{{Rsnum
|rsid = 28928906
|Gene = MPI
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=15
|position=74897050
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MPI
}}{{omim
|desc=CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib
|id=154550
|rsnum=28928906
|variant=0005
}}

{{ClinVar
|rsid=28928906
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=75189391
|CHROM=15
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=MPI:4351
|GENE_NAME=MPI
|GENE_ID=4351
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.75189391G>A
|CLNSRC=GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000237318; 154550.0005
|CLNSIG=5
|CLNCUI=C1865145
|CLNDBN=Congenital disorder of glycosylation type 1B
|Disease=Congenital disorder of glycosylation type 1B
|CLNACC=RCV000015423.25
|Tags=PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1865145:602579:79319
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}