{{Rsnum
|rsid=118203913
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RFT1
|position=53123791
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RFT1
}}{{omim
|id=611908
|rsnum=118203913
|variant=0001
}}{{ClinVar
|rsid=118203913
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=53157807
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RFT1:91869
|GENE_NAME=RFT1
|GENE_ID=91869
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.53157807G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=611908.0001
|CLNSIG=5
|CLNCUI=C2677590
|CLNDBN=Congenital disorder of glycosylation type 1N
|Disease=Congenital disorder of glycosylation type 1N
|CLNACC=RCV000000821.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C2677590:612015:244310
}}