{{Rsnum
|rsid = 28940588
|Gene = ALG3
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=3
|position=184245559
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALG3
}}{{omim
|desc=CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id
|id=608750
|rsnum=28940588
|variant=0001
}}

{{ClinVar
|rsid=28940588
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=183963347
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ALG3:10195
|GENE_NAME=ALG3
|GENE_ID=10195
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.183963347C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608750.0001
|CLNSIG=5
|CLNCUI=C1832736
|CLNDBN=Congenital disorder of glycosylation type 1D
|Disease=Congenital disorder of glycosylation type 1D
|CLNACC=RCV000002209.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1832736:601110:79321
}}

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