{{Rsnum
|rsid=200314808
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ATL1
|position=50587992
|Gene_s=ATL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=14
|CLNACC=RCV000023543.2
|CLNALLE=1
|CLNDBN=NEUROPATHY, HEREDITARY SENSORY, TYPE ID
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3150972:613708:36386
|CLNHGVS=NC_000014.8:g.51054710G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606439.0011
|Disease=NEUROPATHY
|FwdALT=C
|FwdREF=G
|GENEINFO=ATL1:51062
|GENE_ID=51062
|GENE_NAME=ATL1
|REF=G
|RSPOS=51054710
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=200314808
}}