{{Rsnum
|rsid = 28939094
|Gene=ATL1
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=14
|position=50628133
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATL1
}}{{omim
|desc=SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT
|id=606439
|rsnum=28939094
|variant=0006
}}

{{ClinVar
|rsid=28939094
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=51094851
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=ATL1:51062
|GENE_NAME=ATL1
|GENE_ID=51062
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.51094851A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK45978; 606439.0006
|CLNSIG=5
|CLNCUI=CN074283; CN074283
|CLNDBN=Spastic paraplegia 3
|Disease=Spastic paraplegia 3
|CLNACC=RCV000004599.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK45978:CN074283:182600
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}