{{Rsnum
|rsid=121917724
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PEPD
|position=33387892
|Gene_s=PEPD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=613230
|rsnum=121917724
|variant=0005
}}{{ClinVar
|rsid=121917724
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=33878798
|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.33878798C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613230.0005
|CLNSIG=5
|CLNCUI=C0268532
|CLNDBN=Prolidase deficiency
|Disease=Prolidase deficiency
|CLNACC=RCV000000237.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0268532:170100:742
}}