{{Rsnum
|rsid=34154371
|Gene=PEX10
|Chromosome=1
|position=2406576
|Orientation=plus
|GMAF=0.009642
|Gene_s=PEX10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{PMID Auto
|PMID=15542397
|Title=The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.
}}{{ClinVar
|rsid=34154371
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=2338015
|CHROM=1
|GMAF=0.0096
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000a01040116100100
|GENEINFO=PEX10:5192
|GENE_NAME=PEX10
|GENE_ID=5192
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.10:g.2338015T>C
|CLNORIGIN=0
|CLNSIG=1
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9904; 0.009642
|RS=34154371
|COMMON=1
}}{{GET Evidence
|gene=PEX10
|aa_change=Thr294Ala
|aa_change_short=T294A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs34154371
|overall_frequency_n=1
|overall_frequency_d=128
|overall_frequency=0.0078125
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=1
|autoscore=3
|webscore=N
}}