{{Rsnum
|rsid=132630261
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CFP
|position=47626062
|Gene_s=CFP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300383
|variant=0005
|rsnum=132630261
}}{{ClinVar
|rsid=132630261
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=47485461
|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.47485461A>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000011935.1
|CLNDBN=PROPERDIN DEFICIENCY, TYPE III
|CLNDSDB=MedGen
|CLNDSDBID=C1839456
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300383.0005
|Disease=PROPERDIN DEFICIENCY
}}