WRNIP1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
62776303rs160699TCrs1606996.86E-05FibrinogenHPOID:0011898DOID:1287TintronGWASdb_trait
62781800rs17135709GTrs171357099.01E-04Type 2 diabetesHPOID:0005978DOID:9352TintronGWASdb_trait
62783304rs4083550AGrs40835501.38E-04Lung function (forced expiratory volume in 1 second to forced vital capacity ratio)HPOID:0002088DOID:850TintronGWASdb_trait
62784353rs160704CGrs1607049.75E-04Coronary Artery DiseaseHPOID:0001677DOID:3393CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000124535.15 WRNIP1 608196