{{Rsnum
|rsid=74315435
|Gene=VSX1
|Chromosome=20
|position=25077727
|Orientation=minus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=VSX1
}}{{omim
|id=605020
|rsnum=74315435
|variant=0004
}}{{ClinVar
|rsid=74315435
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=25058363
|CHROM=20
|GMAF=0.0014
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=VSX1:30813
|GENE_NAME=VSX1
|GENE_ID=30813
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.25058363C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605020.0004
|CLNSIG=5
|CLNCUI=C1857964
|CLNDBN=Craniofacial anomalies and anterior segment dysgenesis syndrome
|Disease=Craniofacial anomalies and anterior segment dysgenesis syndrome
|CLNACC=RCV000005562.1
|Tags=RV;PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1857964:614195
|COMMON=1
}}