{{Rsnum
|rsid=2904551
|Gene=PRODH
|Chromosome=22
|position=18918421
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.002755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PRODH
}}{{omim
|desc=HYPERPROLINEMIA, TYPE I
|id=606810
|rsnum=2904551
|variant=0004
}}
{{ neighbor
| rsid = 3970559
| distance = 35
}}
{{ neighbor
| rsid = 2904552
| distance = 30
}}{{ClinVar
|rsid=2904551
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=18905934
|CHROM=22
|GMAF=0.0027
|dbSNPBuildID=101
|SSR=1
|SAO=1
|VP=0x050060000000040116110100
|GENEINFO=PRODH:5625
|GENE_NAME=PRODH
|GENE_ID=5625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.18905934A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606810.0004
|CLNSIG=255
|CLNCUI=C0268529
|CLNDBN=Proline dehydrogenase deficiency; Schizophrenia 4
|Disease=Proline dehydrogenase deficiency; Schizophrenia 4
|CLNACC=RCV000004218.1; RCV000004219.1
|Tags=PM;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9972; 0.002755
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM
|CLNDSDBID=C0268529:239500:419:61071003; C1833247:600850
|COMMON=1
}}