MED16
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
19881413rs2365702AGrs23657025.85E-04Amyotrophic Lateral SclerosisHPOID:0007354DOID:332GintronGWASdb_trait
19885818rs1060442AGrs10604426.54E-04Stroke (pediatric)HPOID:0001297DOID:6713Ccds-synonGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000175221.14 MED16 604062