Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 215570 single nucleotide variant NM_024907.6(FBXO17):c.644C>A (p.Ser215Ter) 151153509 MedGen:CN169374 19 38945018 38945018 G T 215570 single nucleotide variant NM_024907.6(FBXO17):c.644C>A (p.Ser215Ter) 151153509 MedGen:CN169374 19 39435658 39435658 G T

Disease associated variation - GWASdb Chr Pos SNP ID(dbSNP 142) Ref Alt Ori SNP ID P-value Drug Name Drug Anno GWAS Trait HPO ID DO ID AA Type Trait or Drug 19 39435485 rs10416055 G A rs10416055 4.93E-04 Lung function (forced vital capacity) HPOID:0002088 DOID:850 A intron GWASdb_trait 19 39449411 rs10402813 T G rs10402813 6.03E-05 Body Mass Index HPOID:0001507 DOID:9970 T intron GWASdb_trait 19 39455534 rs12151188 T C rs12151188 3.77E-04 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait