{{Rsnum
|rsid=121908281
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RAX2
|position=3770767
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAX2
}}{{omim
|id=610362
|rsnum=121908281
|variant=0002
}}{{ClinVar
|rsid=121908281
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=3770765
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RAX2:84839
|GENE_NAME=RAX2
|GENE_ID=84839
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.3770765C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610362.0002
|CLNSIG=5
|CLNCUI=C1835865
|CLNDBN=Cone-rod dystrophy 11
|Disease=Cone-rod dystrophy 11
|CLNACC=RCV000001300.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1835865:610381:1872
}}