{{Rsnum
|rsid=397515327
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=DPAGT1
|position=119100785
|Gene_s=DPAGT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000055659.22
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1J
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1842572:608093:86309
|CLNHGVS=NC_000011.9:g.118971495G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=191350.0009
|Disease=Congenital disorder of glycosylation type 1J
|FwdALT=G
|FwdREF=C
|GENEINFO=DPAGT1:1798
|GENE_ID=1798
|GENE_NAME=DPAGT1
|REF=G
|RSPOS=118971495
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515327
}}