SEC13
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
310344111rs696220GArs6962201.10E-05Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
310351830rs35668GArs356687.06E-05Prion diseasesHPOID:0004429DOID:649AintronGWASdb_trait
310355584rs154238CGrs1542387.26E-05Serum metabolitesHPOID:0011111NACintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000157020.17 SEC13 600152