{{Rsnum
|rsid = 28939087
|Gene = SLC35C1
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=11
|position=45806240
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC35C1
}}{{omim
|desc=CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc
|id=605881
|rsnum=28939087
|variant=0001
}}

{{ClinVar
|rsid=28939087
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=45827791
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SLC35C1:55343
|GENE_NAME=SLC35C1
|GENE_ID=55343
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.45827791C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605881.0001
|CLNSIG=5
|CLNCUI=C0796132
|CLNDBN=Congenital disorder of glycosylation type 2C
|Disease=Congenital disorder of glycosylation type 2C
|CLNACC=RCV000005005.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1332:C0796132:266265:2968:99843
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}