{{Rsnum
|rsid=398122912
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PGM1
|position=63629539
|Gene_s=PGM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000032990.24
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1t
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN160489:614921
|CLNHGVS=NC_000001.11:g.63629539G>C
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001172819.1:c.-231G>C; NM_002633.2:c.361G>C; 171900.0003
|Disease=Congenital disorder of glycosylation type 1t
|FwdALT=C
|FwdREF=G
|GENEINFO=PGM1:5236
|GENE_ID=5236
|GENE_NAME=PGM1
|REF=G
|RSPOS=63629539
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;U5;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060400a05000002110100
|WGT=1
|dbSNPBuildID=138
|rsid=398122912
|CLNORIGIN=1
}}