INTS12
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
4106604786rs11728044GCrs117280442.75E-09Pulmonary functionHPOID:0002795DOID:2841|DOID:3083CintronGWASdb_trait
4106606608rs11726569AGrs117265692.70E-09Pulmonary functionHPOID:0002795DOID:2841|DOID:3083AintronGWASdb_trait
4106617361rs12374256GArs123742562.80E-09Pulmonary functionHPOID:0002795DOID:2841|DOID:3083GintronGWASdb_trait
4106619140rs11727189GTrs117271895.00E-17Pulmonary functionHPOID:0002795DOID:2841|DOID:3083GintronGWASdb_trait
4106625263rs10516523GTrs105165232.22E-05Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
4106629009rs17262764GArs172627641.64E-05HypertensionHPOID:0000822DOID:10763AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000138785.14 INTS12 611355