Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28688791
rs28688791
HDAC9
0.020 GeneticVariation BEFREE The CC genotype of rs28688791 (P = 0.037) was also associated with moderate and severe stro</span>ke (NIHSS ≥ 6). 30565168

2019
dbSNP: rs28688791
rs28688791
HDAC9
0.020 GeneticVariation BEFREE Apolipoprotein L1 (APOL1) rs73885319 (OR = 1.52; CI: 1.09-2.13, P-value = .013), rs2383207 in CDKN2A/CDKN2B (OR = 3.08; CI: 1.15-8.26, P -value = .026) and rs2107595 (OR = 1.70; CI: 1.12-2.60, P-value = .014) and rs28688791 (OR = 1.52; CI: 1.03-2.26, P-value = .036) in HDAC9 gene were associated with SVD stroke at 0.05 significance level. 28975602

2018