{{Rsnum
|rsid=137852972
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BSCL2
|position=62702499
|Gene_s=BSCL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=606158
|variant=0013
|rsnum=137852972
}}{{ClinVar
|rsid=137852972
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=62469971
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=HNRNPUL2-BSCL2:100534595; BSCL2:26580
|GENE_NAME=HNRNPUL2-BSCL2; BSCL2
|GENE_ID=100534595; 26580
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.62469971T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606158.0013
|CLNSIG=5
|CLNCUI=C1833308
|CLNDBN=Silver spastic paraplegia syndrome; Distal hereditary motor neuronopathy type 5
|Disease=Silver spastic paraplegia syndrome; Distal hereditary motor neuronopathy type 5
|CLNACC=RCV000004801.3; RCV000004802.3
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C2931276; NBK1242:NBK1307:C1833308:600794:139536
}}