{{Rsnum
|rsid=132630259
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CFP
|position=47628207
|Gene_s=CFP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300383
|variant=0002
|rsnum=132630259
}}{{ClinVar
|rsid=132630259
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=47487606
|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.47487606G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000011932.16
|CLNDBN=PROPERDIN DEFICIENCY, TYPE II
|CLNDSDB=MedGen
|CLNDSDBID=C1839455
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300383.0002
|Disease=PROPERDIN DEFICIENCY
}}