Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137854466
rs137854466
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs142285818
rs142285818
RHO
G 0.700 CausalMutation CLINVAR

dbSNP: rs1423415130
rs1423415130
XYLT2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555976049
rs1555976049
NDP ; NDP-AS1
CTTCA 0.700 GeneticVariation CLINVAR

dbSNP: rs397515804
rs397515804
FBN1
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358284
rs80358284
FZD4 ; PRSS23
C 0.700 CausalMutation CLINVAR

dbSNP: rs1042522
rs1042522
TP53
0.010 GeneticVariation BEFREE The C allele for rs1042522 in p53 was genetically associated with a higher risk for RD but not for PVR in this cohort. 28106707

2018
dbSNP: rs2229094
rs2229094
LTA ; LOC100287329
0.010 GeneticVariation BEFREE No significant differences in the allelic distributions of the previously identified risk C allele for LTA rs2229094 were observed between RD subjects and controls (odds ratio [95% confidence interval] = 0.8 [0.5-1.2]; P = 0.3). 28106707

2018
dbSNP: rs372029024
rs372029024
COL1A1
0.010 GeneticVariation BEFREE In the patient diagnosed with PCG and retinal detachment, analysis of WES data identified compound heterozygous variants in COL1A1 (p.Met264Leu; p.Ala1083Thr). 27484908

2016
dbSNP: rs2279744
rs2279744
MDM2
0.010 GeneticVariation BEFREE Results indicate that the G allele of rs2279744 is associated with a higher risk of developing PVR in patients undergoing a RD surgery. 24349246

2013