{{Rsnum
|rsid=387907030
|Chromosome=9
|position=128946082
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=DOLK
|Gene_s=DOLK,NUP188
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=9
|CLNACC=RCV000023835.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1M
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1835849:610768:91131
|CLNHGVS=NC_000009.11:g.131708361G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610746.0003
|Disease=Congenital disorder of glycosylation type 1M
|FwdALT=G
|FwdREF=C
|REF=G
|RSPOS=131708361
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907030
|GENEINFO=DOLK:22845; NUP188:23511
|GENE_ID=22845; 23511
|GENE_NAME=DOLK; NUP188
}}