{{Rsnum
|rsid=397515419
|Chromosome=1
|position=145917809
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX11B
|Gene_s=GNRHR2,PEX11B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000032935.1
|CLNALLE=1
|CLNDBN=Peroxisome biogenesis disorder 14B
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN160486:614920
|CLNHGVS=NC_000001.11:g.145917809G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_003846.2:c.64C>T; 603867.0001
|Disease=Peroxisome biogenesis disorder 14B
|FwdALT=T
|FwdREF=C
|GENEINFO=GNRHR2:114814; PEX11B:8799
|GENE_ID=114814; 8799
|GENE_NAME=GNRHR2; PEX11B
|REF=G
|RSPOS=145917809
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSN;REF;INT;R5;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x0500600a0605000002110100
|WGT=1
|dbSNPBuildID=136
|rsid=397515419
}}