Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 137408 single nucleotide variant NM_001706.4(BCL6):c.143C>T (p.Thr48Met) 200263685 MedGen:CN169374 3 187451339 187451339 G A 137408 single nucleotide variant NM_001706.4(BCL6):c.143C>T (p.Thr48Met) 200263685 MedGen:CN169374 3 187733551 187733551 G A

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 3 187447032 rs1056932 G A rs1056932 3.66E-04 Suicide attempts in bipolar disorder HPOID:0007302 DOID:3312 C cds-synon GWASdb_trait 3 187448997 rs6762932 G A rs6762932 9.63E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 3 187451701 rs1880100 T C rs1880100 7.04E-04 Suicide attempts in bipolar disorder HPOID:0007302 DOID:3312 A intron GWASdb_trait 3 187454731 rs3774304 C G rs3774304 8.30E-04 Suicide attempts in bipolar disorder HPOID:0007302 DOID:3312 G intron GWASdb_trait 3 187456709 rs3733017 T G rs3733017 6.00E-06 PR interval HPOID:0012248|HPOID:0005165 DOID:10273 A intron GWASdb_trait 3 187459088 rs3172469 T G rs3172469 3.38E-04 Amyotrophic Lateral Sclerosis HPOID:0007354 DOID:332 A intron GWASdb_trait 3 187459497 rs1523474 T C rs1523474 5.36E-04 Suicide attempts in bipolar disorder HPOID:0007302 DOID:3312 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000113916.17 BCL6 109565