{{Rsnum
|rsid=3213758
|Gene=RPGRIP1L
|Chromosome=16
|position=53605526
|Orientation=plus
|GMAF=0.101
|Gene_s=RPGRIP1L
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 88.5 | 11.5 | 0.0
| HCB | 53.3 | 40.1 | 6.6
| JPT | 54.0 | 39.8 | 6.2
| YRI | 100.0 | 0.0 | 0.0
| ASW | 94.7 | 5.3 | 0.0
| CHB | 53.3 | 40.1 | 6.6
| CHD | 51.4 | 41.3 | 7.3
| GIH | 85.1 | 13.9 | 1.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 91.4 | 6.9 | 1.7
| MKK | 96.8 | 3.2 | 0.0
| TSI | 88.2 | 11.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23678272
  |Trait=Vitiligo (non-segmental)
  |Title=Three new single nucleotide polymorphisms identified by a genome-wide association study in Korean patients with vitiligo.
  |RiskAllele=A
  |Pval=6E-11
  |OR=2.77
  |ORtxt=[2.04-3.76]
  |OA=1
}}

{{PMID Auto
|PMID=18565097
|Title=RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders.
|OA=1
}}

{{PMID Auto
|PMID=19430481
|Title=A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}