{{Rsnum
|rsid=387906264
|Chromosome=2
|position=86254816
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=REEP1
|Gene_s=REEP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=2
|CLNACC=RCV000001937.1
|CLNALLE=1
|CLNDBN=Spastic paraplegia 31, autosomal dominant
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853247:610250:101011
|CLNHGVS=NC_000002.11:g.86481939T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609139.0002
|Disease=Spastic paraplegia 31
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=86481939
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906264
|GENEINFO=REEP1:65055
|GENE_ID=65055
|GENE_NAME=REEP1
}}