{{Rsnum
|rsid = 28936677
|Gene = PPOX
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=1
|position=161166882
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PPOX
}}{{omim
|desc=VARIEGATE PORPHYRIA, HOMOZYGOUS
|id=600923
|rsnum=28936677
|variant=0012
}}

{{ClinVar
|rsid=28936677
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=161166882
|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.161166882T>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;NSM;REF;U5;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000009240.1; RCV000033939.2
|CLNDBN=Variegate porphyria, homozygous; Variegate porphyria
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK121283:C0162532:176200:ORPHA79473:58275005
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNSRCID=NM_001122764.1:c.35T>C; NBK121283; 600923.0012
|Disease=Variegate porphyria; Variegate porphyria
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}