SOCS6
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1867960404rs713129GCrs7131292.55E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
1867960594rs713130AGrs7131303.42E-06Eosinophil countsHPOID:0001879|HPOID:0001658|HPOID:0002099DOID:999|DOID:2841|DOID:5844TintronGWASdb_trait
1867981861rs7242186GArs72421868.80E-04Alcohol dependenceHPOID:0000707DOID:0050741GintronGWASdb_trait
1867991256rs2231555CTrs22315550.000000329Cholesterol, totalHPOID:0003107DOID:3393|DOID:3146|DOID:2349CintronGWASdb_trait
1867991256rs2231555CTrs22315557.84E-08HDL cholesterolHPOID:0003107DOID:14502|DOID:1461|DOID:3393CintronGWASdb_trait
1867992432rs2231563CTrs22315635.10E-05Multiple complex diseasesHPOID:0000118NACcds-synonGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000170677.5 SOCS6 605118