Rsid Chr Position P value Ref Alt Gwas trait Gene symbol Variant type PMID
rs2701858 chr13 41138389 0.0009 C T Atrial fibrillation FOXO1 intron 21846873
rs2701859 chr13 41141232 0.000651 T C Myopia (pathological) FOXO1 intron 21095009
rs9549236 chr13 41147158 0.000625 T C Multiple complex diseases FOXO1 intron 17554300
rs2951787 chr13 41161770 0.000001 G A Urinary metabolites FOXO1 intron 21572414
rs4943794 chr13 41173408 0.00028 G C Longevity and age-related phenotypes FOXO1 intron 17903295
rs7986407 chr13 41179798 0.000635 A G Myopia (pathological) FOXO1 intron 21095009
rs10507486 chr13 41186501 0.00013 G A Longevity and age-related phenotypes FOXO1 intron 17903295
rs9549244 chr13 41218685 0.00000944 G A Rheumatoid arthritis FOXO1 intron 19503088
rs9549244 chr13 41218685 0.000701 G A Myopia (pathological) FOXO1 intron 21095009