RFWD2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1175930886rs1357338AGrs13573389.15E-05Bipolar disorder and schizophreniaHPOID:0007302|HPOID:0100753DOID:3312|DOID:5419CintronGWASdb_trait
1175930937rs1357337CTrs13573376.91E-05Elbow painHPOID:0001627DOID:114AintronGWASdb_trait
1175932662rs6704250GCrs67042503.00E-05Bipolar disorder and schizophreniaHPOID:0007302|HPOID:0100753DOID:3312|DOID:5419CintronGWASdb_trait
1176014340rs4622022CArs46220225.61E-04Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
1176027978rs12033847CTrs120338472.68E-05HIV-1 controlHPOID:0002721DOID:526CintronGWASdb_trait
1176043797rs2502826CTrs25028266.91E-05Elbow painHPOID:0001627DOID:114TintronGWASdb_trait
1176044121rs2481653ACrs24816535.65E-05Bipolar disorder and schizophreniaHPOID:0007302|HPOID:0100753DOID:3312|DOID:5419GintronGWASdb_trait
1176092167rs2481627TGrs24816275.71E-05Elbow painHPOID:0001627DOID:114CintronGWASdb_trait
1176172795rs10913150GTrs109131506.91E-05Elbow painHPOID:0001627DOID:114GintronGWASdb_trait
Disease associated variation - GWAS Central
Study NameSource Marker AccessionChromosomeMarker StartMarker StopAllelesGene SectionP-value-log(p-value)
GWAS of prostate cancerrs75549131176008112176008112intronic0.9005110.04551097778045769
GWAS of prostate cancerrs121320721175996304175996304intronic0.8789990.056011619004418
GWAS of prostate cancerrs28616301176042385176042385intronic0.8665080.0622274233253478
GWAS of prostate cancerrs109131501176172795176172795intronic0.8392580.0761045102654775
GWAS of prostate cancerrs25028261176043797176043797intronic0.8212490.0855251462537717
GWAS of prostate cancerrs13573371175930937175930937intronic0.8125740.0901370779450952
GWAS of prostate cancerrs24816271176092167176092167intronic0.7401920.130655613073156
GWAS of prostate cancerrs24871441176148542176148542intronic0.5935240.226561715029816
GWAS of prostate cancerrs24816411176058782176058782intronic0.5227270.281725067057079
GWAS of prostate cancerrs46521431175983994175983994intronic0.2482180.605166728005604
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000143207.19 RFWD2 608067