rs886039911, RPGRIP1

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pendular Nystagmus
CUI: C0271388
Disease: Pendular Nystagmus
0.700 GeneticVariation CLINVAR
obsolete Rod-cone dystrophy
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
0.700 GeneticVariation CLINVAR
LEBER CONGENITAL AMAUROSIS 6 (disorder)
CUI: C1854260
Disease: LEBER CONGENITAL AMAUROSIS 6 (disorder)
0.700 GeneticVariation CLINVAR