{{Rsnum
|rsid=28931604
|Gene=CRYGC
|Chromosome=2
|position=208128226
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.0004591
|Gene_s=CRYGC,ZNF224
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 98.3 | 1.7 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=CATARACT, CONGENITAL LAMELLAR
|id=123680
|rsnum=28931604
|variant=0003
}}

{{ClinVar
|rsid=28931604
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=208992950
|CHROM=2
|GMAF=0.0005
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000416110100
|GENEINFO=CRYGC:1420; LOC100507443:100507443
|GENE_NAME=CRYGC; LOC100507443
|GENE_ID=1420; 100507443
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.208992950G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000018454.24
|CLNDBN=Cataract, coppock-like
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=C1852438:604307:98984:98986:98995
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=123680.0003
|COMMON=0
|Disease=Cataract
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}