{{Rsnum
|rsid=121917775
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VIM
|position=17229873
|Gene_s=VIM
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=193060
|rsnum=121917775
|variant=0001
}}{{ClinVar
|rsid=121917775
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=17271872
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=VIM:7431
|GENE_NAME=VIM
|GENE_ID=7431
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.17271872G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000012983.22; RCV000056967.1
|CLNDBN=Cataract, nuclear diffuse nonprogressive; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1861827:116300:98984
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNSRCID=VIM:c.451G>A; 193060.0001
|Disease=Cataract; not provided
}}