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[Preprint]. 2024 May 20:2024.05.20.24307608. [Version 1] doi: 10.1101/2024.05.20.24307608

Table 2.

New 35 migraine risk loci identified from the meta-analysis of 98,374 migraine cases and 869,160 controls.

Locus name RSID Chrom osome Position GRCh37 Effect allele Other allele Effect allele frequency Log-odds ratio S.e. P-value
near RUNX3 rs71014329 1 25348950 I D 0.604 0.034 0.005 2.57E-10
ST3GAL3 rs783302 1 44366341 G A 0.878 0.047 0.008 1.68E-09
SF3B4 rs7544531 1 149897217 T C 0.084 0.072 0.012 5.08E-09
near DTL rs61830764 1 212289976 A G 0.382 0.031 0.006 3.71E-08
near APLF rs112706954 2 68819969 G A 0.023 0.137 0.017 7.88E-16
TMEM131 rs2305142 2 98375722 G A 0.322 0.031 0.005 1.18E-08
near GPD2 rs74482068 2 157560108 D I 0.039 0.076 0.014 1.76E-08
near RANP7 rs11386839 3 22929430 D I 0.500 0.029 0.005 7.68E-09
ADD1 rs10026792 4 2862190 G A 0.687 0.032 0.005 2.79E-09
EPHA5 rs147908403 4 66362482 C T 0.054 0.069 0.012 2.80E-09
ITGA1 rs4865540 5 52184268 C A 0.820 0.037 0.007 1.41E-08
near GLRA1 rs372257780 5 151200938 I D 0.599 0.033 0.006 2.27E-09
KCNIP1 rs78151838 5 170108683 A G 0.905 0.054 0.010 1.82E-08
MAML1 rs10794701 5 179181061 A G 0.119 0.043 0.008 3.57E-08
near COX19 rs117303395 7 1001963 A G 0.019 0.122 0.022 4.40E-08
MAD1L1 rs10479762 7 2045351 T C 0.419 0.029 0.005 8.01E-09
ELAVL2 rs10966033 9 23705736 G T 0.617 0.029 0.005 2.70E-08
near ZCCHC7 rs10973207 9 37100525 T G 0.187 0.042 0.007 1.04E-10
near LMX1B rs4358894 9 129464802 C G 0.513 0.030 0.005 3.33E-09
near DENND5A rs34494849 11 9287030 C T 0.768 0.034 0.006 1.17E-08
near MTCH2 rs11039324 11 47665686 G A 0.601 0.030 0.005 9.76E-09
MRE11A rs639311 11 94205747 C T 0.681 0.033 0.005 9.02E-10
IPO8 rs12369125 12 30807195 A C 0.251 0.036 0.006 7.08E-10
MGAT4C rs73187675 12 86409247 T A 0.193 0.037 0.006 6.08E-09
RP11-562L8.1 rs1957110 14 29777492 T C 0.409 0.029 0.005 1.59E-08
INSM2 rs2296919 14 36005659 T C 0.807 0.038 0.006 3.44E-09
RPS6KA5 rs117151272 14 91415550 A T 0.026 0.097 0.018 3.59E-08
near ONECUT1 rs1899730 15 53166138 T G 0.707 0.032 0.006 2.11E-08
FAM174B rs12910861 15 93218540 C T 0.227 0.037 0.006 2.15E-09
FAM65A rs9934328 16 67573367 C G 0.137 0.049 0.007 1.32E-11
TUBG2 rs2292750 17 40811781 C T 0.452 0.030 0.005 3.53E-09
near NRTN rs76899991 19 5822370 G T 0.963 0.077 0.014 2.89E-08
SYMPK rs74821481 19 46320041 G T 0.678 0.036 0.005 4.59E-11
near SERHL2 rs141478056 22 42939927 G A 0.120 0.046 0.008 2.23E-08
near FTHL17 rs149675702 23 31063624 C T 0.945 0.079 0.014 4.56E-08

RSID = reference SNP ID, GRCh37 = Genome Reference Consortium Human Build 37, s.e. = standard error. Alleles D and I refer to deletion and insertion, respectively.