{{Rsnum
|rsid=121912790
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CTSD
|position=1753593
|Gene_s=CTSD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=116840
|rsnum=121912790
|variant=0002
}}{{ClinVar
|rsid=121912790
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=1774823
|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.1774823C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=116840.0002
|CLNSIG=5
|CLNCUI=C1864669
|CLNDBN=Ceroid lipofuscinosis neuronal 10
|Disease=Ceroid lipofuscinosis neuronal 10
|CLNACC=RCV000019135.22
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1428:C1864669:610127
}}