Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 17101 single nucleotide variant NM_001002255.1(SUMO4):c.163G>A (p.Val55Met) 237025 MedGen:C1838260,OMIM:600320 6 149721690 149721690 G A 17101 single nucleotide variant NM_001002255.1(SUMO4):c.163G>A (p.Val55Met) 237025 MedGen:C1838260,OMIM:600320 6 149400554 149400554 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 6 149721690 rs237025 G A rs237025 9.56E-05 Serum metabolites HPOID:0011111 NA C missense GWASdb_trait 6 149721690 rs237025 G A rs237025 3.63E-04 Suicide attempts in bipolar disorder HPOID:0007302 DOID:3312 C missense GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000177688.6 SUMO4 608829