{{Rsnum
|rsid=397704705
|Chromosome=7
|Orientation=plus
|geno1=(GGAT;GGAT)
|geno2=(GGAT;TGCTGTAAACTGTAACTGTAAA)
|geno3=(TGCTGTAAACTGTAACTGTAAA;TGCTGTAAACTGTAACTGTAAA)
|Gene=AP5Z1
|position=4781213
|Gene_s=AP5Z1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CTGCTGTAAACTGTAACTGTAAA
|CHROM=7
|CLNACC=RCV000000012.1
|CLNALLE=1
|CLNDBN=Spastic paraplegia 48, autosomal recessive
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3150901:613647:306511
|CLNHGVS=NC_000007.13:g.4820844_4820847delGGATinsTGCTGTAAACTGTAACTGTAAA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613653.0001
|Disease=Spastic paraplegia 48
|FwdALT=TGCTGTAAACTGTAACTGTAAA
|FwdREF=GGAT
|GENEINFO=AP5Z1:9907
|GENE_ID=9907
|GENE_NAME=AP5Z1
|REF=CGGAT
|RSPOS=4820843
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=397704705
}}