Table 3.
Chr | SNP | Effect allele / Referent allele | EAF | Gene | Location | Beta | s.e. | P | Selected prior trait associations |
---|---|---|---|---|---|---|---|---|---|
2 | rs142556838 | C/T | 0.91 | CCDC141 | Intron | 0.306 | 0.055 | 2.30E-08 | Heart rate27 |
6 | 6:122113614 | CT/C | 0.90 | GJA1 | 0.378 | 0.052 | 3.30E-13 | Cardiac conduction29 | |
7 | rs221789 | C/T | 0.15 | GNB2 | 5' utr | -0.246 | 0.043 | 4.80E-09 | Familial sinus node and atrioventricular conduction dysfunction30,33 |
7 | rs1997571 | A/G | 0.41 | CAV1 | Intron | -0.197 | 0.032 | 5.60E-10 | Insulin resistance, metabolic syndrome32 |
12 | rs4963772 | A/G | 0.85 | BCAT1 | Intergenic | -0.244 | 0.044 | 2.20E-08 | Heart rate variability28 |
14 | rs422068 | T/C | 0.64 | MYH6 | Intron | 0.205 | 0.033 | 1.70E-10 | Familial cardiomyopathy, rare variant also associated with sick sinus syndrome31,42 |
20 | rs6127466 | G/A | 0.53 | KIAA1755 | Intron | -0.197 | 0.031 | 2.50E-10 | Heart rate27 |
21 | rs2846867 | C/T | 0.98 | C21orf37 | Intergenic | 0.181 | 0.031 | 7.40E-09 |
BCAT1 = branched chain amino acid transaminase 1; CAV1 = caveolin-1; CCDC141 = coiled-coil domain containing 141; Chr = chromosome; EAF = estimated allele frequency; GJA1 = gap junction protein alpha 1; GNB2 = G protein subunit beta 2; MYH6 = myosin heavy chain 6; s.e. = standard error; SNP = single nucleotide polymorphism.