SH3RF2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5145316958rs17104037TCrs171040373.63E-04GEMCITABINE|CYTARABINEMANNOSYLTRANSFERASES|PIGB PROTEIN, HUMAN|RNA, SMALL INTERFERING|DEOXYCYTIDINEResponse to cytidine analogues (gemcitabine)HPOID:0002664DOID:162TintronGWASdb_drug
5145316958rs17104037TCrs171040373.63E-04Response to cytidine analogues (gemcitabine)HPOID:0002664DOID:162TintronGWASdb_trait
5145380097rs2400207AGrs24002073.00E-05Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
5145386138rs1859894TGrs18598941.50E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
5145387254rs758038GCrs7580382.80E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
5145409070rs11743632GArs117436324.47E-04Coronary Artery DiseaseHPOID:0001677DOID:3393AintronGWASdb_trait
5145418274rs7706656AGrs77066568.21E-04Coronary Artery DiseaseHPOID:0001677DOID:3393GintronGWASdb_trait
5145425583rs2962522CTrs29625229.26E-04Coronary Artery DiseaseHPOID:0001677DOID:3393CintronGWASdb_trait
5145426248rs9325002TCrs93250027.00E-05Type 2 diabetesHPOID:0005978DOID:9352TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000156463.17 SH3RF2 613377