{{Rsnum
|rsid=137853110
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=DOLK
|position=128945982
|Gene_s=DOLK,NUP188
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=610746
|variant=0002
|rsnum=137853110
}}{{ClinVar
|rsid=137853110
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=131708261
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=DOLK:22845; NUP188:23511
|GENE_NAME=DOLK; NUP188
|GENE_ID=22845; 23511
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.131708261T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610746.0002
|CLNSIG=5
|CLNCUI=C1835849
|CLNDBN=Congenital disorder of glycosylation type 1M
|Disease=Congenital disorder of glycosylation type 1M
|CLNACC=RCV000001191.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1835849:610768:91131
}}