{{Rsnum
|rsid=387907203
|Chromosome=16
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=COG4
|position=70481062
|Gene_s=COG4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=16
|CLNACC=RCV000024609.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 2J
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C3150736:613489:263501
|CLNHGVS=NC_000016.9:g.70514965A>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606976.0004
|Disease=Congenital disorder of glycosylation type 2J
|FwdALT=G
|FwdREF=T
|REF=A
|RSPOS=70514965
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907203
|GENEINFO=COG4:25839
|GENE_ID=25839
|GENE_NAME=COG4
}}