{{Rsnum
|rsid=121907921
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=PAX6
|position=31801893
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAX6
}}{{omim
|id=607108
|rsnum=121907921
|variant=0015
}}{{ClinVar
|rsid=121907921
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=31823441
|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.31823441A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607108.0015
|CLNSIG=5
|CLNCUI=C0344559; C1858679
|CLNDBN=Irido-corneo-trabecular dysgenesis; Foveal hypoplasia; Foveal hypoplasia with anterior segment anomalies
|Disease=Irido-corneo-trabecular dysgenesis; Foveal hypoplasia; Foveal hypoplasia with anterior segment anomalies
|CLNACC=RCV000003638.2; RCV000003640.2; RCV000003641.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=C0344559:604229:708:204153003; C2673946; C1850994
}}