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 79540449 rs7405450 C T rs7405450 5.45E-04 Amyotrophic Lateral Sclerosis HPOID:0007354 DOID:332 T intron GWASdb_trait 17 79541116 rs9911383 G A rs9911383 8.68E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 17 79558976 rs8075102 T G rs8075102 8.18E-04 Parkinson's disease HPOID:0001300 DOID:14330 G intron GWASdb_trait 17 79560494 rs1122424 C T rs1122424 4.68E-04 Multiple complex diseases HPOID:0000118 NA T intron GWASdb_trait 17 79574124 rs11652797 G A rs11652797 1.80E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 17 79585492 rs75078292 A G rs75078292 0.00000098 Myopia (Age of onset) HPOID:0000545 DOID:11830 NA intron GWASdb_trait 17 79596811 rs9894429 C T rs9894429 9.00E-14 Eye color HPOID:0000478 DOID:240 C cds-synon GWASdb_trait 17 79602820 rs6565612 T C rs6565612 2.71E-04 Multiple complex diseases HPOID:0000118 NA T intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000182446.13 NPLOC4 606590