STK38L, serine/threonine kinase 38 like, 23012

N. diseases: 12; N. variants: 3
Disease: Glioma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0017638
Disease: Glioma
Glioma 		0.110 GeneticVariation disease BEFREE In addition to confirming two associations reported in other ancestry groups, this study identified one new risk-associated locus for glioma on chromosome 12p11.23 (rs10842893, p<sub>meta</sub> = 2.33x10-12, STK38L) as well as a promising association at 15q15-21.1 (rs4774756, p<sub>meta</sub> = 6.12x10-8, RAB27A) in 3,097 glioma cases and 4,362 controls. 30714141 2019
CUI: C0017638
Disease: Glioma
Glioma 		0.110 GeneticVariation disease GWASCAT Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility. 30714141 2019