{{Rsnum
|rsid=121909050
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HSF4
|position=67165742
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HSF4
}}{{omim
|id=602438
|rsnum=121909050
|variant=0004
}}{{ClinVar
|rsid=121909050
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=67199645
|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.67199645A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602438.0004
|CLNSIG=5
|CLNCUI=C0266537
|CLNDBN=Cataract, zonular
|Disease=Cataract
|CLNACC=RCV000007512.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0266537:116800:98995
}}