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. 2023 Aug 7;94(4):713–726. doi: 10.1002/ana.26743

TABLE 3.

Summary of the Genomic Loci Associated with Cluster Headache in Trans‐Ancestry GWAS

Locus name Lead variant (Chr:Pos) EA/NEA (EAF) χ 2 (df) p association p ancestry Variant type
DUSP10 rs12129860 (1:222153461) G/T (0.196) 90.86 (4) 8.64 × 10−19 9.59 × 10−3 Regulatory region
CAPN2 rs10916600 (1:223897012) T/C (0.214) 66.43 (4) 1.28 × 10−13 1.80 × 10−11 Intron
MERTK rs10188642 (2:112741099) A/G (0.521) 182.48 (4) 2.19 × 10−38 0.40 Intron
FTCDNL1 rs4673382 (2:200492346) G/A (0.653) 164.96 (4) 1.26 × 10−34 0.52 Intergenic
FHL5 rs11153085 (6:97066355) T/A (0.326) 88.53 (4) 2.70 × 10−18 0.30 Regulatory region
PLCE1 rs2274224 (10:96039597) G/C (0.551) 58.68 (4) 5.48 × 10−12 0.28 Missense variant
LRP1 rs11172113 (12:57527283) T/C (0.635) 46.08 (4) 2.37 × 10−9 0.40 Intron

Note: Locus name = the closest protein‐coding gene within a 250‐Kb window.

Abbreviation: χ 2 = chi square test statistic from MR‐MEGA; Ancestry = heterogeneity due to different ancestry; Chr = chromosome; df = number degrees of freedom; EA = effect allele, which here is set to correspond with the risk allele; EAF = effect allele frequency; NEA = non‐effect allele; Pos = position (hg19).