{{Rsnum
|rsid=137853200
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=EPHA2
|position=16129440
|Gene_s=EPHA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=176946
|variant=0002
|rsnum=137853200
}}{{ClinVar
|rsid=137853200
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=16129440
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=EPHA2:1969
|GENE_NAME=EPHA2
|GENE_ID=1969
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.16129440G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004431.3:c.2819C>T; 176946.0002
|CLNSIG=5
|CLNCUI=C1861825
|CLNDBN=Cataract 6
|Disease=Cataract 6
|CLNACC=RCV000014169.17
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=C1861825:116600:613020:ORPHA91492:ORPHA98993:ORPHA98994
}}