NXF1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1162572433rs3763851CArs37638513.27E-04Alzheimer's disease (late onset)HPOID:0002511DOID:10652CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000162231.13 NXF1 602647