{{Rsnum
|rsid=121908022
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALG9
|position=111836179
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALG9
}}{{omim
|id=606941
|rsnum=121908022
|variant=0001
}}{{ClinVar
|rsid=121908022
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=111706902
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ALG9:79796
|GENE_NAME=ALG9
|GENE_ID=79796
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.111706902C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606941.0001
|CLNSIG=5
|CLNCUI=C1837438
|CLNDBN=Congenital disorder of glycosylation type 1L
|Disease=Congenital disorder of glycosylation type 1L
|CLNACC=RCV000003946.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1837438:608776:79328
}}