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 19 45769575 rs2240672 G A rs2240672 6.36E-04 Alzheimer's disease HPOID:0002511 DOID:10652 A intron GWASdb_trait 19 45779635 rs345409 T C rs345409 6.52E-04 Alzheimer's disease HPOID:0002511 DOID:10652 C intron GWASdb_trait 19 45801951 rs11672894 C T rs11672894 0.0000016 Common carotid artery thickness (far walls) HPOID:0000822|HPOID:0001627|HPOID:0001297|HPOID:0000077|HPOID:0011420 DOID:3407 C intron GWASdb_trait 19 45801951 rs11672894 C T rs11672894 0.0000028 Common carotid artery thickness (average of near and far wall measures) HPOID:0000822|HPOID:0001627|HPOID:0001297|HPOID:0000077|HPOID:0011420 DOID:3407 C intron GWASdb_trait 19 45808142 rs344797 T G rs344797 9.22E-04 Alcohol dependence HPOID:0000707 DOID:0050741 G UTR-3 GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000007047.14 MARK4 606495