{{Rsnum
|rsid=121908583
|Chromosome=20
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=DPM1
|position=50948650
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DPM1
}}{{omim
|id=603503
|rsnum=121908583
|variant=0001
}}{{ClinVar
|rsid=121908583
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=49565187
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=DPM1:8813
|GENE_NAME=DPM1
|GENE_ID=8813
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.49565187G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603503.0001
|CLNSIG=5
|CLNCUI=C1837396
|CLNDBN=Congenital disorder of glycosylation type 1E
|Disease=Congenital disorder of glycosylation type 1E
|CLNACC=RCV000006676.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1837396:608799:79322
}}