{{Rsnum
|rsid=104894495
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MPI
|position=74892728
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MPI
}}{{omim
|id=154550
|rsnum=104894495
|variant=0003
}}{{ClinVar
|rsid=104894495
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=75185069
|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.75185069T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=154550.0003
|CLNSIG=5
|CLNCUI=C1865145
|CLNDBN=Congenital disorder of glycosylation type 1B
|Disease=Congenital disorder of glycosylation type 1B
|CLNACC=RCV000015421.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1865145:602579:79319
}}