{{Rsnum
|rsid=121918204
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RPGRIP1L
|position=53652637
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RPGRIP1L
}}{{omim
|id=610937
|rsnum=121918204
|variant=0009
}}{{ClinVar
|rsid=121918204
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=53686549
|CHROM=16
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RPGRIP1L:23322
|GENE_NAME=RPGRIP1L
|GENE_ID=23322
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.53686549G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610937.0009
|CLNSIG=5
|CLNCUI=C1969053
|CLNDBN=Joubert syndrome 7
|Disease=Joubert syndrome 7
|CLNACC=RCV000001131.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1325:C1969053:611560:220497
}}