Gene: ARHGAP22 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4838605
rs4838605
ARHGAP22
0.810 GeneticVariation BEFREE This study confirmed that two variants (rs1073203 and rs4838605) are associated with advanced stages of DR in our cohort. 24526447

2014
dbSNP: rs4838605
rs4838605
ARHGAP22
C 0.810 GeneticVariation GWASDB Genome-wide association study of diabetic retinopathy in a Taiwanese population. 21310492

2011
dbSNP: rs4838605
rs4838605
ARHGAP22
C 0.810 GeneticVariation GWASCAT Genome-wide association study of diabetic retinopathy in a Taiwanese population. 21310492

2011
dbSNP: rs10491034
rs10491034
ARHGAP22
0.010 GeneticVariation BEFREE Two susceptibility SNPs in ARHGAP22 were found to be associated with an increased risk of DR both before and after the adjustment: rs10491034 under the dominant model (adjusted OR = 0.51, 95% CI = 0.27-0.95, p = 0.032) and additive model (adjusted OR = 0.47, 95% CI = 0.26-0.84, p = 0.0098) and rs3844492 under the codominant model (adjusted OR = 3.14, 95% CI = 1.10-9.01, p = 0.023) and recessive model (adjusted OR = 3.52, 95% CI = 1.26-9.85, p = 0.011). 28544509

2017
dbSNP: rs3844492
rs3844492
ARHGAP22
0.010 GeneticVariation BEFREE Two susceptibility SNPs in ARHGAP22 were found to be associated with an increased risk of DR both before and after the adjustment: rs10491034 under the dominant model (adjusted OR = 0.51, 95% CI = 0.27-0.95, p = 0.032) and additive model (adjusted OR = 0.47, 95% CI = 0.26-0.84, p = 0.0098) and rs3844492 under the codominant model (adjusted OR = 3.14, 95% CI = 1.10-9.01, p = 0.023) and recessive model (adjusted OR = 3.52, 95% CI = 1.26-9.85, p = 0.011). 28544509

2017