{{Rsnum
|rsid=119469015
|Chromosome=21
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FTCD
|position=46150129
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FTCD
}}{{omim
|id=606806
|rsnum=119469015
|variant=0002
}}{{ClinVar
|rsid=119469015
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=47570043
|CHROM=21
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FTCD:10841
|GENE_NAME=FTCD
|GENE_ID=10841
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.47570043C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606806.0002
|CLNSIG=5
|CLNCUI=C0268609
|CLNDBN=Glutamate formiminotransferase deficiency
|Disease=Glutamate formiminotransferase deficiency
|CLNACC=RCV000004233.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268609:229100:51208:59761008
}}