UCHL3
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1376136648rs9543976GArs95439767.00E-06Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947AintronGWASdb_trait
1376136648rs9543976GArs95439767.40E-06Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947AintronGWASdb_trait
1376138830rs2328964GTrs23289646.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947AintronGWASdb_trait
1376143572rs2296146TCrs22961467.20E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947TintronGWASdb_trait
1376162039rs7982517AGrs79825173.00E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947GintronGWASdb_trait
1376165282rs3783028TCrs37830284.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947AintronGWASdb_trait
1376167141rs7317250GArs73172504.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947GintronGWASdb_trait
1376169777rs2031236GArs20312364.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947GintronGWASdb_trait
1376170886rs6562915GTrs65629154.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947TintronGWASdb_trait
1376171222rs6562916AGrs65629164.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947GintronGWASdb_trait
1376171331rs4885322AGrs48853223.16E-05Alcohol and nictotine co-dependenceHPOID:0000707DOID:0050741|DOID:0050742GintronGWASdb_trait
1376171331rs4885322AGrs48853224.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947GintronGWASdb_trait
1376172414rs4885323CTrs48853234.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947CintronGWASdb_trait
1376172434rs9543990GC,Trs95439904.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947TintronGWASdb_trait
1376172744rs7996884TArs79968844.70E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947TintronGWASdb_trait
1376173719rs7339146GArs73391465.00E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947GintronGWASdb_trait
1376175526rs2328963CTrs23289635.10E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947GintronGWASdb_trait
1376179170rs8192763ATrs81927635.20E-07Diabetic retinopathyHPOID:0000819|HPOID:0000488DOID:8947TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000118939.17 UCHL3 603090