{{Rsnum
|rsid=121912789
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=CTSD
|position=1757343
|Gene_s=CTSD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=116840
|rsnum=121912789
|variant=0001
}}{{ClinVar
|rsid=121912789
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=1778573
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CTSD:1509
|GENE_NAME=CTSD
|GENE_ID=1509
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.1778573A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=116840.0001
|CLNSIG=5
|CLNCUI=C1864669
|CLNDBN=Ceroid lipofuscinosis neuronal 10
|Disease=Ceroid lipofuscinosis neuronal 10
|CLNACC=RCV000019134.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1428:C1864669:610127
}}