{{Rsnum
|rsid=121909599
|Chromosome=4
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CNGA1
|position=47949894
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CNGA1,LOC101927157
}}{{omim
|id=123825
|rsnum=121909599
|variant=0001
}}{{ClinVar
|rsid=121909599
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=47951911
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CNGA1:1259
|GENE_NAME=CNGA1
|GENE_ID=1259
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.47951911C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=123825.0001
|CLNSIG=5
|CLNCUI=C3151059
|CLNDBN=Retinitis pigmentosa 49
|Disease=Retinitis pigmentosa 49
|CLNACC=RCV000018438.22
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3151059:613756:791
}}