Skip to main content
. Author manuscript; available in PMC: 2019 May 1.
Published in final edited form as: Circ Genom Precis Med. 2018 May;11(5):e002037. doi: 10.1161/CIRCGEN.117.002037

Table 2.

Common variants significantly associated with PR interval from meta-analysis of all studies

SNP Locus Closest gene Function Coding allele CAF* Beta SE P value Number of studies Prolong or shorten PR interval Novel locus
rs6795970 3p22.2 SCN10A Missense A 0.37 0.1705 0.0052 4.0×10−240 27 Prolong
rs3922844 3p22.2 SCN5A Intronic A 0.34 −0.1069 0.0053 9.3×10−90 26 Shorten
rs3807989 7q31.2 CAV1 Intronic A 0.43 0.0908 0.0050 3.0×10−74 27 Prolong
rs7660702 4q21.23 ARHGAP24 Intronic C 0.33 −0.0921 0.0053 1.2×10−68 27 Shorten
rs17287293 12p12.1 LINC00477 Intergenic G 0.14 −0.1084 0.0071 1.9×10−52 27 Shorten
rs11897119 2p14 MEIS1 Intronic C 0.39 0.0566 0.0055 4.2×10−25 25 Prolong
rs1896312 12q24.21 TBX3 Intergenic G 0.28 0.0564 0.0055 8.7×10−25 26 Prolong
rs883079 12q24.21 TBX5 3′UTR G 0.29 0.0550 0.0054 4.5×10−24 26 Prolong
rs116202356 3p22.2 DLEC1 Missense A 0.02 −0.1953 0.0199 1.0×10−22 27 Shorten
rs251253 5q35.1 CREBRF Intergenic G 0.42 −0.0439 0.0051 4.7×10−18 26 Shorten
rs11153730 6q22.31 SLC35F1 Intergenic C 0.47 −0.0420 0.0049 9.5×10−18 27 Shorten Novel
rs35658696 5q21.1 PAM Missense G 0.04 0.0956 0.0119 8.5×10−16 27 Prolong
rs2070492 3p22.2 SLC22A14 Missense T 0.10 0.0624 0.0083 4.0×10−14 27 Prolong Novel
rs2585897 13q12.11 XPO4 Intronic A 0.17 0.0471 0.0064 2.8×10−13 27 Prolong
rs2042995 2q31.2 TTN Missense C 0.26 0.0375 0.0057 4.3×10−11 27 Prolong
rs4399693 2p25.1 ID2 Intergenic A 0.34 0.0374 0.0058 9.1×10−11 25 Prolong
rs41306688 13q34 ADPRHL1 Missense C 0.03 0.1002 0.0173 7.4×10−9 22 Prolong Novel
rs4745 1q22 EFNA1 Missense T 0.49 0.0299 0.0053 1.2×10−8 26 Prolong
rs11078078 17p12 LINC00670 Intronic A 0.40 0.0281 0.0050 2.2×10−8 27 Prolong
rs60632610 10q22.2 SYNPO2L Missense T 0.15 −0.0371 0.0068 4.5×10−8 27 Shorten Novel
rs11848785 14q24.2 SIPA1L1 Intronic G 0.24 0.0317 0.0058 4.6×10−8 27 Prolong
rs3733414 4q35.2 FAT1 Missense A 0.38 0.0280 0.0051 4.8×10−8 27 Prolong
rs17362588 2q31.2 CCDC141 Missense A 0.08 −0.0491 0.0090 5.5×10−8 27 Shorten Novel
rs2296172 1p34.3 MACF1 Missense G 0.20 0.0326 0.0061 1.1×10−7 27 Prolong Novel
rs9398652 6q22.31 GJA1 Intergenic A 0.14 0.0390 0.0074 1.3×10−7 26 Prolong Novel
rs442177 4q22.1 AFF1 Intronic C 0.42 −0.0262 0.0050 1.8×10−7 26 Shorten Novel
rs7002002 8q24.3 PLEC Missense A 0.38 −0.0272 0.0052 2.1×10−7 25 Shorten Novel
rs1768208 3p22.1 MOBP Intron T 0.25 0.0288 0.0057 3.6×10−7 27 Prolong Novel
rs2119788 4q34.1 HAND2 Intergenic C 0.52 −0.0246 0.0049 5.6×10−7 27 Shorten Novel
rs17391905 1p32.3 C1orf185 Intergenic G 0.03 −0.0694 0.0142 9.6×10−7 27 Shorten
rs524295 10q24.1 ALDH18A1 Intergenic A 0.40 −0.0261 0.0053 9.7×10−7 26 Shorten
*

Coding allele frequency

SNP was not significant if African participants were excluded.

Some variants did not reach pass the quality filtering in respective studies and thus were excluded.