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 17 61712964 rs7209435 T C rs7209435 7.00E-07 Height HPOID:0000002 NA C intron GWASdb_trait 17 61716705 rs9903897 T A rs9903897 2.50E-09 Height HPOID:0000002 NA A intron GWASdb_trait 17 61724695 rs8081612 C T rs8081612 1.30E-22 Height HPOID:0000002 NA T intron GWASdb_trait 17 61724695 rs8081612 C T rs8081612 1.60E-12 Height HPOID:0000002 NA T intron GWASdb_trait 17 61724695 rs8081612 C T rs8081612 2.60E-09 Height HPOID:0000002 NA T intron GWASdb_trait 17 61724695 rs8081612 C T rs8081612 3.74E-05 Height HPOID:0000002 NA T intron GWASdb_trait 17 61728881 rs8075273 C A rs8075273 6.32E-05 Lymphocyte counts HPOID:0004332|HPOID:0002665 DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287 C intron GWASdb_trait 17 61763031 rs11658329 G C rs11658329 6.00E-10 Height HPOID:0000002 NA C intron GWASdb_trait 17 61763031 rs11658329 G C rs11658329 5.00E-10 Height HPOID:0000002 NA C intron GWASdb_trait 17 61765524 rs9901507 G A rs9901507 6.50E-05 Amyotrophic lateral sclerosis (sporadic) HPOID:0007354 DOID:332 A intron GWASdb_trait 17 61772050 rs15637 C G rs15637 1.10E-09 Height HPOID:0000002 NA C UTR-3 GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000198909.7 MAP3K3 602539