{{Rsnum
|rsid=104894446
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MGAT2
|position=49622137
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MGAT2,RPL36AL
}}{{omim
|id=602616
|rsnum=104894446
|variant=0001
}}{{ClinVar
|rsid=104894446
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=50088855
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MGAT2:4247; RPL36AL:6166
|GENE_NAME=MGAT2; RPL36AL
|GENE_ID=4247; 6166
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.50088855C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602616.0001
|CLNSIG=5
|CLNCUI=C0349654
|CLNDBN=Carbohydrate-deficient glycoprotein syndrome type II
|Disease=Carbohydrate-deficient glycoprotein syndrome type II
|CLNACC=RCV000007405.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1332:C0349654:212066:79329:277894008
}}