{{Rsnum
|rsid = 28937883
|Gene = RPGRIP1
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=14
|position=21325943
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RPGRIP1
}}{{omim
|desc=CONE-ROD DYSTROPHY 9
|id=605446
|rsnum=28937883
|variant=0005
}}

{{ClinVar
|rsid=28937883
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=21794102
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=RPGRIP1:57096
|GENE_NAME=RPGRIP1
|GENE_ID=57096
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.21794102G>T
|CLNSRC=GeneReviews; OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=NBK1298; 605446.0005; RISN-RPGRIP:c.2480G>T
|CLNSIG=5
|CLNCUI=C2750720
|CLNDBN=Cone-rod dystrophy 13; not provided
|Disease=Cone-rod dystrophy 13; not provided
|CLNACC=RCV000005274.2; RCV000086245.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1298:C2750720:608194:1872
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}