{{Rsnum
|rsid=121908155
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DPM3
|position=155139987
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DPM3
}}{{omim
|id=605951
|rsnum=121908155
|variant=0001
}}{{ClinVar
|rsid=121908155
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=155139987
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000a05000002110100
|GENEINFO=DPM3:54344
|GENE_NAME=DPM3
|GENE_ID=54344
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.155139987A>G
|CLNSRC=ClinVar; Leiden Muscular Dystrophy pages (DPM3); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_153741.1:c.254T>C; DPM3_00001; 605951.0001
|CLNSIG=5
|CLNCUI=C2752007
|CLNDBN=Congenital disorder of glycosylation type 1O
|Disease=Congenital disorder of glycosylation type 1O
|CLNACC=RCV000004967.1
|Tags=RV;PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C2752007:612937:ORPHA263494
}}{{PMID Auto
|PMID=19576565
|Title=Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies.
|OA=1
}}