{{Rsnum
|rsid=121908443
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALG6
|position=63419380
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALG6
}}{{omim
|id=604566
|rsnum=121908443
|variant=0001
}}{{ClinVar
|rsid=121908443
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=63419380
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=ALG6:29929
|GENE_NAME=ALG6
|GENE_ID=29929
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.63419380C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_013339.3:c.998C>T; 604566.0001
|CLNSIG=5
|CLNCUI=C1864178
|CLNDBN=Congenital disorder of glycosylation type 1C
|Disease=Congenital disorder of glycosylation type 1C
|CLNACC=RCV000005832.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1864178:603147:ORPHA79320
}}