Table 2.
Chr | Basepair position (kb) | SNP | Correlation with index SNPa | Function/gene | Coded/non-coded allele | Allele frequency | Effective sample | Effect estimate | SE | Two-sided P | Two-sided Pmeta-gc |
---|---|---|---|---|---|---|---|---|---|---|---|
6q22 | 122 187 | rs9398652 | – | Intergenic, 400 kb from GJA1 | A/C | 0.10 | 37 050 | −12.6 | 1.56 | 7.7 × 10−16 | 3.8 × 10−15 |
6q22 | 121 790 | rs11154022 | 0.006 | Intergenic, 8 kb from GJA1 | A/G | 0.33 | 31 676 | 5.8 | 1.05 | 3.5 × 10−8 | 7.2 × 10−8 |
14q12 | 22 935 | rs452036 | – | Intronic MYH6 | A/G | 0.36 | 34 640 | −7.8 | 1.00 | 8.1 × 10−15 | 3.8 × 10−14 |
14q12 | 22 931 | rs365990 | 0.96 | Non-synonymous coding MYH6 (Ala-1101-Val) | G/A | 0.37 | 32 627 | −7.7 | 1.02 | 5.4 × 10−14 | 2.1 × 10−13 |
14q12 | 23 046 | rs223116 | 0.08 | Intergenic, nearest to MYH7, NDNG | A/G | 0.24 | 26 899 | −7.4 | 1.30 | 1.1 × 10−8 | 2.5 × 10−8 |
12p12 | 24 662 | rs17287293 | – | Intergenic | G/A | 0.15 | 37 988 | 8.6 | 1.31 | 5.7 × 10−11 | 1.6 × 10−10 |
6q22 | 118 680 | rs281868 | – | Intronic SLC35F1 | G/A | 0.50 | 32 109 | −6.3 | 0.99 | 1.5 × 10−10 | 4.3 × 10−10 |
7q22 | 100 291 | rs314370 | – | Intronic SLC12A9 | C/T | 0.19 | 35 170 | −7.6 | 1.21 | 2.3 × 10−10 | 6.1 × 10−10 |
7q22 | 100 324 | rs12666989 | 0.88 | Non-synonymous coding UfSp1 (Leu-41-Val) | C/T | 0.18 | 35 750 | −7.0 | 1.21 | 9.4 × 10−9 | 2.1 × 10−8 |
11q12 | 61 327 | rs174547 | – | Intronic FADS1 | C/T | 0.33 | 34 907 | −6.2 | 1.01 | 8.2 × 10−10 | 2.1 × 10−9 |
1q32 | 206 195 | rs2745967 | – | Intergenic near CD34 | G/A | 0.37 | 34 913 | 5.4 | 0.98 | 3.2 × 10−8 | 6.6 × 10−8 |
Chromosomal positions and coded alleles are given relative to the forward strand of NCBI build 36. Effect sizes (on the millisecond scale) are shown as beta estimates from linear regression models for each additional copy of the coded allele. The effective sample size reflects the imputation quality-adjusted sample size. Final column shows the P-value from inverse variance weighted meta-analyses. Chr, chromosome; SE, standard error. Bold values indicate P < 5 × 10−8
aCEU HapMap population linkage disequilibrium r2 values to the index SNP.