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 13 111781060 rs12853515 C G rs12853515 2.00E-06 Homeostasis model assessment of insulin resistance (interaction) HPOID:0005978 DOID:9352 C intron GWASdb_trait 13 111781060 rs12853515 C G rs12853515 4.00E-06 Fasting insulin (interaction) HPOID:0008283 DOID:9352 C intron GWASdb_trait 13 111782877 rs831159 A T rs831159 5.69E-04 Obesity (extreme) HPOID:0001513 DOID:9970 T intron GWASdb_trait 13 111795544 rs831167 C T rs831167 8.40E-06 Bilirubin levels HPOID:0002904 DOID:2741 C intron GWASdb_trait 13 111797920 rs831169 G A rs831169 9.00E-06 Bilirubin levels HPOID:0002904 DOID:2741 G intron GWASdb_trait 13 111817665 rs1891958 A G rs1891958 8.30E-06 Bilirubin levels HPOID:0002904 DOID:2741 C intron GWASdb_trait 13 111818832 rs4773330 A G rs4773330 8.00E-06 Bilirubin levels HPOID:0002904 DOID:2741 G intron GWASdb_trait 13 111821289 rs9301494 G C rs9301494 7.80E-06 Bilirubin levels HPOID:0002904 DOID:2741 C intron GWASdb_trait 13 111834095 rs7987430 G C rs7987430 7.00E-06 Urinary metabolites HPOID:0000079 DOID:557 G intron GWASdb_trait 13 111854193 rs1164270 C T rs1164270 7.90E-06 Urinary metabolites HPOID:0000079 DOID:557 A intron GWASdb_trait 13 111867501 rs2147686 C A rs2147686 5.03E-05 Parent of origin effect on language impairment (maternal) HPOID:0002463 DOID:93 T intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000102606.17 ARHGEF7 605477