{{Rsnum
|rsid=121909484
|Chromosome=3
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SLC33A1
|position=155853659
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC33A1
}}{{omim
|id=603690
|rsnum=121909484
|variant=0001
}}{{ClinVar
|rsid=121909484
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=155571448
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SLC33A1:9197
|GENE_NAME=SLC33A1
|GENE_ID=9197
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.155571448A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603690.0001
|CLNSIG=5
|CLNCUI=C2675528
|CLNDBN=Spastic paraplegia 42, autosomal dominant
|Disease=Spastic paraplegia 42
|CLNACC=RCV000006506.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2675528:612539:171863
}}