{{Rsnum
|rsid=132630258
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CFP
|position=47627564
|Gene_s=CFP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300383
|variant=0001
|rsnum=132630258
}}{{ClinVar
|rsid=132630258
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=47486963
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CFP:5199
|GENE_NAME=CFP
|GENE_ID=5199
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.47486963G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300383.0001
|CLNSIG=5
|CLNCUI=C1839454
|CLNDBN=Properdin deficiency, X-linked
|Disease=Properdin deficiency
|CLNACC=RCV000011931.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1839454:312060
}}