{{Rsnum
|rsid=12941376
|Gene=PEX12
|Chromosome=17
|position=35576129
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=A
|GMAF=0.008724
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=PEX12
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 91.8 | 8.2 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=12941376
|allele=T
|frequency=
|uid=1103645314318
|type=heterozygous_SNP
|hugo=PEX12
|ensembl gene=ENSG00000108733
|ensembl transcript=ENST00000225873
|sift=TOLERATED
|disease=Defects in PEX12 are a cause of Zellweger syndrome (ZS) (MIM:214100); a severe peroxisome biogenesis disorder.
}}

{{ neighbor
| rsid = 28936697
| distance = 226
}}

{{GET Evidence
|gene=PEX12
|aa_change=Leu245Ile
|aa_change_short=L245I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12941376
|overall_frequency_n=130
|overall_frequency_d=10758
|overall_frequency=0.012084
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-2
|autoscore=3
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}