{{Rsnum
|rsid=121912543
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VSX2
|position=74259621
|Gene_s=VSX2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=142993
|rsnum=121912543
|variant=0001
}}{{ClinVar
|rsid=121912543
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=74726324
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=VSX2:338917
|GENE_NAME=VSX2
|GENE_ID=338917
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000014.8:g.74726324G>A; NC_000014.8:g.74726324G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000015985.24; RCV000015986.24; RCV000015987.24
|CLNDBN=Microphthalmia, cataracts, and iris abnormalities; Microphthalmia, isolated 2
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet
|CLNDSDBID=C1864722; C1864720:610093:2542
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142993.0001; 142993.0002
|Disease=Microphthalmia
}}