{{Rsnum
|rsid=61750420
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PEX1
|position=92501562
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX1
}}{{omim
|id=602136
|rsnum=61750420
|variant=0001
}}

{{ClinVar
|rsid=61750420
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=92130876
|CHROM=7
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050160000000040002110100
|GENEINFO=PEX1:5189
|GENE_NAME=PEX1
|GENE_ID=5189
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.92130876C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=13801; 602136.0001
|CLNSIG=5
|CLNCUI=C0282527; C0282525; C0043459; C0339527
|CLNDBN=Peroxisome biogenesis disorders, Zellweger syndrome spectrum; Leber's amaurosis; Zellweger syndrome; not provided
|Disease=Peroxisome biogenesis disorders; Leber's amaurosis; Zellweger syndrome; not provided
|CLNACC=RCV000007946.2; RCV000022416.1; RCV000032927.1; RCV000078922.1
|Tags=RV;PM;SLO;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1448:C1832200:601539; NBK1298:C0339527:204000:193413001; NBK1448:C0043459:214100:912:88469006
}}

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