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.