TNIP1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5150425467rs2233299GArs22332992.10E-04ALANINE|PROLINETNIP1 PROTEIN, HUMAN|HLA-B8 ANTIGEN|DNA-BINDING PROTEINSMyasthenia gravisHPOID:0001290DOID:437Ccds-synonGWASdb_drug
5150432446rs17111695TCrs171116955.70E-05METHAMPHETAMINENAMethamphetamine dependenceHPOID:0000707DOID:670TintronGWASdb_drug
5150438988rs1422673CTrs14226736.20E-09ALANINE|PROLINETNIP1 PROTEIN, HUMAN|HLA-B8 ANTIGEN|DNA-BINDING PROTEINSMyasthenia gravisHPOID:0001290DOID:437TintronGWASdb_drug
5150440097rs2233287GArs22332874.60E-09ALANINE|PROLINETNIP1 PROTEIN, HUMAN|HLA-B8 ANTIGEN|DNA-BINDING PROTEINSMyasthenia gravisHPOID:0001290DOID:437CintronGWASdb_drug
5150450236rs4958881TCrs49588813.00E-10ALANINE|PROLINETNIP1 PROTEIN, HUMAN|HLA-B8 ANTIGEN|DNA-BINDING PROTEINSMyasthenia gravisHPOID:0001290DOID:437CintronGWASdb_drug
5150451650rs3792785TCrs37927853.60E-08ALANINE|PROLINETNIP1 PROTEIN, HUMAN|HLA-B8 ANTIGEN|DNA-BINDING PROTEINSMyasthenia gravisHPOID:0001290DOID:437AintronGWASdb_drug
5150455732rs3792783AGrs37927831.70E-08ALANINE|PROLINETNIP1 PROTEIN, HUMAN|HLA-B8 ANTIGEN|DNA-BINDING PROTEINSMyasthenia gravisHPOID:0001290DOID:437CintronGWASdb_drug
5150462638rs13168551TCrs131685516.00E-06ALANINE|PROLINETNIP1 PROTEIN, HUMAN|HLA-B8 ANTIGEN|DNA-BINDING PROTEINSMyasthenia gravisHPOID:0001290DOID:437CintronGWASdb_drug
4164069949rs2320615AGrs23206153.30E-04Telomere lengthHPOID:0000118NACintronGWASdb_trait
4164076558rs1351222GArs13512224.52E-04Telomere lengthHPOID:0000118NATintronGWASdb_trait
5150409477rs2277940TCrs22779401.27E-07SchizophreniaHPOID:0100753DOID:5419TnearGene-3GWASdb_trait
5150425467rs2233299GArs22332992.10E-04Myasthenia gravisHPOID:0001290DOID:437Ccds-synonGWASdb_trait
5150431030rs888989CTrs8889892.74E-05Multiple sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:2377TintronGWASdb_trait
5150432153rs2112635CTrs21126350.000425AsthmaHPOID:0002099DOID:2841TintronGWASdb_trait
5150432446rs17111695TCrs171116956.55E-05Type 2 diabetesHPOID:0005978DOID:9352TintronGWASdb_trait
5150432446rs17111695TCrs171116955.70E-05Methamphetamine dependenceHPOID:0000707DOID:670TintronGWASdb_trait
5150434894rs6579837GTrs65798370.00000171Rheumatoid arthritis (CCP positive)HPOID:0001370DOID:7148GintronGWASdb_trait
5150434894rs6579837GTrs65798370.0000404Rheumatoid arthritisHPOID:0001370DOID:7148GintronGWASdb_trait
5150435480rs3805433CGrs38054330.00047Endometrial cancerHPOID:0012114DOID:1380GintronGWASdb_trait
5150438988rs1422673CTrs14226730.000000272AsthmaHPOID:0002099DOID:2841TintronGWASdb_trait
5150438988rs1422673CTrs14226736.20E-09Myasthenia gravisHPOID:0001290DOID:437TintronGWASdb_trait
5150438988rs1422673CTrs14226731.78E-05AsthmaHPOID:0002099DOID:2841TintronGWASdb_trait
5150440097rs2233287GArs22332875.00E-09Systemic sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0000362|HPOID:0006918|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:418CintronGWASdb_trait
5150440097rs2233287GArs22332870.0000865AsthmaHPOID:0002099DOID:2841CintronGWASdb_trait
5150440097rs2233287GArs22332874.60E-09Myasthenia gravisHPOID:0001290DOID:437CintronGWASdb_trait
5150440097rs2233287GArs22332875.83E-05AsthmaHPOID:0002099DOID:2841CintronGWASdb_trait
5150441761rs147561136TCrs1475611360.000069Prostate cancer (advanced)HPOID:0012125DOID:10283TmissenseGWASdb_trait
5150446316rs4562032CArs45620320.0000044Mean arterial pressureHPOID:0001677DOID:3393CintronGWASdb_trait
5150450236rs4958881TCrs49588811.19E-05Systemic sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0000362|HPOID:0006918|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:418CintronGWASdb_trait
5150450236rs4958881TCrs49588810.000158AsthmaHPOID:0002099DOID:2841CintronGWASdb_trait
5150450236rs4958881TCrs49588813.00E-10Myasthenia gravisHPOID:0001290DOID:437CintronGWASdb_trait
5150451650rs3792785TCrs37927850.0000611AsthmaHPOID:0002099DOID:2841AintronGWASdb_trait
5150451650rs3792785TCrs37927853.60E-08Myasthenia gravisHPOID:0001290DOID:437AintronGWASdb_trait
5150451650rs3792785TCrs37927856.18E-05AsthmaHPOID:0002099DOID:2841AintronGWASdb_trait
5150455732rs3792783AGrs37927831.14E-05Systemic sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0000362|HPOID:0006918|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:418CintronGWASdb_trait
5150455732rs3792783AGrs37927830.0000526AsthmaHPOID:0002099DOID:2841CintronGWASdb_trait
5150455732rs3792783AGrs37927831.70E-08Myasthenia gravisHPOID:0001290DOID:437CintronGWASdb_trait
5150457485rs7708392GCrs77083923.80E-13Multiple sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:2377CintronGWASdb_trait
5150458146rs10036748CTrs100367482.00E-09Systemic lupus erythematosusHPOID:0002725DOID:9074TintronGWASdb_trait
5150458146rs10036748CTrs100367480.00000114AsthmaHPOID:0002099DOID:2841TintronGWASdb_trait
5150458146rs10036748CTrs100367483.00E-06Systemic lupus erythematosusHPOID:0002725DOID:9074TintronGWASdb_trait
5150458146rs10036748CTrs100367483.44E-05AsthmaHPOID:0002099DOID:2841TintronGWASdb_trait
5150461049rs960709AGrs9607092.00E-08Systemic lupus erythematosus and Systemic sclerosisHPOID:0002725DOID:9074|DOID:1578GintronGWASdb_trait
5150462638rs13168551TCrs131685510.000551AsthmaHPOID:0002099DOID:2841CintronGWASdb_trait
5150462638rs13168551TCrs131685516.00E-06Myasthenia gravisHPOID:0001290DOID:437CintronGWASdb_trait
5150462638rs13168551TCrs131685514.00E-06Systemic lupus erythematosusHPOID:0002725DOID:9074CintronGWASdb_trait
5150467189rs2233278GCrs22332782.20E-42PsoriasisHPOID:0003765DOID:8893CUTR-5GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000145901.14 TNIP1 607714