{{Rsnum
|rsid=121918263
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=REEP1
|position=86252037
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=REEP1
}}{{omim
|id=609139
|rsnum=121918263
|variant=0005
}}{{ClinVar
|rsid=121918263
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=86479160
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=REEP1:65055
|GENE_NAME=REEP1
|GENE_ID=65055
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.86479160G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609139.0005
|CLNSIG=5
|CLNCUI=C1853247
|CLNDBN=Spastic paraplegia 31, autosomal dominant
|Disease=Spastic paraplegia 31
|CLNACC=RCV000001940.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853247:610250:101011
}}