Table 3.
Lead SNP | CHR | Tested allele |
MAF | Effect direction |
OR | SE | Discovery p |
I2 |
---|---|---|---|---|---|---|---|---|
rs173539 | 16 | T | 0.31 | +++ | 1.25 | 0.06 | 6.00E-4 | 0 |
rs820299 | 16 | G | 0.38 | − − − | 0.81 | 0.06 | 7.50E-4 | 48 |
rs158478 | 16 | A | 0.48 | +++ | 1.21 | 0.06 | 1.48E-3 | 56 |
CHR = chromosome, MAF = minor allele frequency, OR = odds ratio, SE = standard error, SNP = single nucleotide polymorphism, + = variant increases ICH risk, − = variant decreases ICH risk.