{{Rsnum
|rsid=151173406
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALG1
|position=5078842
|Gene_s=ALG1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000023496.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1K
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1837896:608540:79327
|CLNHGVS=NC_000016.9:g.5128843C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605907.0007
|Disease=Congenital disorder of glycosylation type 1K
|FwdALT=T
|FwdREF=C
|GENEINFO=ALG1:56052
|GENE_ID=56052
|GENE_NAME=ALG1
|REF=C
|RSPOS=5128843
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=151173406
}}