{{Rsnum
|rsid=121909210
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TGFBI
|position=136046406
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TGFBI
}}{{omim
|id=601692
|rsnum=121909210
|variant=0003
}}{{ClinVar
|rsid=121909210
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=135382095
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TGFBI:7045
|GENE_NAME=TGFBI
|GENE_ID=7045
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000005.9:g.135382095C>A; NC_000005.9:g.135382095C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601692.0008; 601692.0003
|CLNSIG=5
|CLNCUI=C1690006
|CLNDBN=CORNEAL DYSTROPHY, GROENOUW TYPE I; Lattice corneal dystrophy Type I
|Disease=CORNEAL DYSTROPHY; Lattice corneal dystrophy Type I
|CLNACC=RCV000008322.1; RCV000008317.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1690006:122200:98964:419197009
}}