PACSIN1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
634458533rs4713797AGrs47137979.36E-04Alcohol consumption (maxi-drinks)HPOID:0000707DOID:1574|DOID:0050741AintronGWASdb_trait
634474629rs4713806CTrs47138063.48E-04Alcohol consumption (maxi-drinks)HPOID:0000707DOID:1574|DOID:0050741CintronGWASdb_trait
634480637rs10947508CTrs109475088.75E-04Type 2 diabetesHPOID:0005978DOID:9352CintronGWASdb_trait
634481092rs3800472GArs38004724.27E-05QT intervalHPOID:0012232|HPOID:0001657DOID:10273|DOID:2843CintronGWASdb_trait
634481140rs3800471TGrs38004711.25E-05Parent of origin effect on language impairment (paternal)HPOID:0002463DOID:93CintronGWASdb_trait
634482267rs11753634CArs117536346.32E-05Parent of origin effect on language impairment (paternal)HPOID:0002463DOID:93AintronGWASdb_trait
634482498rs11758326AGrs117583262.18E-05Parent of origin effect on language impairment (paternal)HPOID:0002463DOID:93GintronGWASdb_trait
634483015rs4713808TCrs47138085.11E-05Erythrocyte countsHPOID:0001627|HPOID:0001871DOID:74|DOID:114CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000124507.10 PACSIN1 606512