CTTN
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1170272042rs12801756AGrs128017564.29E-04StrokeHPOID:0001297DOID:6713NAintronGWASdb_trait
1170276818rs1198236CTrs11982365.04E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000085733.15 CTTN 164765