Gene: PCARE ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606691
rs267606691
PCARE
A 0.710 CausalMutation CLINVAR

dbSNP: rs863223344
rs863223344
PCARE
A 0.700 CausalMutation CLINVAR Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa. 26497376

2015
dbSNP: rs367658438
rs367658438
PCARE
T 0.700 CausalMutation CLINVAR Novel C2orf71 mutations account for ∼1% of cases in a large French arRP cohort. 21412943

2011
dbSNP: rs527236055
rs527236055
PCARE
T 0.700 GeneticVariation CLINVAR

dbSNP: rs527236056
rs527236056
PCARE
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs794728002
rs794728002
PCARE
G 0.700 CausalMutation CLINVAR