{{Rsnum
|rsid = 10742772
|Gene = PEX16
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=11
|position=45915716
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 3.0 | 97.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 3.0 | 97.0
| 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=10742772
|allele=T
|frequency=1
|uid=1103649676929
|type=homozygous_SNP
|hugo=PEX16
|ensembl gene=ENSG00000121680
|ensembl transcript=ENST00000241041
|sift=TOLERATED
|disease=Defects in PEX16 are a cause of peroxisome biogenesis disorder complementation group D (CGD) (MIM:603360); also known as Zellweger syndrome complementation group 9 (CG9).
}}

{{GET Evidence
|gene=PEX16
|aa_change=Val116Ile
|aa_change_short=V116I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10742772
|overall_frequency_n=128
|overall_frequency_d=128
|overall_frequency=1
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=112
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=2
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-4
|autoscore=3
|n_web_uneval=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}