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 69830328 rs6499255 A G rs6499255 1.00E-06 IgE levels HPOID:0010701 DOID:6024 G intron GWASdb_trait 16 69950656 rs904810 T C rs904810 2.80E-04 Telomere length HPOID:0000118 NA G intron GWASdb_trait 16 69951291 rs904809 A G rs904809 4.30E-05 Bulimia nervosa HPOID:0100739 DOID:12129 T intron GWASdb_trait 16 69951291 rs904809 A G rs904809 3.26E-04 Telomere length HPOID:0000118 NA T intron GWASdb_trait 16 69970000 rs2270842 T G rs2270842 4.60E-04 Amyotrophic Lateral Sclerosis HPOID:0007354 DOID:332 G intron GWASdb_trait 16 69970329 rs1983016 A G rs1983016 2.96E-04 Amyotrophic Lateral Sclerosis HPOID:0007354 DOID:332 G cds-synon GWASdb_trait 16 69971965 rs3762177 A G rs3762177 2.36E-04 Amyotrophic Lateral Sclerosis HPOID:0007354 DOID:332 C intron GWASdb_trait 16 69974659 rs3748386 G A rs3748386 9.29E-04 Myocardial Infarction HPOID:0001658 DOID:5844 C UTR-3 GWASdb_trait 16 69975360 rs1052429 G A rs1052429 3.93E-04 Amyotrophic Lateral Sclerosis HPOID:0007354 DOID:332 A UTR-3 GWASdb_trait 16 69975360 rs1052429 G A rs1052429 1.40E-04 Bone mineral density HPOID:0004348 DOID:0080011 A UTR-3 GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000198373.12 WWP2 602308