{{Rsnum
|rsid = 28935480
|Gene = CFP
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=X
|position=47626820
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFP
}}{{omim
|desc=PROPERDIN DEFICIENCY, TYPE I
|id=300383
|rsnum=28935480
|variant=0003
}}

{{ClinVar
|rsid=28935480
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=47486219
|CHROM=X
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=CFP:5199
|GENE_NAME=CFP
|GENE_ID=5199
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.47486219C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300383.0003
|CLNSIG=5
|CLNCUI=C1839454
|CLNDBN=Properdin deficiency, X-linked
|Disease=Properdin deficiency
|CLNACC=RCV000011933.16
|Tags=RV;PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1839454:312060
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}