{{Rsnum
|rsid=119103237
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALG3
|position=184245798
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALG3
}}{{omim
|id=608750
|rsnum=119103237
|variant=0004
}}{{ClinVar
|rsid=119103237
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=183963586
|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.183963586A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608750.0004
|CLNSIG=5
|CLNCUI=C1832736
|CLNDBN=Congenital disorder of glycosylation type 1D
|Disease=Congenital disorder of glycosylation type 1D
|CLNACC=RCV000002212.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1832736:601110:79321
}}