{{Rsnum
|rsid=104894532
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PMM2
|position=8797908
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PMM2,TMEM186
}}{{omim
|id=601785
|rsnum=104894532
|variant=0015
}}{{ClinVar
|rsid=104894532
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=8891765
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TMEM186:25880; PMM2:5373
|GENE_NAME=TMEM186; PMM2
|GENE_ID=25880; 5373
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.8891765G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601785.0015
|CLNSIG=5
|CLNCUI=C0349653
|CLNDBN=Carbohydrate-deficient glycoprotein syndrome type I
|Disease=Carbohydrate-deficient glycoprotein syndrome type I
|CLNACC=RCV000008159.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1110:NBK1332:C0349653:212065:79318:277893002
}}