{{Rsnum
|rsid=387906959
|Chromosome=13
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=COG6
|position=39723394
|Gene_s=COG6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=13
|CLNACC=RCV000023603.3
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 2l
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN124732:614576
|CLNHGVS=NC_000013.10:g.40297531G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606977.0001
|Disease=Congenital disorder of glycosylation type 2l
|FwdALT=T
|FwdREF=G
|REF=G
|RSPOS=40297531
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906959
|GENEINFO=COG6:57511
|GENE_ID=57511
|GENE_NAME=COG6
}}