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. 2019 Jan 16;8:e39595. doi: 10.7554/eLife.39595

Table 1. Ten candidate causal variants, shared as caQTLs across all 10 populations.

GWAS information is from the GRASP database (Eicher et al., 2015). See Supplementary file 3 for all caQTL/GWAS overlaps.

Chr caQTL position caQTL rsID GWAS rsID GWAS p-value GWAS trait Candidate gene
 15 86018746 rs7161880 rs4281668 9.90E-09 Aggressive
prostate cancer
AKAP13
 9 5097544 rs3780372 rs10974944 5.10E-32 Myeloproliferative neoplasms JAK2
 12 111351439 rs11065769 rs10849917 3.21E-08 Coronary artery disease MYL2
 2 68598955 rs17035378 rs17035378 8.00E-09 Celiac disease PLEK
 6 167433948 rs6904946 rs2301436 1.00E-12 Crohn's disease RNASET2
 14 69273905 rs194749 rs194749 2.70E-10 Inflammatory bowel disease ZFP36L1
 1 154359411 rs9651053 rs11265608 2.75E-08 Juvenile idiopathic arthritis IL6R
 4 1731653 rs798764 rs798766 3.90E-13 Urinary
bladder cancer
FGFR3
 13 40334852 rs9603612 rs9532434 4.52E-08 Juvenile idiopathic arthritis COG6
 11 118560857 rs73001406 rs11216930 1.40E-09 Glioma PHLDB1