TTC3
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
2138459725rs2835583AGrs28355834.43E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
2138460890rs3819262GTrs38192636.13E-04Amyotrophic Lateral SclerosisHPOID:0007354DOID:332TintronGWASdb_trait
2138460890rs67875417GGGGG,GTTrs38192636.13E-04Amyotrophic Lateral SclerosisHPOID:0007354DOID:332TintronGWASdb_trait
2138466937rs2835599GTrs28355992.19E-04Urinary albumin excretion rate in type 1 diabetesHPOID:0000079|HPOID:0100651DOID:9744GintronGWASdb_trait
2138477330rs2032088GArs20320886.13E-04Amyotrophic Lateral SclerosisHPOID:0007354DOID:332AintronGWASdb_trait
2138477330rs2032088GArs20320886.26E-09Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287AintronGWASdb_trait
2138491095rs1003719AGrs10037192.00E-10Eye colorHPOID:0000478DOID:240AintronGWASdb_trait
2138494918rs6517404GArs65174048.90E-04Alzheimer's diseaseHPOID:0002511DOID:10652GintronGWASdb_trait
2138517264rs2018521TCrs20185219.90E-04Type 2 diabetes and 6 quantitative traitsHPOID:0005978DOID:9352AintronGWASdb_trait
2138539119rs2244185AGrs22441851.40E-04Type 2 diabetes and 6 quantitative traitsHPOID:0005978DOID:9352GintronGWASdb_trait
2138549236rs2040125AGrs20401257.77E-04Alzheimer's diseaseHPOID:0002511DOID:10652GintronGWASdb_trait
2138549303rs2040126CArs20401263.11E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000182670.13 TTC3 602259