{{Rsnum
|rsid=387907221
|Chromosome=4
|position=55411783
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMEM165
|Gene_s=TMEM165
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=4
|CLNACC=RCV000029180.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 2k
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:CN130470:614727:314667
|CLNHGVS=NC_000004.11:g.56277950G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614726.0002
|Disease=Congenital disorder of glycosylation type 2k
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=56277950
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907221
|GENEINFO=TMEM165:55858
|GENE_ID=55858
|GENE_NAME=TMEM165
}}