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 33365835 rs12940238 T C rs12940238 1.55E-04 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 17 33383030 rs1634800 C T rs1634800 3.94E-04 Tourette syndrome HPOID:0000709 DOID:11119|DOID:10933|DOID:1094 G intron GWASdb_trait 17 33414758 rs797989 C A rs797989 1.08E-04 Tourette syndrome HPOID:0000709 DOID:11119|DOID:10933|DOID:1094 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000092871.16 RFFL 609735