{{Rsnum
|rsid=41270025
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PPOX
|position=161168463
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PPOX
}}{{omim
|id=600923
|rsnum=41270025
|variant=0006
}}

{{ClinVar
|rsid=41270025
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=161168463
|CHROM=1
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050260000a05000102110100
|GENEINFO=PPOX:5498
|GENE_NAME=PPOX
|GENE_ID=5498
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.161168463G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001122764.1:c.503G>A; 600923.0006
|CLNSIG=5
|CLNCUI=C0162532
|CLNDBN=Variegate porphyria
|Disease=Variegate porphyria
|CLNACC=RCV000009234.2
|Tags=PM;S3D;NSM;REF;ASP;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK121283:C0162532:176200:ORPHA79473:58275005
}}

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