{{Rsnum
|rsid=387906550
|Chromosome=1
|position=196673968
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CFH
|Gene_s=CFH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=1
|CLNACC=RCV000018030.26
|CLNALLE=1
|CLNDBN=Basal laminar drusen
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0730295:126700:ORPHA75376:312926005
|CLNHGVS=NC_000001.11:g.196673968T>G
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000186.3:c.350+6T>G; 134370.0021
|Disease=Basal laminar drusen
|FwdALT=G
|FwdREF=T
|REF=T
|RSPOS=196673968
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;INT;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060080005000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387906550
|GENEINFO=CFH:3075
|GENE_ID=3075
|GENE_NAME=CFH
|CLNORIGIN=1
}}