{{Rsnum
|rsid = 28942090
|Gene = ALG12
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=G
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=22
|position=49910479
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALG12
}}{{omim
|desc=CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig
|id=607144
|rsnum=28942090
|variant=0001
}}

{{ClinVar
|rsid=28942090
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=50304127
|CHROM=22
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ALG12:79087
|GENE_NAME=ALG12
|GENE_ID=79087
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.50304127A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607144.0001
|CLNSIG=5
|CLNCUI=C1846695
|CLNDBN=Congenital disorder of glycosylation type 1G
|Disease=Congenital disorder of glycosylation type 1G
|CLNACC=RCV000003602.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1846695:607143:79324
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}