{{Rsnum
|rsid=121913061
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CFH
|position=196690125
|Gene_s=CFH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134370
|rsnum=121913061
|variant=0019
}}{{ClinVar
|rsid=121913061
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=196690125
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=CFH:3075
|GENE_NAME=CFH
|GENE_ID=3075
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.196690125C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000186.3:c.1222C>T; 134370.0019
|CLNSIG=5
|CLNCUI=C0730295
|CLNDBN=Basal laminar drusen
|Disease=Basal laminar drusen
|CLNACC=RCV000018028.22
|Tags=PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0730295:126700:ORPHA75376:312926005
}}