{{Rsnum
|rsid=121918371
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PGM1
|position=63629521
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PGM1
}}{{omim
|id=171900
|rsnum=121918371
|variant=0001
}}{{ClinVar
|rsid=121918371
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=63629521
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260400a05000002110100
|GENEINFO=PGM1:5236
|GENE_NAME=PGM1
|GENE_ID=5236
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.63629521A>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001172819.1:c.-249A>G; NM_002633.2:c.343A>G; 171900.0001
|CLNSIG=5
|CLNCUI=C2752015
|CLNDBN=Congenital disorder of glycosylation type 1t
|Disease=Congenital disorder of glycosylation type 1t
|CLNACC=RCV000014620.25
|Tags=PM;S3D;NSM;REF;U5;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN160489:614921
}}