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 4676595 rs1684609 A G rs1684609 1.50E-04 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 16 4692113 rs6500627 G A rs6500627 9.13E-04 Acute lung injury HPOID:0002088 DOID:850 A intron GWASdb_trait 16 4719981 rs1659495 G A rs1659495 7.03E-05 Serum albumin level HPOID:0010876 DOID:557|DOID:409|DOID:1287 C intron GWASdb_trait 16 4721468 rs715109 T C rs715109 1.07E-05 Serum albumin level HPOID:0010876 DOID:557|DOID:409|DOID:1287 C intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000102858.12 MGRN1 607559