{{Rsnum
|rsid=397515423
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PGM1
|position=63654374
|Gene_s=PGM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000032991.24
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1t
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN160489:614921
|CLNHGVS=NC_000001.11:g.63654374C>T
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_002633.2:c.1507C>T; 171900.0004
|Disease=Congenital disorder of glycosylation type 1t
|FwdALT=T
|FwdREF=C
|GENEINFO=PGM1:5236
|GENE_ID=5236
|GENE_NAME=PGM1
|REF=C
|RSPOS=63654374
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSN;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000605000002110100
|WGT=1
|dbSNPBuildID=136
|rsid=397515423
|CLNORIGIN=1
}}