TABLE 1.
SNP | Nearby gene | Chr. | EA | OA | EAF | β | SE | p‐value | R 2 | F statistic |
---|---|---|---|---|---|---|---|---|---|---|
rs10182181 | ADCY3 | 2 | G | A | 0.50 | 0.057 | 0.009 | 2.10E‐10 | 0.0016 | 19.88 |
rs10853932 | KCTD15 | 19 | C | T | 0.69 | 0.067 | 0.011 | 1.30E‐09 | 0.0019 | 23.47 |
rs12444979* | GPRC5B | 16 | T | C | 0.06 | −0.079 | 0.013 | 1.80E‐09 | 0.0007 | 7.99 |
rs12623218 | TMEM18 | 2 | A | T | 0.88 | 0.110 | 0.012 | 5.80E‐22 | 0.0025 | 31.08 |
rs13130484 | GNPDA2 | 4 | T | C | 0.42 | 0.071 | 0.009 | 3.90E‐14 | 0.0025 | 30.16 |
rs1421085 | FTO | 16 | C | T | 0.45 | 0.140 | 0.009 | 5.80E‐50 | 0.0097 | 119.61 |
rs2030323 | BDNF | 11 | C | A | 0.78 | 0.079 | 0.011 | 1.10E‐12 | 0.0021 | 25.97 |
rs2206277 | TFAP2B | 6 | T | C | 0.10 | 0.080 | 0.012 | 5.60E‐12 | 0.0011 | 13.59 |
rs2568958 | NEGR1 | 1 | A | G | 0.65 | 0.062 | 0.009 | 1.10E‐11 | 0.0017 | 21.41 |
rs2596125 | HNF4G | 8 | T | C | 0.44 | −0.052 | 0.009 | 5.90E‐09 | 0.0013 | 16.32 |
rs523288 | MC4R | 18 | T | A | 0.29 | 0.099 | 0.011 | 1.70E‐20 | 0.0040 | 49.31 |
rs633715 | SEC16B | 1 | C | T | 0.27 | 0.078 | 0.011 | 4.00E‐12 | 0.0024 | 29.17 |
rs8028313 | MAP2K5 | 15 | G | C | 0.22 | −0.065 | 0.011 | 2.00E‐09 | 0.0015 | 17.74 |
rs9816226 | ETV5 | 3 | T | A | 0.85 | 0.070 | 0.012 | 2.00E‐09 | 0.0012 | 15.20 |
Abbreviations: Chr, chromosome; EA, effect allele; EAF, effect allele frequency; OA, other allele; SE, standard error; SNP, single nucleotide polymorphism.
Weak instrumental variable.