{{Rsnum
|rsid=121917725
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEPD
|position=33411697
|Gene_s=PEPD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=613230
|rsnum=121917725
|variant=0008
}}{{ClinVar
|rsid=121917725
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=33902603
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PEPD:5184
|GENE_NAME=PEPD
|GENE_ID=5184
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.33902603G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613230.0008
|CLNSIG=5
|CLNCUI=C0268532
|CLNDBN=Prolidase deficiency
|Disease=Prolidase deficiency
|CLNACC=RCV000000239.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0268532:170100:742
}}