{{Rsnum
|rsid=387906243
|Chromosome=16
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=RPGRIP1L
|position=53648999
|Gene_s=RPGRIP1L
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNACC=RCV000001132.1
|CLNALLE=1
|CLNDBN=Joubert syndrome 7
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1325:C1969053:611560:220497
|CLNHGVS=NC_000016.9:g.53682911delT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610937.0010
|Disease=Joubert syndrome 7
|FwdREF=A
|REF=GT
|RSPOS=53682910
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906243
|GENEINFO=RPGRIP1L:23322
|GENE_ID=23322
|GENE_NAME=RPGRIP1L
}}