|
CHR
|
SNP
|
Gene
|
CA
|
CAF
|
OR
|
95% CI
|
p-value
|
|---|
|
1
|
rs4846835
|
GALNT2
|
A
|
0.11
|
2.37
|
1.56–3.60
|
5.00 × 10− 5
|
|
1
|
rs34783939
|
GALNT2
|
C
|
0.15
|
2.09
|
1.44–3.02
|
8.73 × 10− 5
|
|
21
|
rs9982695
|
C21orf33
|
A
|
0.24
|
2.09
|
1.44–3.02
|
8.74 × 10− 5
|
|
4
|
rs3775202
|
VEGFC
|
G
|
0.43
|
1.92
|
1.38–2.66
|
9.70 × 10−5
|
|
2
|
rs13423742
|
FN1
|
C
|
0.06
|
3.04
|
1.73–5.36
|
1.14 × 10− 4
|
|
6
|
rs7454156
|
BMP6
|
G
|
0.18
|
2.08
|
1.42–3.02
|
1.37 × 10− 4
|
|
6
|
rs9479726
|
RGS17-OPRM1
|
A
|
0.24
|
0.41
|
0.25–0.64
|
1.54 × 10−4
|
|
19
|
rs1671152
|
GP6
|
A
|
0.32
|
1.91
|
1.36–2.68
|
1.60 × 10−4
|
|
10
|
rs286489
|
LOC101929727
|
A
|
0.28
|
1.90
|
1.35–2.66
|
1.80 × 10−4
|
|
5
|
rs4336354
|
HTR4
|
G
|
0.09
|
2.51
|
1.54–4.07
|
1.86 × 10−4
|
- Logistic regression assuming an additive genetic model was performed for 138 cases and 1376 controls adjusted by age, sex, principal components, and median diastolic blood pressure. For the ten most significant associations, chromosome (CHR), SNP ID (rs number), gene, coded allele (CA), coded allele frequency (CAF), odds ratio (OR), 95% confidence interval (CI), and p-value are given
