{{Rsnum
|rsid=104893617
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CNGA3
|position=98396811
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CNGA3
}}{{omim
|id=600053
|rsnum=104893617
|variant=0006
}}{{ClinVar
|rsid=104893617
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=99013274
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=CNGA3:1261
|GENE_NAME=CNGA3
|GENE_ID=1261
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.99013274C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600053.0006
|CLNSIG=5
|CLNCUI=C0302129
|CLNDBN=Rod monochromatism
|Disease=Rod monochromatism
|CLNACC=RCV000010086.1
|Tags=PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0302129:102450007
}}