293168
}}{{PMID Auto
|PMID=16718699
|Title=Novel missense mutation in ALS2 gene results in infantile ascending hereditary spastic paralysis.
}}