{{Rsnum
|rsid=121912973
|Chromosome=21
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CRYAA
|position=43172105
|Gene_s=CRYAA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=123580
|rsnum=121912973
|variant=0004
}}{{ClinVar
|rsid=121912973
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=44592215
|CHROM=21
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CRYAA:1409
|GENE_NAME=CRYAA
|GENE_ID=1409
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.44592215G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000018473.28; RCV000059327.21
|CLNDBN=Cataract, autosomal dominant, multiple types, with microcornea; Cataract, autosomal dominant
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=123580.0004; 123580.0007
|Disease=Cataract
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=C1858679:604219:1377:98991:98995
}}