{{Rsnum
|rsid=140494585
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RTN2
|position=45489487
|Gene_s=RTN2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=19
|CLNACC=RCV000023261.1
|CLNALLE=1
|CLNDBN=Spastic paraplegia 12
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1858106:604805:100993
|CLNHGVS=NC_000019.9:g.45992745G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603183.0003
|Disease=Spastic paraplegia 12
|FwdALT=A
|FwdREF=G
|GENEINFO=RTN2:6253
|GENE_ID=6253
|GENE_NAME=RTN2
|REF=G
|RSPOS=45992745
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=140494585
}}