{{Rsnum
|rsid=104893619
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CNGA3
|position=98396755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CNGA3
}}{{omim
|id=600053
|rsnum=104893619
|variant=0008
}}{{ClinVar
|rsid=104893619
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=99013218
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CNGA3:1261
|GENE_NAME=CNGA3
|GENE_ID=1261
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.99013218G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600053.0008
|CLNSIG=5
|CLNCUI=C0302129
|CLNDBN=Rod monochromatism
|Disease=Rod monochromatism
|CLNACC=RCV000010088.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0302129:102450007
}}