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 9 136676014 rs7021663 T C rs7021663 3.00E-06 IMMUNOGLOBULIN G GLYCOSYLTRANSFERASES IgG glycosylation HPOID:0010701 DOID:2531|DOID:417 C intron GWASdb_drug 9 136679080 rs756777 A G rs756777 1.00E-06 IMMUNOGLOBULIN G GLYCOSYLTRANSFERASES IgG glycosylation HPOID:0010701 DOID:2531|DOID:417 A intron GWASdb_drug 9 136723520 rs12344583 A G rs12344583 8.00E-06 FACTOR VIII SCARA5 PROTEIN, MOUSE|EPITHELIAL SODIUM CHANNELS|VON WILLEBRAND FACTOR|STAB2 PROTEIN, HUMAN|RECEPTORS, CELL SURFACE|LECTINS, C-TYPE|SYNTAXIN 1|STX2 PROTEIN, HUMAN|CELL ADHESION MOLECULES|DEGENERIN SODIUM CHANNELS|ASIC2 PROTEIN, HUMAN|SCAVENGER RECEPTORS, CLASS A|ACID SENSING ION CHANNELS|R-SNARE PROTEINS|CLEC4M PROTEIN, HUMAN|CELL ADHESION MOLECULES, NEURONAL|NERVE TISSUE PROTEINS|STXBP5 PROTEIN, HUMAN vWF and FVIII levels HPOID:0012146|HPOID:0003125|HPOID:0004936 DOID:12531|DOID:12134|DOID:866 G,A intron GWASdb_drug 9 136626906 rs642193 C A rs642193 1.63E-05 Myopia (severe) HPOID:0000545 DOID:11830 A nearGene-3 GWASdb_trait 9 136632662 rs622035 A C rs622035 8.78E-04 Parkinson's disease HPOID:0001300 DOID:14330 A intron GWASdb_trait 9 136641713 rs669443 C T rs669443 4.00E-05 Adiposity HPOID:0001513 DOID:9970 G intron GWASdb_trait 9 136643994 rs602990 T C rs602990 1.00E-04 Information processing speed HPOID:0100753|HPOID:0000716 DOID:1561 C missense GWASdb_trait 9 136658816 rs2073888 T C rs2073888 0.0000736 Normoxic and mild-hypoxic adaptation in populations residing at low and moderate altitudes HPOID:0002795 DOID:2841|DOID:3083 T intron GWASdb_trait 9 136658987 rs10993803 C T rs10993803 0.0000736 Normoxic and mild-hypoxic adaptation in populations residing at low and moderate altitudes HPOID:0002795 DOID:2841|DOID:3083 T intron GWASdb_trait 9 136676014 rs7021663 T C rs7021663 3.00E-06 IgG glycosylation HPOID:0010701 DOID:2531|DOID:417 C intron GWASdb_trait 9 136679080 rs756777 A G rs756777 1.00E-06 IgG glycosylation HPOID:0010701 DOID:2531|DOID:417 A intron GWASdb_trait 9 136723520 rs12344583 A G rs12344583 8.00E-06 vWF and FVIII levels HPOID:0012146|HPOID:0003125|HPOID:0004936 DOID:12531|DOID:12134|DOID:866 G,A intron GWASdb_trait 9 136745163 rs12115818 G A rs12115818 6.56E-05 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 9 136754076 rs2073883 C T rs2073883 4.90E-06 Urinary metabolites HPOID:0000079 DOID:557 C intron GWASdb_trait 9 136759046 rs2810545 A C rs2810545 1.44E-05 Age-related macular degeneration HPOID:0007868 DOID:10871 C intron GWASdb_trait 9 136767301 rs2157834 A C rs2157834 1.00E-04 Information processing speed HPOID:0100753|HPOID:0000716 DOID:1561 C intron GWASdb_trait 9 136767346 rs2157835 G T rs2157835 1.00E-04 Information processing speed HPOID:0100753|HPOID:0000716 DOID:1561 T intron GWASdb_trait 9 136790282 rs2265520 T C rs2265520 3.81E-04 Fibrinogen HPOID:0011898 DOID:1287 T intron GWASdb_trait 9 136797140 rs2519818 G A rs2519818 9.96E-06 Type 2 diabetes HPOID:0005978 DOID:9352 T intron GWASdb_trait 9 136802291 rs2519808 A T rs2519808 4.48E-04 Aortic root size HPOID:0002597 DOID:1287 A intron GWASdb_trait 9 136816065 rs3780786 C G rs3780786 1.23E-24 Narcolepsy HPOID:0100786 DOID:8986 C intron GWASdb_trait 9 136835343 rs3780792 A G rs3780792 1.00E-06 Multiple sclerosis HPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634 DOID:2377 A intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000160293.16 VAV2 600428