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 16 75269124 rs16957552 T C rs16957552 1.38E-08 LDL cholesterol HPOID:0010979 DOID:1936|DOID:3393 T missense GWASdb_trait 16 75269124 rs16957552 T C rs16957552 1.95E-08 Cholesterol, total HPOID:0003107 DOID:3393|DOID:3146|DOID:2349 T missense GWASdb_trait 16 75269124 rs16957552 T C rs16957552 5.13E-09 Triglycerides HPOID:0003119 DOID:3393|DOID:3146|DOID:2349 T missense GWASdb_trait 16 75275231 rs36097424 G A rs36097424 1.64E-04 Alzheimer's disease (late onset) HPOID:0002511 DOID:10652 G intron GWASdb_trait 16 75278795 rs1035540 A G rs1035540 0.00000062 Amygdala reactivity HPOID:0007302|HPOID:0100753 DOID:150 G intron GWASdb_trait 16 75281964 rs1862737 A C rs1862737 7.50E-05 Cognitive performance HPOID:0100543 DOID:1561 A UTR-5 GWASdb_trait 16 75292120 rs4888367 G A rs4888367 2.40E-05 Alzheimer's disease (late onset) HPOID:0002511 DOID:10652 A intron GWASdb_trait 16 75294211 rs4261573 T C rs4261573 1.77E-04 Multiple complex diseases HPOID:0000118 NA T,C intron GWASdb_trait 16 75295639 rs13337397 C A rs13337397 6.65E-06 Pancreatic cancer HPOID:0006725 DOID:1793 C intron GWASdb_trait 16 75296247 rs8052310 G A rs8052310 4.48E-04 Alzheimer's disease (late onset) HPOID:0002511 DOID:10652 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000050820.16 BCAR1 602941