{{Rsnum
|rsid = 28939378
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Gene = ALG1
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=16
|position=5078789
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALG1
}}{{omim
|desc=CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik
|id=605907
|rsnum=28939378
|variant=0001
}}

{{ClinVar
|rsid=28939378
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=5128790
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ALG1:56052
|GENE_NAME=ALG1
|GENE_ID=56052
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.5128790C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=5852; 605907.0001
|CLNSIG=5
|CLNCUI=C1837896
|CLNDBN=Congenital disorder of glycosylation type 1K; not provided
|Disease=Congenital disorder of glycosylation type 1K; not provided
|CLNACC=RCV000004989.1; RCV000081987.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1837896:608540:79327
}}

{{on chip | 23andMe v1}}