{{Rsnum
|rsid=121908449
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RGS9
|position=65197160
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RGS9
}}{{omim
|id=604067
|rsnum=121908449
|variant=0001
}}{{ClinVar
|rsid=121908449
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=63193278
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RGS9:8787
|GENE_NAME=RGS9
|GENE_ID=8787
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.63193278T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604067.0001
|CLNSIG=5
|CLNCUI=C1842073
|CLNDBN=Prolonged electroretinal response suppression
|Disease=Prolonged electroretinal response suppression
|CLNACC=RCV000006220.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1842073:608415:75374
}}