{{Rsnum
|rsid=387906281
|Chromosome=9
|position=99218145
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=ALG2
|Gene_s=ALG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=9
|CLNACC=RCV000002818.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1I
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1842836:607906:79326
|CLNHGVS=NC_000009.11:g.101980427delC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607905.0001
|Disease=Congenital disorder of glycosylation type 1I
|FwdREF=G
|REF=AC
|RSPOS=101980426
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906281
|GENEINFO=ALG2:85365
|GENE_ID=85365
|GENE_NAME=ALG2
}}