Disease associated variation - GWASdb Chr Pos SNP ID(dbSNP 142) Ref Alt Ori SNP ID P-value Drug Name Drug Anno GWAS Trait HPO ID DO ID AA Type Trait or Drug 4 40064563 rs7674515 C T rs7674515 3.22E-05 CHOLESTEROL CHOLESTEROL, LDL|APOLIPOPROTEIN C-III|TRIGLYCERIDES|CHOLESTEROL, HDL|LIPIDS|DIETARY FATS Triglycerides HPOID:0003119 DOID:3393|DOID:3146|DOID:2349 C intron GWASdb_drug 4 40064563 rs7674515 C T rs7674515 3.22E-05 Triglycerides HPOID:0003119 DOID:3393|DOID:3146|DOID:2349 C intron GWASdb_trait 4 40064563 rs7674515 C T rs7674515 3.22E-05 Polyunsaturated fatty acid levels, in plasma HPOID:0011022|HPOID:0000716|HPOID:0001626|HPOID:0000819|HPOID:0000726 DOID:9351|DOID:1287|DOID:1307|DOID:1596 C intron GWASdb_trait 4 40064563 rs7674515 C T rs7674515 1.92E-05 Basophils HPOID:0001912 DOID:74|DOID:114 C intron GWASdb_trait 4 40071926 rs17439873 T C rs17439873 3.44E-04 Multiple complex diseases HPOID:0000118 NA T intron GWASdb_trait 4 40074742 rs1706023 G A rs1706023 8.77E-04 Rheumatoid arthritis HPOID:0001370 DOID:7148 C intron GWASdb_trait 4 40120420 rs17619330 C T rs17619330 2.79E-08 Lymphocyte counts HPOID:0004332|HPOID:0002665 DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287 C intron GWASdb_trait 4 40121562 rs794001 G A rs794001 2.84E-04 Type 2 diabetes HPOID:0005978 DOID:9352 A missense GWASdb_trait 4 40139719 rs794009 T G rs794009 2.10E-04 Amyotrophic lateral sclerosis (sporadic) HPOID:0007354 DOID:332 C intron GWASdb_trait 4 40140338 rs794008 C T rs794008 3.83E-04 Type 2 diabetes HPOID:0005978 DOID:9352 A intron GWASdb_trait 4 40159617 rs7656730 T C rs7656730 0.00000104 Platelet thrombus as measured by PFA-100ColA closure time upon shear stress NA NA T UTR-3 GWASdb_trait