Table 2.
New variants identified as independent signals in the approximate conditional analysis
Single SNP meta-analysis |
Approximate conditional meta-analysis |
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Trait | Chromosome: position | rsID | Trait-raising/ other allele | %EAF | β | SE | P-value | N | β | SE | P-value | Conditioned on | Locus |
HDL | 4:102816487 | rs1163291291,4 | T/C | 99.97 | 1.835 | 0.448 | 4.23E-05 | 9023 | 1.842 | 0.448 | 3.99E-05 | rs13107325 | SLC39A8 |
11:117112526 | rs795541102,3 | T/G | 37.94 | 0.038 | 0.009 | 5.69E-05 | 24 813 | 0.034 | 0.009 | 2.16E-04 | rs2266788, rs35120633, rs186808413 | APOA1 | |
11:116707044 | rs1384071551,4 | A/T | 99.88 | 0.589 | 0.143 | 3.98E-05 | 20 910 | 0.505 | 0.143 | 4.09E-04 | rs2266788, rs35120633, rs186808413, rs79554110 | APOA1 | |
15:58830639 | rs1400297291,4 | A/G | 99.92 | 1.019 | 0.273 | 1.88E-04 | 8544 | 0.963 | 0.273 | 4.14E-04 | rs1800588, rs10468017 | LIPC | |
15:58837989 | rs2006843241,4 | A/G | 0.13 | 0.760 | 0.223 | 6.62E-04 | 7941 | 0.721 | 0.223 | 1.23E-03 | rs1800588, rs10468017, rs140029729 | LIPC | |
18:47113165 | rs1176236311,4 | T/C | 0.22 | 0.389 | 0.116 | 8.36E-04 | 17 028 | 0.390 | 0.116 | 8.08E-04 | rs77960347, rs4939883 | LIPG | |
19:45448465 | rs51671,4,5 | G/T | 36.02 | 0.042 | 0.009 | 6.19E-06 | 25 337 | 0.046 | 0.009 | 8.70E-07 | rs769449 | APOE | |
19:45028231 | rs360532771,4 | G/A | 99.62 | 0.304 | 0.079 | 1.14E-04 | 22 141 | 0.289 | 0.079 | 2.43E-04 | rs769449, rs5167 | APOE | |
LDL | 6:161018174 | rs77706283,8 | C/T | 45.47 | 0.030 | 0.009 | 1.38E-03 | 23 595 | 0.035 | 0.009 | 2.03E-04 | rs3798220 | LPA |
12:121660770 | rs1458147491,4 | G/A | 99.91 | 0.768 | 0.205 | 1.85E-04 | 13 946 | 0.768 | 0.205 | 1.85E-04 | rs34606562 | HNF1A | |
19:45448036 | rs11328991,4,5 | T/C | 47.49 | 0.033 | 0.009 | 3.37E-04 | 24 201 | 0.037 | 0.009 | 4.71E-05 | rs7412, rs769449, rs445925, rs3208856 | APOE | |
TC | 2:21229160 | rs57429041,4 | T/C | 0.05 | 1.676 | 0.260 | 2.53E-11 | 13 764 | 1.679 | 0.260 | 2.38E-11 | rs541041, rs1367117, rs533617 | APOB |
TG | 2:27550967 | rs104981711 | A/G | 59.83 | 0.053 | 0.009 | 5.42E-09 | 26 031 | −0.030a | 0.007 | 2.54E-05 | rs1260326 | GCKR |
11:116701353 | rs763532039,10 | C/T | 99.96 | 1.258 | 0.320 | 8.60E-05 | 11 860 | 1.279 | 0.320 | 6.58E-05 | rs2266788, rs35120633 | APOA1 | |
15:42436237 | rs1397889071,4 | G/A | 0.04 | 1.665 | 0.421 | 7.67E-05 | 6731 | 1.668 | 0.421 | 7.49E-05 | rs2412710 | CAPN3 | |
16:57015091 | rs58801,4 | C/G | 5.09 | 0.085 | 0.021 | 3.85E-05 | 24 330 | 0.078 | 0.021 | 1.33E-04 | rs3764261 | CETP |
Non-synonymous variant,
common variant,
intron variant,
missense variant,
nonsense-mediated mRNA decay transcript variant,
non-coding exon variant,
non-coding transcript variant,
NHGRI catalogue,
stop gained variant,
splice region variant,
synonymous rs7770628 has been previously published for LPA eQTL.
Change in the direction of the conditional effect.