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 14 103862322 rs2010281 G A rs2010281 1.80E-09 Bone mineral density (spine) HPOID:0004348 DOID:0080011 A intron GWASdb_trait 14 103879187 rs2065018 T C rs2065018 3.68E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 14 103883633 rs11623869 G T rs11623869 5.00E-16 Bone mineral density HPOID:0004348 DOID:0080011 G intron GWASdb_trait 14 103901424 rs12894275 G A rs12894275 2.22E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 14 103901424 rs12894275 G A rs12894275 3.74E-05 Height HPOID:0000002 NA G intron GWASdb_trait 14 103904061 rs2065015 T G rs2065015 2.36E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 14 103947289 rs3783397 A G rs3783397 2.94E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 14 103949378 rs3783398 T C rs3783398 3.11E-04 Multiple complex diseases HPOID:0000118 NA T intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000075413.17 MARK3 602678