GNB1L
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
2219785006rs2269726TCrs22697269.88E-05Erythrocyte countsHPOID:0001627|HPOID:0001871DOID:74|DOID:114CintronGWASdb_trait
2219787736rs748806CTrs7488062.98E-20Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287AintronGWASdb_trait
2219792619rs5993833AGrs59938334.90E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
2219792712rs5993834TCrs59938344.87E-04Lung function (forced expiratory volume in 1 second to forced vital capacity ratio)HPOID:0002088DOID:850CintronGWASdb_trait
2219817433rs9306226TCrs93062269.50E-05Attention deficit hyperactivity disorderHPOID:0007018DOID:1094TintronGWASdb_trait
2219825223rs7287254ACrs72872547.48E-05Lung function (forced expiratory volume in 1 second)HPOID:0002088DOID:850CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000185838.13 GNB1L 610778