{{Rsnum
|rsid = 28934876
|Gene = DPAGT1
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=11
|position=119100396
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DPAGT1
}}{{omim
|desc=CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij
|id=191350
|rsnum=28934876
|variant=0001
}}

{{ClinVar
|rsid=28934876
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=118971106
|CHROM=11
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=DPAGT1:1798
|GENE_NAME=DPAGT1
|GENE_ID=1798
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.118971106T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191350.0001
|CLNSIG=5
|CLNCUI=C1842572
|CLNDBN=Congenital disorder of glycosylation type 1J
|Disease=Congenital disorder of glycosylation type 1J
|CLNACC=RCV000013090.21
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1842572:608093:86309
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}