CHD3
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
177811998rs4239111TCrs42391113.66E-05Information processing speedHPOID:0100753|HPOID:0000716DOID:1561CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000170004.16 CHD3 602120