{{Rsnum
|rsid=35383149
|Gene=ALG6
|Chromosome=1
|position=63406361
|Orientation=plus
|GMAF=0.01791
|Gene_s=ALG6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=C
|CAF=0.9821; 0.01791
|CHROM=1
|CLNACC=RCV000023375.1; RCV000081558.3
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1C; AllHighlyPenetrant
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1864178:603147:ORPHA79320
|CLNHGVS=NC_000001.11:g.63406361T>C
|CLNSIG=255
|CLNSRC=ClinVar; Emory University; University of Chicago; OMIM Allelic Variant
|CLNSRCID=NM_013339.3:c.391T>C; 5650; NM_013339.3(ALG6):c.391T; 604566.0007
|COMMON=1
|Disease=Congenital disorder of glycosylation type 1C; AllHighlyPenetrant
|FwdALT=G
|FwdREF=A
|GENEINFO=ALG6:29929
|GENE_ID=29929
|GENE_NAME=ALG6
|REF=T
|RSPOS=63406361
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;NSM;REF;ASP;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM;NOC
|VC=SNV
|VP=0x050160000a05140516110110
|WGT=1
|dbSNPBuildID=126
|rsid=35383149
|CLNORIGIN=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}