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 7 151043221 rs17173096 T C rs17173096 2.17E-04 Hearing function HPOID:0000365 DOID:2742 T intron GWASdb_trait 7 151062348 rs405281 G A rs405281 6.88E-04 Amyotrophic Lateral Sclerosis HPOID:0007354 DOID:332 C intron GWASdb_trait 7 151069296 rs6963048 A G rs6963048 2.45E-04 IgE levels HPOID:0010701 DOID:6024 A intron GWASdb_trait 7 151069296 rs6963048 A G rs6963048 6.55E-06 Corneal structure HPOID:0000481 DOID:10124 A intron GWASdb_trait 7 151071225 rs199876601 C T rs199876601 0.000031 Breast cancer(er negative) HPOID:0003002 DOID:1612 NA missense GWASdb_trait 7 151073747 rs202096934 G A rs202096934 0.000039 Breast cancer (ER positive) HPOID:0003002 DOID:1612 NA missense GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000013374.15 NUB1 607981