Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35929607
rs35929607
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: rs35929607
rs35929607
STK39
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 GeneticVariation BEFREE A replication study provided supporting evidence that STK39 functional polymorphism rs35929607 was associated with hypertension. 23151749

2013
dbSNP: rs35929607
rs35929607
STK39
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 GeneticVariation BEFREE Our results from two large cohort studies support previous evidence about the association of the STK39 rs35929607A>G variant with hypertension, especially in women. 21178783

2011