{{Rsnum
|rsid=121908294
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALG8
|position=78112724
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALG8
}}{{omim
|id=608103
|rsnum=121908294
|variant=0006
}}{{ClinVar
|rsid=121908294
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=77823770
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ALG8:79053
|GENE_NAME=ALG8
|GENE_ID=79053
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.77823770C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608103.0006
|CLNSIG=5
|CLNCUI=C1842539
|CLNDBN=Congenital disorder of glycosylation type 1H
|Disease=Congenital disorder of glycosylation type 1H
|CLNACC=RCV000002672.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1842539:608104:79325
}}