Table 4.
SNP | CHR | Tested allele |
MAF | Effect direction |
OR | SE | Discovery p |
I2 |
---|---|---|---|---|---|---|---|---|
rs173539 | 16 | T | 0.31 | +++ | 1.25 | 0.06 | 6.00×10−4 | 0 |
-- rs247617 (r2=0.99) | 16 | A | 0.31 | +++ | 1.24 | 0.06 | 8.74×10−4 | 0 |
-- rs17231506 (r2=0.99) | 16 | T | 0.31 | +++ | 1.23 | 0.06 | 9.13×10−4 | 0 |
-- rs711752 (r2=0.62) | 16 | A | 0.42 | ++− | 1.15 | 0.06 | 2.08×10−2 | 14 |
-- rs708272 (r2=0.61) | 16 | A | 0.42 | ++− | 1.15 | 0.06 | 2.23×10−2 | 18 |
Association results for rs173539 in association with ICH risk, as well as four additional SNPs in linkage disequilibrium (LD) with rs173539 chosen for replication. CHR = chromosome, MAF = minor allele frequency, OR = odds ratio, SE = standard error, r2 = degree of LD with rs173539. SNP = single nucleotide polymorphism, + = variant increases ICH risk, − = variant decreases ICH risk.