{{Rsnum
|rsid=121909291
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MOGS
|position=74462332
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MOGS
}}{{omim
|id=601336
|rsnum=121909291
|variant=0001
}}{{ClinVar
|rsid=121909291
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=74689459
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MOGS:7841
|GENE_NAME=MOGS
|GENE_ID=7841
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.74689459C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601336.0001
|CLNSIG=5
|CLNCUI=C1853736
|CLNDBN=Congenital disorder of glycosylation type 2B
|Disease=Congenital disorder of glycosylation type 2B
|CLNACC=RCV000008676.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1853736:606056:79330
}}