PACSIN2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
2243266247rs753086GArs7530867.14E-05Smoking initiationHPOID:0000707DOID:0050742CUTR-3GWASdb_trait
2243278148rs5759010CTrs57590102.02E-04Smoking initiationHPOID:0000707DOID:0050742CintronGWASdb_trait
2243283082rs2267462CTrs22674627.58E-04Smoking initiationHPOID:0000707DOID:0050742CintronGWASdb_trait
2243289236rs2076157CTrs20761577.73E-05Smoking initiationHPOID:0000707DOID:0050742CintronGWASdb_trait
2243289738rs2076158CTrs20761583.31E-04Smoking initiationHPOID:0000707DOID:0050742CintronGWASdb_trait
2243299878rs2267465GArs22674651.58E-04Smoking initiationHPOID:0000707DOID:0050742GintronGWASdb_trait
2243306541rs2267470AGrs22674702.22E-04Smoking initiationHPOID:0000707DOID:0050742GintronGWASdb_trait
2243325441rs2284094AGrs22840942.80E-04Smoking initiationHPOID:0000707DOID:0050742GintronGWASdb_trait
2243347186rs10483216GArs104832166.50E-05Smoking initiationHPOID:0000707DOID:0050742GintronGWASdb_trait
2243366830rs11090130TCrs110901303.53E-05Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
2243372372rs7511534TCrs75115342.30E-11Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287TintronGWASdb_trait
2243390319rs2018340GArs20183405.56E-05Smoking initiationHPOID:0000707DOID:0050742CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000100266.18 PACSIN2 604960