Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6749447
rs6749447
STK39
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 GeneticVariation BEFREE However, the TT genotype ratio in rs6749447</span> was lower in hypertensives (5.4% vs 10.8%, P < 0.05), and the hypertension</span> risk for the TT genotype carriers in rs6749447 decreased after adjustment (OR 0.49, 95% CI 0.19-0.95, P < 0.05). 28945285

2018
dbSNP: rs6749447
rs6749447
STK39
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 GeneticVariation BEFREE Overall analyses failed to see any significant associations of rs6749447, rs35929607 and rs3754777 with hypertension risk (odds ratio: 1.27, 0.95 and 1.21; P = 0.270, 0.507 and 0.153, respectively), and there was evident heterogeneity for three comparisons (I(2) > 80%). 27142475

2016
dbSNP: rs6749447
rs6749447
STK39
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 GeneticVariation BEFREE In conclusion, there was a significant association between STK39 genetic variant rs6749447 and hypertension in a Finnish cohort. 23235358

2013