LTN1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
2130347990rs2255564TCrs22555649.17E-05SchizophreniaHPOID:0100753DOID:5419TintronGWASdb_trait
2130354112rs2832149CTrs28321493.44E-04Type 2 diabetesHPOID:0005978DOID:9352CintronGWASdb_trait
2130357163rs2245431GTrs22454317.91E-05SchizophreniaHPOID:0100753DOID:5419Gcds-synonGWASdb_trait
2130359993rs2832151GTrs28321512.69E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000198862.13 LTN1 613083