SYMPK, symplekin, 8189

N. diseases: 39; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.110 GeneticVariation disease GWASCAT Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans. 28295283 2017
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.110 GeneticVariation disease BEFREE We identified a novel variant, rs56848936 in the gene SYMPK at 19q13.3, associated with colon cancer risk (odds ratio 0.61 for the risk allele G, p = 2.4 × 10<sup>-8</sup> ). 28295283 2017