{{Rsnum
|rsid=121909048
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HSF4
|position=67165827
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HSF4
}}{{omim
|id=602438
|rsnum=121909048
|variant=0001
}}{{ClinVar
|rsid=121909048
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=67199730
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HSF4:3299
|GENE_NAME=HSF4
|GENE_ID=3299
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.67199730T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602438.0001
|CLNSIG=5
|CLNCUI=C0266537
|CLNDBN=Cataract, zonular
|Disease=Cataract
|CLNACC=RCV000007509.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0266537:116800:98995
}}