{{Rsnum
|rsid=121907920
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PAX6
|position=31801727
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAX6
}}{{omim
|id=607108
|rsnum=121907920
|variant=0014
}}{{ClinVar
|rsid=121907920
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=31823275
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PAX6:5080
|GENE_NAME=PAX6
|GENE_ID=5080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.31823275C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607108.0014
|CLNSIG=5
|CLNCUI=C1850992
|CLNDBN=Foveal hypoplasia and presenile cataract syndrome
|Disease=Foveal hypoplasia and presenile cataract syndrome
|CLNACC=RCV000003637.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1850992:136520:2253
}}