{{Rsnum
|rsid=267608255
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PEX7
|position=136845605
|Gene_s=PEX7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=6
|CLNACC=RCV000008229.1; RCV000032116.1
|CLNALLE=1
|CLNDBN=Peroxisome biogenesis disorder 9B; Phytanic acid storage disease
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=CN159238:614879:773; NBK1270:NBK1353:C0034960:266500:600964:773:25362006
|CLNHGVS=NC_000006.11:g.137166743A>G
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1270; 601757.0008
|Disease=Peroxisome biogenesis disorder 9B; Phytanic acid storage disease
|FwdALT=G
|FwdREF=A
|GENEINFO=PEX7:5191
|GENE_ID=5191
|GENE_NAME=PEX7
|REF=A
|RSPOS=137166743
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267608255
}}