ATG5
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
6106667535rs9372120TGrs93721204.00E-08Rheumatoid arthritisHPOID:0001370DOID:7148TintronGWASdb_trait
6106667535rs9372120TGrs93721208.00E-10Rheumatoid arthritisHPOID:0001370DOID:7148TintronGWASdb_trait
6106675819rs1769972TCrs17699721.57E-05Soluble levels of adhesion moleculesHPOID:0002597DOID:2388AintronGWASdb_trait
6106683876rs538557TCrs5385571.36E-26NarcolepsyHPOID:0100786DOID:8986TintronGWASdb_trait
6106685195rs3827644GCrs38276445.00E-07Systemic lupus erythematosus and Systemic sclerosisHPOID:0002725DOID:9074|DOID:1578GintronGWASdb_trait
6106718522rs3851210CTrs38512105.80E-04SchizophreniaHPOID:0100753DOID:5419CintronGWASdb_trait
6106727215rs3804333CTrs38043332.40E-05Systemic lupus erythematosusHPOID:0002725DOID:9074CintronGWASdb_trait
6106734040rs633724CTrs6337241.19E-04Arthritis (juvenile idiopathic)HPOID:0005681DOID:676TintronGWASdb_trait
6106734040rs633724CTrs6337244.40E-04Systemic lupus erythematosusHPOID:0002725DOID:9074TintronGWASdb_trait
6106749308rs12212740GArs122127405.08E-04Alzheimer's diseaseHPOID:0002511DOID:10652GintronGWASdb_trait
6106764866rs573775GArs5737751.36E-07Systemic lupus erythematosusHPOID:0002725DOID:9074TintronGWASdb_trait
6106772773rs3804338CTrs38043382.10E-04Type 2 diabetesHPOID:0005978DOID:9352CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000057663.13 ATG5 604261