{{Rsnum
|rsid=387906316
|Chromosome=2
|position=201754672
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ALS2
|Gene_s=ALS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=2
|CLNACC=RCV000004659.2
|CLNALLE=1
|CLNDBN=Infantile-onset ascending hereditary spastic paralysis
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1243:C1846588:607225:293168
|CLNHGVS=NC_000002.11:g.202619395C>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1243; 606352.0006
|Disease=Infantile-onset ascending hereditary spastic paralysis
|FwdALT=T
|FwdREF=G
|REF=C
|RSPOS=202619395
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906316
|GENEINFO=ALS2:57679
|GENE_ID=57679
|GENE_NAME=ALS2
}}