{{Rsnum
|rsid=104894489
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MPI
|position=74893306
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MPI
}}{{omim
|id=154550
|rsnum=104894489
|variant=0001
}}{{ClinVar
|rsid=104894489
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=75185647
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MPI:4351
|GENE_NAME=MPI
|GENE_ID=4351
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.75185647G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=154550.0001
|CLNSIG=5
|CLNCUI=C1865145
|CLNDBN=Congenital disorder of glycosylation type 1B
|Disease=Congenital disorder of glycosylation type 1B
|CLNACC=RCV000015419.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1865145:602579:79319
}}