{{Rsnum
|rsid=104894589
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MPDU1
|position=7585997
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MPDU1
}}{{omim
|id=604041
|rsnum=104894589
|variant=0005
}}{{ClinVar
|rsid=104894589
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=7489315
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MPDU1:9526
|GENE_NAME=MPDU1
|GENE_ID=9526
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.7489315T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604041.0005
|CLNSIG=5
|CLNCUI=C1836669
|CLNDBN=Congenital disorder of glycosylation type 1F
|Disease=Congenital disorder of glycosylation type 1F
|CLNACC=RCV000006229.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1836669:609180:79323
}}