{{Rsnum
|rsid=387906888
|Chromosome=1
|position=63414141
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AAT)
|geno3=(AAT;AAT)
|Gene=ALG6
|Gene_s=ALG6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000023373.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1C
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1864178:603147:ORPHA79320
|CLNHGVS=NC_000001.11:g.63414141_63414143delAAT
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_013339.3:c.897_899delAAT; 604566.0005
|Disease=Congenital disorder of glycosylation type 1C
|FwdREF=AAT
|REF=TAAT
|RSPOS=63414137
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000005000002110200
|WGT=1
|dbSNPBuildID=137
|rsid=387906888
|GENEINFO=ALG6:29929
|GENE_ID=29929
|GENE_NAME=ALG6
|CLNORIGIN=1
}}