Promoter region SNP position SNP ID Gene Disease Type P-value Source
chr20:34359896-34538292 chr20:34383634 rs11906854 PHF20 Migraine - clinic-based intron 7e-06 GWASdb
chr20:34359896-34538292 chr20:34384646 rs17430100 PHF20 Protein C levels intron 3.92e-45 GWASdb
chr20:34359896-34538292 chr20:34390527 rs6060612 PHF20 Common traits (Other) intron 6.31e-10 GWASdb
chr20:34359896-34538292 chr20:34429931 rs17345771 PHF20 Protein C levels intron 5.28e-45 GWASdb
chr20:34359896-34538292 chr20:34440380 rs2425168 PHF20 Protein C levels intron 5.87e-45 GWASdb
chr20:34359896-34538292 chr20:34445142 rs2425173 PHF20 Protein C levels intron 2.72e-08 GWASdb
chr20:34359896-34538292 chr20:34445375 rs2425174 PHF20 Protein C levels intron 6.16e-45 GWASdb
chr20:34359896-34538292 chr20:34448810 rs2064511 PHF20 Protein C levels intron 2.75e-08 GWASdb
chr20:34359896-34538292 chr20:34458599 rs6060649 PHF20 Protein C levels intron 9.56e-45 GWASdb
chr20:34359896-34538292 chr20:34460479 rs6058339 PHF20 Melanoma intron 1.69e-07 GWASdb
chr20:34359896-34538292 chr20:34470012 rs6060658 PHF20 Protein C levels intron 3.03e-44 GWASdb
chr20:34359896-34538292 chr20:34489565 rs7267005 PHF20 Narcolepsy intron 6.1e-32 GWASdb
chr20:34359896-34538292 chr20:34509678 rs6060684 PHF20 Protein C levels intron 3.62e-44 GWASdb
chr20:34359896-34538292 chr20:34513655 rs6121089 PHF20 Protein C levels intron 3.66e-44 GWASdb
chr20:34359896-34538292 chr20:34515490 rs6058368 PHF20 Protein C levels intron 3.67e-44 GWASdb
chr20:34359896-34538292 chr20:34517135 rs6060690 PHF20 Protein C levels intron 6.84e-45 GWASdb
chr20:34359896-34538292 chr20:34529734 rs6060702 PHF20 Multiple complex diseases intron 0.000353 GWASdb