USP13
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
3179385000rs6443664CTrs64436641.99E-05Calcium levelsHPOID:0004363|HPOID:0002621|HPOID:0011915DOID:10575|DOID:1936TintronGWASdb_trait
3179388406rs4854942CTrs48549427.88E-04Type 2 diabetesHPOID:0005978DOID:9352CintronGWASdb_trait
3179390043rs12636924TCrs126369245.20E-06Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
3179391320rs4854945TGrs48549458.38E-05Non-alcoholic fatty liver disease histology (other)HPOID:0001397|HPOID:0006561DOID:9452TintronGWASdb_trait
3179394123rs4855104TGrs48551048.76E-05Non-alcoholic fatty liver disease histology (other)HPOID:0001397|HPOID:0006561DOID:9452TintronGWASdb_trait
3179399946rs6807974AGrs68079742.22E-12Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287AintronGWASdb_trait
3179404673rs9816744CTrs98167446.26E-04Smoking quantityHPOID:0000707DOID:0050742CintronGWASdb_trait
3179408054rs61760203CTrs617602030.0000663Nonsyndromic striae distensae (stretch marks)HPOID:0001000DOID:37CmissenseGWASdb_trait
3179425147rs2284887AGrs22848872.52E-05Mammographic densityHPOID:0000769DOID:0050671CintronGWASdb_trait
3179425959rs2268939AGrs22689393.30E-05Mammographic densityHPOID:0000769DOID:0050671CintronGWASdb_trait
3179436298rs4854951CTrs48549519.98E-05Non-alcoholic fatty liver disease histology (other)HPOID:0001397|HPOID:0006561DOID:9452CintronGWASdb_trait
3179438464rs116049736CTrs1160497360.00000573Nonsyndromic striae distensae (stretch marks)HPOID:0001000DOID:37CintronGWASdb_trait
3179448869rs2268937CGrs22689378.47E-05Mammographic densityHPOID:0000769DOID:0050671CintronGWASdb_trait
3179455796rs17195948GArs171959481.02E-06Vascular dementiaHPOID:0000726DOID:8725GintronGWASdb_trait
3179474767rs3732992AGrs37329925.13E-04Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
3179482482rs1024852TCrs10248526.91E-06Vascular dementiaHPOID:0000726DOID:8725GintronGWASdb_trait
3179495657rs13327135AGrs133271351.07E-04Smoking initiationHPOID:0000707DOID:0050742AintronGWASdb_trait
3179498965rs759596CArs7595967.90E-05Smoking initiationHPOID:0000707DOID:0050742TintronGWASdb_trait
3179499215rs17195983GTrs171959832.59E-04Smoking initiationHPOID:0000707DOID:0050742GintronGWASdb_trait
3179499960rs12107867GArs121078675.32E-04Smoking initiationHPOID:0000707DOID:0050742A,GintronGWASdb_trait
3179500901rs16848333ACrs168483332.89E-05Smoking initiationHPOID:0000707DOID:0050742AintronGWASdb_trait
3179504309rs9814513CTrs98145132.23E-04Smoking initiationHPOID:0000707DOID:0050742TUTR-3GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000058056.8 USP13 603591