{{Rsnum
|rsid=104894448
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MGAT2
|position=49622220
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MGAT2,RPL36AL
}}{{omim
|id=602616
|rsnum=104894448
|variant=0003
}}{{ClinVar
|rsid=104894448
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=50088938
|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.50088938A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602616.0003
|CLNSIG=5
|CLNCUI=C0349654
|CLNDBN=Carbohydrate-deficient glycoprotein syndrome type II
|Disease=Carbohydrate-deficient glycoprotein syndrome type II
|CLNACC=RCV000007407.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1332:C0349654:212066:79329:277894008
}}