{{Rsnum
|rsid=74315433
|Gene=VSX1
|Chromosome=20
|position=25079460
|Orientation=minus
|GMAF=0.005051
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=VSX1
}}{{omim
|id=605020
|rsnum=74315433
|variant=0002
}}{{ClinVar
|rsid=74315433
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=25060096
|CHROM=20
|GMAF=0.005
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=VSX1:30813
|GENE_NAME=VSX1
|GENE_ID=30813
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000020.10:g.25060096C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605020.0002
|CLNSIG=5
|CLNCUI=C0339284; C1835677
|CLNDBN=Polymorphous corneal dystrophy; Keratoconus 1
|Disease=Polymorphous corneal dystrophy; Keratoconus 1
|CLNACC=RCV000005560.1; RCV000024251.1
|Tags=RV;PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9949; 0.005051; .
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM
|CLNDSDBID=C0339284:122000:98973:29504002; C1835677:148300
|COMMON=1
}}