CHD5
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
16177202rs7531562GTrs75315625.66E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
16222501rs731975CArs7319754.80E-05Cognitive functionHPOID:0100543DOID:1561TintronGWASdb_trait
Disease associated variation - GWAS Central
Study NameSource Marker AccessionChromosomeMarker StartMarker StopAllelesGene SectionP-value-log(p-value)
GWAS of prostate cancerrs2250358161968696196869exonic0.6301810.20053469497279003
GWAS of prostate cancerrs1883604162128706212870intronic0.5806050.236119228471518
GWAS of prostate cancerrs2281303161703536170353intronic0.5464890.262418575319731
GWAS of prostate cancerrs747393162219756221975intronic0.5084230.293774811093748
GWAS of prostate cancerrs2843493161840926184092exonic0.3692590.432668910768339
GWAS of prostate cancerrs9435102162042666204266intronic0.272070.5653193433828579
GWAS of prostate cancerrs11121407162335736233573intronic0.0884991.0530616366121799
GWAS of prostate cancerrs11121299161940186194018intronic0.0445081.3515619206237701
GWAS of prostate cancerrs2273032162022456202245exonic0.041971.37706103078851
GWAS of prostate cancerrs1883767161754896175489intronic0.003522.4534573365218697
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000116254.17 CHD5 610771