Gene: RPGRIP1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853124
rs137853124
RPGRIP1
A 0.700 CausalMutation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019
dbSNP: rs1057518122
rs1057518122
RPGRIP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555303320
rs1555303320
RPGRIP1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs28937883
rs28937883
RPGRIP1
T 0.700 CausalMutation CLINVAR

dbSNP: rs398124354
rs398124354
RPGRIP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs574462207
rs574462207
RPGRIP1
G 0.700 CausalMutation CLINVAR

dbSNP: rs61751266
rs61751266
RPGRIP1
G 0.700 CausalMutation CLINVAR

dbSNP: rs759940113
rs759940113
RPGRIP1
T 0.700 CausalMutation CLINVAR

dbSNP: rs776880045
rs776880045
RPGRIP1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs780667159
rs780667159
RPGRIP1
T 0.700 GeneticVariation CLINVAR