{{Rsnum
|rsid = 28936676
|Gene = PPOX
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=C
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=1
|position=161170467
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PPOX
}}{{omim
| id = 600923
| variant = 0007
| desc    = VARIEGATE PORPHYRIA, HOMOZYGOUS
| rsnum   = 28936676
}}

{{ClinVar
|rsid=28936676
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=161170467
|CHROM=1
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260080a05000402110100
|GENEINFO=PPOX:5498
|GENE_NAME=PPOX
|GENE_ID=5498
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.161170467A>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;NSM;REF;INT;ASP;HD;OTHERKG;LSD;OM
|CLNACC=RCV000009235.1
|CLNDBN=Variegate porphyria, homozygous
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001122764.1:c.1046A>C; 600923.0007
|Disease=Variegate porphyria
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}