{{Rsnum
|rsid=104894206
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CTSC
|position=88309176
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CTSC
}}{{omim
|id=602365
|rsnum=104894206
|variant=0001
}}{{ClinVar
|rsid=104894206
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=88042344
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CTSC:1075
|GENE_NAME=CTSC
|GENE_ID=1075
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.88042344G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602365.0001
|CLNSIG=5
|CLNCUI=C0030360
|CLNDBN=Papillon-LefÃ¨vre syndrome
|Disease=Papillon-LefÃ¨vre syndrome
|CLNACC=RCV000007712.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0030360:245000:678:40158001
}}