{{Rsnum
|rsid=397514587
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALG13
|position=111685059
|Gene_s=ALG13
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=X
|CLNACC=RCV000032994.7
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1s
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN160488:300884:324422
|CLNHGVS=NC_000023.10:g.110928287A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300776.0001
|Disease=Congenital disorder of glycosylation type 1s
|FwdALT=G
|FwdREF=A
|GENEINFO=ALG13:79868
|GENE_ID=79868
|GENE_NAME=ALG13
|REF=A
|RSPOS=110928287
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514587
}}