TRIM69
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1545049695rs2084835TCrs20848352.50E-05Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
1545056132rs3100141TCrs31001415.07E-04Amyotrophic lateral sclerosis (sporadic)HPOID:0007354DOID:332TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000185880.12 TRIM69 616017