PPP2R2C
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
46345038rs7441490GArs74414909.69E-04GEMCITABINE|CYTARABINEMANNOSYLTRANSFERASES|PIGB PROTEIN, HUMAN|RNA, SMALL INTERFERING|DEOXYCYTIDINEResponse to cytadine analogues (cytosine arabinoside)HPOID:0002664DOID:162AintronGWASdb_drug
46412401rs10008136AGrs100081360.000853METHIONINECASPASE 1|CASPASE 9|CASP9 PROTEIN, HUMAN|5'-METHYLTHIOADENOSINE|APIP PROTEIN, HUMAN|DEOXYADENOSINES|THIONUCLEOSIDES|APOPTOSIS REGULATORY PROTEINSSalmonella-induced pyroptosisNANAAintronGWASdb_drug
46342213rs4689408CTrs46894081.50E-05HypertensionHPOID:0000822DOID:10763CintronGWASdb_trait
46345038rs7441490GArs74414909.69E-04Response to cytadine analogues (cytosine arabinoside)HPOID:0002664DOID:162AintronGWASdb_trait
46348191rs6856061TCrs68560613.76E-05Coronary heart diseaseHPOID:0001677DOID:3393TintronGWASdb_trait
46352060rs11727760AGrs117277609.80E-05HIV-1 controlHPOID:0002721DOID:526AintronGWASdb_trait
46367467rs6831971TCrs68319717.66E-05Adverse response to chemotherapy (neutropenia/leucopenia) (all platinum-based drugs)HPOID:0001875|HPOID:0001882DOID:1227TintronGWASdb_trait
46369384rs4272078TCrs42720784.91E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
46381323rs4327561GArs43275618.43E-05BasophilsHPOID:0001912DOID:74|DOID:114AintronGWASdb_trait
46384823rs6851340CTrs68513401.80E-05HypothyroidismHPOID:0000821DOID:1459CintronGWASdb_trait
46400507rs4689433GTrs46894338.00E-06Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
46400860rs5019274TCrs50192741.30E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
46412401rs10008136AGrs100081360.000853Salmonella-induced pyroptosisNANAAintronGWASdb_trait
46417785rs16838780TCrs168387800.000199fMRI brain tests in schizophreniaHPOID:0100753DOID:5419TintronGWASdb_trait
46465438rs13129773GArs131297737.40E-04Amyotrophic Lateral SclerosisHPOID:0007354DOID:332GintronGWASdb_trait
46465791rs7664714TCrs76647141.40E-05Fasting plasma glucoseHPOID:0003162DOID:9352CintronGWASdb_trait
46517005rs4571410CTrs45714103.09E-05Glycosylated haemoglobin levelsHPOID:0011902|HPOID:0000077|HPOID:0001626|HPOID:0000819|HPOID:0000479DOID:1287|DOID:9351|DOID:557|DOID:5679GintronGWASdb_trait
46517066rs4565150TCrs45651503.69E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
46552201rs4302525CTrs43025252.64E-04Alzheimer's disease (late onset)HPOID:0002511DOID:10652CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000074211.13 PPP2R2C 605997