RNF8
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
637329800rs13203701AGrs132037013.24E-05Glucose levelsHPOID:0000819DOID:9352AintronGWASdb_trait
637333318rs195386GArs1953861.90E-04Blood pressureHPOID:0011025DOID:10763TintronGWASdb_trait
637333796rs195385CTrs1953857.32E-04StrokeHPOID:0001297DOID:6713AintronGWASdb_trait
637345704rs195379TCrs1953797.90E-05Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000112130.16 RNF8 611685