{{Rsnum
|rsid=121918326
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PPOX
|position=161166906
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PPOX
}}{{omim
|id=600923
|rsnum=121918326
|variant=0005
}}{{ClinVar
|rsid=121918326
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=161166906
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260400a05000002110100
|GENEINFO=PPOX:5498
|GENE_NAME=PPOX
|GENE_ID=5498
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.161166906A>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001122764.1:c.59A>C; 600923.0005
|CLNSIG=5
|CLNCUI=C0162532
|CLNDBN=Variegate porphyria
|Disease=Variegate porphyria
|CLNACC=RCV000009232.1
|Tags=PM;S3D;NSM;REF;U5;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK121283:C0162532:176200:ORPHA79473:58275005
}}