{{Rsnum
|rsid=121907933
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALG12
|position=49910602
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALG12
}}{{omim
|id=607144
|rsnum=121907933
|variant=0004
}}{{ClinVar
|rsid=121907933
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50304250
|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.50304250C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607144.0004
|CLNSIG=5
|CLNCUI=C1846695
|CLNDBN=Congenital disorder of glycosylation type 1G
|Disease=Congenital disorder of glycosylation type 1G
|CLNACC=RCV000003605.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1846695:607143:79324
}}